chr10_68924081_r_100 100 JDP1 NM_021800 INTRON OMIM: 606060 JDP1 J domain-containing protein 1 chr10_78949952_r_100 100 DLG5 NM_004747 INTRON OMIM: 604090 DLG5, PDLG, KIAA0583 Discs large, Drosophila, homolog of, 5 chr11_19930292_y_100 100 NAV2 NM_145117 INTRON OMIM: 607026 NAV2, RAINB1, KIAA14 Neuron navigator 2 chr11_88813220_y_100 100 NOX4 NM_016931 INTRON OMIM: 605261 NOX4, RENOX NADPH oxidase 4 chr14_50571671_y_100 100 CGI-99 NM_016039 UTR chr14_76020615_r_100 100 SPTLC2 NM_004863 INTRON chr14_89439986_r_100 100 RPS6KA5 NM_004755 INTRON OMIM: 603607 RPS6KA5, MSK1 Ribosomal protein S6 kinase, 90kD, 5 chr14_89439986_r_100 100 RPS6KA5 NM_182398 INTRON OMIM: 603607 RPS6KA5, MSK1 Ribosomal protein S6 kinase, 90kD, 5 chr15_25718168_r_100 100 OCA2 NM_000275 INTRON OMIM: 120436 MLH1, COCA2, HNPCC2 mutL, E. coli, homolog of, 1 Colorectal cancer, hereditary nonpolyposis, type 2, 114500 (3);Turcot syndrome w chr15_38646442_r_100 100 AF15Q14 NM_170589 INTRON chr15_38646442_r_100 100 AF15Q14 NM_144508 INTRON chr16_24839597_r_100 100 KST1 NM_052944 INTRON chr16_66600419_r_100 100 FLJ35894 NM_173616 INTRON chr16_72738276_r_100 100 ATBF1 NM_006885 INTRON OMIM: 104155 ATBF1 AT motif-binding factor 1 MOUSE: 8(Atbf1) chr17_16361942_r_100 100 PIGL NM_004278 INTRON OMIM: 605947 PIGL Phosphatidylinositol glycan, class L chr19_13296838_y_100 100 CACNA1A NM_000068 INTRON OMIM: 601011 CACNA1A, CACNL1A4, S Calcium channel, voltage-dependent, P/Q type, alpha 1A subunit Hemiplegic migraine, familial, 141500 (3); Episodic ataxia, type 2,108500 (3); S MOUSE: 8(tg, Cacl1a4) chr19_13296838_y_100 100 CACNA1A NM_023035 INTRON OMIM: 601011 CACNA1A, CACNL1A4, S Calcium channel, voltage-dependent, P/Q type, alpha 1A subunit Hemiplegic migraine, familial, 141500 (3); Episodic ataxia, type 2,108500 (3); S MOUSE: 8(tg, Cacl1a4) chr19_16908773_y_100 100 VIP NM_015692 INTRON OMIM: 192321 VIPR1 Vasoactive intestinal peptide receptor 1 incorrectly assigned to 2q37 MOUSE: 9(Vipr1) chr19_35597919_y_100 100 KIAA0390 NM_014717 UTR chr1_113691546_r_100 100 PTPN22 NM_015967 INTRON OMIM: 606986 PTPN22, LYP Protein tyrosine phosphatase, nonreceptor-type, 22 chr1_113691546_r_100 100 PTPN22 NM_012411 INTRON OMIM: 606986 PTPN22, LYP Protein tyrosine phosphatase, nonreceptor-type, 22 chr1_154114897_y_100 100 FLJ32884 NM_144702 INTRON chr1_204095767_y_100 100 IL19 NM_153758 INTRON OMIM: 605687 IL19 Interleukin 19 chr1_204095767_y_100 100 IL19 NM_013371 INTRON OMIM: 605687 IL19 Interleukin 19 chr1_97706635_r_100 100 DPYD NM_000110 INTRON OMIM: 274270 DPYD, DPD Dihydropyrimidine dehydrogenase Thymine-uraciluria (3); {Fluorouracil toxicity, sensitivity to} (3) chr20_17633197_r_100 100 RRBP1 NM_004587 INTRON OMIM: 601418 RRBP1, ES130 Ribosome binding protein-1 chr20_19198361_y_100 100 SLC24A3 NM_020689 INTRON chr20_31392082_y_100 100 HCK NM_002110 INTRON OMIM: 142370 HCK Hemopoietic cell kinase chr20_59228178_y_100 100 CDH26 NM_177980 INTRON chr21_31718375_y_100 100 TIAM1 NM_003253 UTR OMIM: 600687 TIAM1 T-cell lymphoma invasion and metastasis 1 MOUSE: 16(Tiam1) chr22_31399095_y_100 100 SYN3 NM_003490 INTRON OMIM: 602705 SYN3 Synapsin III ?relation to schizophrenia chr22_31399095_y_100 100 SYN3 NM_133632 INTRON OMIM: 602705 SYN3 Synapsin III ?relation to schizophrenia chr22_31399095_y_100 100 SYN3 NM_133633 INTRON OMIM: 602705 SYN3 Synapsin III ?relation to schizophrenia chr2_122434990_r_100 100 CLASP1 NM_015282 INTRON OMIM: 605852 CLASP1, KIAA0622 CLIP-associated protein 1 chr2_27870699_y_100 100 SLC4A1AP NM_018158 INTRON OMIM: 602655 SLC4A1AP Solute carrier family 4 (anion exchanger), member 1, adaptor protein chr2_27870800_y_100 100 SLC4A1AP NM_018158 INTRON OMIM: 602655 SLC4A1AP Solute carrier family 4 (anion exchanger), member 1, adaptor protein chr2_40593824_r_100 100 SLC8A1 NM_021097 INTRON OMIM: 182305 SLC8A1, NCX1 Solute carrier family 8, member 1 (sodium-calcium exchanger-1) chr3_125325810_y_100 100 HAPIP NM_003947 INTRON chr3_175184792_y_100 100 NLGN1 NM_014932 INTRON OMIM: 600568 NLGN1 Neuroligin 1 chr3_193197335_y_100 100 FGF12 NM_021032 INTRON OMIM: 601513 FGF12, FHF1 Fibroblast growth factor-12 MOUSE: 16(Fhf1) chr3_193197335_y_100 100 FGF12 NM_004113 INTRON OMIM: 601513 FGF12, FHF1 Fibroblast growth factor-12 MOUSE: 16(Fhf1) chr4_20937931_y_100 100 KCNIP4 NM_147183 INTRON OMIM: 608182 KCNIP4, KCHIP4 Kv channel-interacting protein 4 chr4_20937931_y_100 100 KCNIP4 NM_147182 UTR OMIM: 608182 KCNIP4, KCHIP4 Kv channel-interacting protein 4 chr4_26409461_y_100 100 FLJ11082 NM_018317 INTRON chr4_2702102_y_100 100 C4orf8 NM_003704 INTRON chr4_77256904_r_100 100 PPEF2 NM_006239 INTRON OMIM: 602256 PPEF2 Protein phsophatase, EF hand calcium-binding domain-2 chr4_77256904_r_100 100 PPEF2 NM_152933 INTRON OMIM: 602256 PPEF2 Protein phsophatase, EF hand calcium-binding domain-2 chr4_77256904_r_100 100 PPEF2 NM_152934 UTR OMIM: 602256 PPEF2 Protein phsophatase, EF hand calcium-binding domain-2 chr4_86015174_y_100 100 CDS1 NM_001263 INTRON OMIM: 603548 CDS1 CDP-diacylglycerol synthase 1 chr5_95153784_y_100 100 RHOBTB3 NM_014899 INTRON OMIM: 607353 RHOBTB3, KIAA0878 Rho-related BTB domain-containing protein 3 chr6_128494584_r_100 100 PTPRK NM_002844 INTRON OMIM: 602545 PTPRK Protein-tyrosine phosphatase, receptor type, kappa MOUSE: 10(Ptprk) chr6_34381054_r_100 100 NUDT3 NM_006703 INTRON chr6_36296808_r_100 100 PNPLA1 NM_173676 UTR chr6_37992457_y_100 100 TEX27 NM_021943 INTRON chr6_46812334_y_100 100 MEP1A NM_005588 INTRON OMIM: 600388 MEP1A Meprin A, alpha MOUSE: 17(Mep1a) chr6_56088231_r_100 100 COL21A1 NM_030820 INTRON chr6_69806396_r_100 100 BAI3 NM_001704 INTRON OMIM: 602684 BAI3 Brain-specific angiogenesis inhibitor-3 chr8_107641296_r_100 100 OXR1 NM_181354 UTR OMIM: 605609 OXR1 Oxidation resistance 1 ?pseudogene on chr.15 chr8_2972828_r_100 100 CSMD1 NM_033225 INTRON OMIM: 608397 CSMD1, KIAA1890 Cub and Sushi multiple domains 1 chr9_113388543_r_100 100 DEC1 NM_017418 UTR OMIM: 606393 ADAMDEC1, DECYSIN A disintegrin and metalloproteinase domain-like protein decysin 1 chrX_103745711_r_100 100 IL1RAPL2 NM_017416 INTRON OMIM: 300277 IL1RAPL2 Interleukin 1 receptor accessory protein-like 2 chrX_127955242_r_100 100 RAB33A NM_004794 UTR OMIM: 300333 RAB33A Ras-associated protein RAB33A chrX_21107717_y_100 100 SMPX NM_014332 UTR OMIM: 300226 SMPX Small muscle protein, X-linked chrX_83940176_r_100 100 CHM NM_000390 INTRON OMIM: 139340 GNAT2, ACHM4 Guanine nucleotide-binding protein (G-protein), alpha-transducing(transducin) ac Achromatopsia-4 (3) MOUSE: 3(Gnat2) chrX_83940176_r_100 100 FLJ38564 NM_152579 UTR chrX_95622410_y_100 100 DIAPH2 NM_006729 INTRON OMIM: 300108 DIAPH2, DIA, POF2 Diaphanous, Drosophila, homolog of, 2 Premature ovarian failure, 311360 (3) chr10_125835617_r_101 101 LHPP NM_022126 INTRON chr10_17932296_y_101 101 MRC1 NM_002438 INTRON OMIM: 153618 MRC1 Mannose receptor, C type 1 MOUSE: 2(Mrc1) chr10_18179215_y_101 101 MRC1 NM_002438 INTRON OMIM: 153618 MRC1 Mannose receptor, C type 1 MOUSE: 2(Mrc1) chr10_28372994_r_101 101 FLJ32798 NM_173496 INTRON chr10_70034395_y_101 101 DDX50 NM_024045 INTRON chr11_113334821_y_101 101 HTR3B NM_006028 INTRON OMIM: 604654 HTR3B 5-hydroxytryptamine receptor 3B chr11_659650_r_101 101 SIRT3 NM_012239 UTR OMIM: 604481 SIRT3, SIR2L3 Sirtuin, S. cerevisiae, homolog 3 chr11_659650_r_101 101 DEAF1 NM_021008 INTRON chr11_68232150_y_101 101 GAL NM_015973 INTRON OMIM: 606953 GALE UDP galactose-4-epimerase Galactose epimerase deficiency, 230350 (3) chr12_80100518_y_101 101 FLJ21963 NM_024560 INTRON chr13_46832024_y_101 101 RB1 NM_000321 INTRON OMIM: 604210 CRB1, RP12 Crumbs, Drosophila, homolog of, 1 Retinitis pigmentosa-12, autosomal recessive, 600105 (3);Leber congenital amauro chr13_90071299_y_101 101 GPC5 NM_004466 INTRON OMIM: 602446 GPC5 Glypican 5 chr14_65586515_r_101 101 GPHN NM_020806 INTRON chr14_67864018_y_101 101 FLJ11274 NM_018375 INTRON chr14_76297249_r_101 101 ADCK1 NM_020421 INTRON chr15_97123960_y_101 101 IGF1R NM_000875 INTRON OMIM: 147370 IGF1R Insulin-like growth factor-1 receptor Intrauterine and postnatal growth retardation (3) MOUSE: 7(Igf1r) chr16_50031655_y_101 101 TRF4-2 NM_022447 UTR chr17_56747914_y_101 101 EPX NM_000502 INTRON OMIM: 606216 SEPX1, SELX Selenoprotein X, 1 chr17_75755052_y_101 101 SEC14L1 NM_003003 INTRON chr19_53480594_r_101 101 MGC17986 NM_153608 INTRON chr19_55687745_r_101 101 NR1H2 NM_007121 UTR OMIM: 600380 NR1H2, UNR Nuclear receptor subfamily 1, group H, member 2(ubiquitously-expressed nuclear r chr1_119930838_r_101 101 NOTCH2 NM_024408 INTRON OMIM: 600275 NOTCH2 Notch, Drosophila, homolog of, 2 MOUSE: 3(Notch2) chr1_142985574_y_101 101 LOC64182 NM_022359 UTR chr1_152298022_y_101 101 MUC1 NM_182741 UTR OMIM: 158340 MUC1, PUM Mucin 1, transmembrane 5cM proximal to SPTA1 MOUSE: 3(Muc1) chr1_21348043_y_101 101 ALPL NM_000478 UTR OMIM: 171760 ALPL, HOPS, TNSALP Alkaline phosphatase, liver/bone/kidney Hypophosphatasia, infantile, 241500 (3); Hypophosphatasia, childhood,241510 (3); MOUSE: 4(Akp2) chr1_26488925_y_101 101 RPS6KA1 NM_002953 INTRON OMIM: 601684 RPS6KA1, RSK1 Ribosomal protein S6 kinase, 90kD, 1 chr1_39272794_r_101 101 MACF1 NM_012090 INTRON chr1_39272794_r_101 101 MACF1 NM_033044 INTRON chr1_77959764_y_101 101 GIPC2 NM_017655 INTRON chr1_78889432_r_101 101 ELTD1 NM_022159 UTR chr22_44782315_r_101 101 PPARA NM_005036 UTR OMIM: 170998 PPARA, PPAR Peroxisome proliferator-activated receptor-alpha chr2_166658302_r_101 101 TAIP-2 NM_024969 INTRON chr2_178727303_y_101 101 PDE11A NM_016953 INTRON chr3_89429476_y_101 101 EPHA3 NM_005233 INTRON OMIM: 179611 EPHA3, ETK1, HEK Ephrin receptor EphA3 (human embryo kinase 1) chr4_15747847_r_101 101 PROM1 NM_006017 INTRON OMIM: 604365 PROM1, PROML1, AC133 Prominin 1 Retinal degeneration, autosomal recessive, prominin-related (3) chr4_16334465_r_101 101 LDB2 NM_001290 INTRON OMIM: 603450 LDB2, CLIM1 LIM domain-binding factor-2 chr4_185779546_r_101 101 MGC33971 NM_153343 INTRON chr4_3392265_y_101 101 RGS12 NM_002926 INTRON chr4_96349781_y_101 101 BMPR1B NM_001203 UTR OMIM: 603248 BMPR1B, ALK6 Bone morphogenetic protein receptor, type IB chr5_141379624_y_101 101 RNF14 NM_004290 UTR OMIM: 605675 RNF14, ARA54 RING finger protein-14 chr6_106745137_r_101 101 APG5L NM_004849 INTRON OMIM: 604261 APG5L Autophagy 5, S. cerevisiae, homolog of chr6_124779436_y_101 101 TCBA1 NM_153355 INTRON chr6_129588767_r_101 101 LAMA2 NM_000426 INTRON OMIM: 156225 LAMA2, LAMM Laminin, alpha-2 (merosin) Muscular dystrophy, congenital merosin-deficient, 607855 (3);Muscular dystrophy, MOUSE: 10(dy, Lamm) chr6_70480439_r_101 101 FLJ11240 NM_018368 INTRON chr7_101030685_y_101 101 CUTL1 NM_001913 INTRON OMIM: 116896 CUTL1, CDP Cut, Drosophila, homolog of (CCAAT displacement protein) chr7_101030685_y_101 101 CUTL1 NM_181500 INTRON OMIM: 116896 CUTL1, CDP Cut, Drosophila, homolog of (CCAAT displacement protein) chr7_101030685_y_101 101 CUTL1 NM_181552 INTRON OMIM: 116896 CUTL1, CDP Cut, Drosophila, homolog of (CCAAT displacement protein) chr7_111127411_r_101 101 DOCK4 NM_014705 INTRON OMIM: 607679 DOCK4, KIAA0716 Dedicator of cytokinesis 4 MOUSE: 12(Dock4) chr7_126101798_r_101 101 GRM8 NM_000845 INTRON OMIM: 601116 GRM8 Glutamate receptor, metabotropic-8 chr7_129460578_y_101 101 CPA2 NM_001869 INTRON OMIM: 600688 CPA2 Carboxypeptidase A2, pancreatic chr7_132113761_r_101 101 FLJ20420 NM_017812 INTRON chr7_145577066_y_101 101 CNTNAP2 NM_014141 INTRON OMIM: 604569 CNTNAP2, CASPR2, NRX Contactin-associated protein-like 2 chr7_147013950_r_101 101 CNTNAP2 NM_014141 INTRON OMIM: 604569 CNTNAP2, CASPR2, NRX Contactin-associated protein-like 2 chr7_28333857_y_101 101 H_GS165L15.1 NM_004904 INTRON chr7_37977513_y_101 101 STARD3NL NM_032016 UTR chr7_90136824_y_101 101 PFTK1 NM_012395 INTRON chr8_104803484_y_101 101 RIMS2 NM_014677 INTRON OMIM: 606630 RIMS2, KIAA0751, RIM Regulating synaptic membrane exocytosis-2 chr8_11399246_r_101 101 BLK NM_001715 UTR OMIM: 191305 BLK BLK nonreceptor tyrosine kinase MOUSE: 14(Blk) chr8_4355744_y_101 101 CSMD1 NM_033225 INTRON OMIM: 608397 CSMD1, KIAA1890 Cub and Sushi multiple domains 1 chr8_62302203_r_101 101 MGC34646 NM_173519 INTRON chr8_87090325_r_101 101 ATP6V0D2 NM_152565 INTRON chrX_107488231_r_101 101 GUCY2F NM_001522 UTR OMIM: 300041 GUCY2F, GUC2F Guanylate cyclase 2F MOUSE: X(Gucy2f) chrX_122519797_y_101 101 ODZ1 NM_014253 INTRON chrX_32616703_y_101 101 DMD NM_000109 INTRON OMIM: 605512 ELOVL4, ADMD, STGD2, Elongation of very long chain fatty acids 4 Stargardt disease 3, 600110 (3); Macular dystrophy, autosomaldominant, chromosom chrX_73563318_y_101 101 ZDHHC15 NM_144969 INTRON chr11_122107860_y_102 102 KIAA1959 NM_032873 INTRON chr11_21091651_y_102 102 NELL1 NM_006157 INTRON OMIM: 602319 NELL1 Nel-like 1 chr11_9928704_r_102 102 CMT4B2 NM_030962 INTRON OMIM: 607697 SBF2, MTMR13, CMT4B2 SET binding factor 2 (myotubularin-related 13) Charcot-Marie-Tooth disease, type 4B2, 604563 (3);Charcot-Marie-Tooth disease, t chr12_94789647_y_102 102 FLJ40089 NM_182496 INTRON chr13_90929493_y_102 102 GPC5 NM_004466 INTRON OMIM: 602446 GPC5 Glypican 5 chr15_30113696_r_102 102 CHRNA7 NM_000746 INTRON OMIM: 118511 CHRNA7 Cholinergic receptor, nicotinic, alpha polypeptide-7 Schizophrenia, neurophysiologic defect in (2) MOUSE: 7(Acra7) chr15_55472920_y_102 102 FLJ14957 NM_032866 INTRON chr15_88117193_y_102 102 AP3S2 NM_005829 INTRON chr16_68553371_y_102 102 CDH1 NM_004360 INTRON OMIM: 608286 PCDH10, KIAA1400 Protocadherin 10 chr17_72889572_r_102 102 DNAI2 NM_023036 INTRON OMIM: 605483 DNAI2 Dynein, axonemal, intermediate chain 2 chr17_9668170_r_102 102 STX8 NM_004853 INTRON OMIM: 604203 STX8 Syntaxin 8 chr19_50509197_r_102 102 CKM NM_001824 INTRON OMIM: 123295 CKMT2 Creatine kinase, mitochondrial-2 (sarcomeric) chr19_7201168_r_102 102 INSR NM_000208 INTRON OMIM: 147671 INSRR, IRR Insulin receptor-related receptor chr1_111435852_r_102 102 RAP1A NM_002884 UTR OMIM: 179520 RAP1A, KREV1 RAS-related protein RAP1A pseudogene on 14q24.3 chr1_147784778_r_102 102 MCL1 NM_021960 UTR OMIM: 159552 MCL1 Myeloid cell leukemia sequence 1 (BCL2-related) MOUSE: 3(Mcl1) chr1_197894217_y_102 102 DKFZP564B1023 NM_031306 INTRON chr1_214801768_r_102 102 FLJ10252 NM_018040 INTRON chr1_54218577_r_102 102 SSBP3 NM_145716 INTRON OMIM: 607390 SSBP3 Single-stranded DNA-binding protein 3 chr1_54218577_r_102 102 SSBP3 NM_018070 INTRON OMIM: 607390 SSBP3 Single-stranded DNA-binding protein 3 chr1_66708750_y_102 102 FLJ23129 NM_024763 INTRON chr22_16441713_r_102 102 SLC25A18 NM_031481 INTRON chr22_37627705_y_102 102 APOBEC3B NM_004900 INTRON OMIM: 607110 APOBEC3B, PHRBNL Apolipoprotein B mRNA editing enzyme, catalytic polypeptide-like 3B chr2_144350395_y_102 102 ARHGAP15 NM_018460 INTRON chr2_202904570_r_102 102 ALS2CR7 NM_139158 INTRON chr2_203451777_y_102 102 BMPR2 NM_001204 INTRON OMIM: 600799 BMPR2, PPH1 Bone morphogenetic receptor, type II Pulmonary hypertension, familial primary, 178600 (3) chr2_203451777_y_102 102 BMPR2 NM_033346 INTRON OMIM: 600799 BMPR2, PPH1 Bone morphogenetic receptor, type II Pulmonary hypertension, familial primary, 178600 (3) chr2_215193247_y_102 102 PF20 NM_024532 INTRON chr2_231821628_y_102 102 MO25 NM_016289 UTR chr3_193416721_y_102 102 FGF12 NM_021032 INTRON OMIM: 601513 FGF12, FHF1 Fibroblast growth factor-12 MOUSE: 16(Fhf1) chr3_193416721_y_102 102 FGF12 NM_004113 INTRON OMIM: 601513 FGF12, FHF1 Fibroblast growth factor-12 MOUSE: 16(Fhf1) chr3_51687043_y_102 102 ZSIG11 NM_015926 INTRON chr4_1860069_y_102 102 WHSC1 NM_007331 UTR OMIM: 602952 WHSC1 Wolf-Hirschhorn syndrome candidate 1 chr4_1860069_y_102 102 WHSC1 NM_014919 UTR OMIM: 602952 WHSC1 Wolf-Hirschhorn syndrome candidate 1 chr4_1860069_y_102 102 WHSC1 NM_133330 UTR OMIM: 602952 WHSC1 Wolf-Hirschhorn syndrome candidate 1 chr4_1860069_y_102 102 WHSC1 NM_133331 UTR OMIM: 602952 WHSC1 Wolf-Hirschhorn syndrome candidate 1 chr4_1860069_y_102 102 WHSC1 NM_133332 UTR OMIM: 602952 WHSC1 Wolf-Hirschhorn syndrome candidate 1 chr4_1860069_y_102 102 WHSC1 NM_133333 UTR OMIM: 602952 WHSC1 Wolf-Hirschhorn syndrome candidate 1 chr4_1860069_y_102 102 WHSC1 NM_133335 UTR OMIM: 602952 WHSC1 Wolf-Hirschhorn syndrome candidate 1 chr4_66364045_r_102 102 EPHA5 NM_004439 INTRON chr4_66364045_r_102 102 EPHA5 NM_182472 INTRON chr5_172504306_y_102 102 LOC153222 NM_153607 INTRON chr5_19639277_y_102 102 CDH18 NM_004934 INTRON OMIM: 608287 PCDH18, KIAA1562 Protocadherin 18 chr6_129510227_r_102 102 LAMA2 NM_000426 INTRON OMIM: 156225 LAMA2, LAMM Laminin, alpha-2 (merosin) Muscular dystrophy, congenital merosin-deficient, 607855 (3);Muscular dystrophy, MOUSE: 10(dy, Lamm) chr6_13518777_r_102 102 GFOD1 NM_018988 INTRON chr6_152716786_r_102 102 SYNE1 NM_033071 INTRON chr6_69980074_y_102 102 BAI3 NM_001704 INTRON OMIM: 602684 BAI3 Brain-specific angiogenesis inhibitor-3 chr7_107633863_r_102 102 NRCAM NM_005010 UTR OMIM: 601581 NRCAM Neuronal cell adhesion molecule chr7_2768442_y_102 102 CARD11 NM_032415 UTR chr8_118827638_r_102 102 EXT1 NM_000127 INTRON OMIM: 608177 EXT1 Exostosin 1 distal to TRPS1 Exostoses, multiple, type 1, 133700 (3); Chondrosarcoma, 215300 (3) MOUSE: 15(Ext1) chr8_120959853_y_102 102 FLJ12428 NM_022783 INTRON chr8_32524725_y_102 102 NRG1 NM_013962 INTRON OMIM: 142445 NRG1, HGL, HRGA, ARI Neuregulin 1 (heregulin, alpha, 45kD; ERBB2 p185-activator) {?Schizophrenia, susceptibility to}, 603013 (1) MOUSE: 7(Nrg1) chr8_32524725_y_102 102 NRG1 NM_013958 INTRON OMIM: 142445 NRG1, HGL, HRGA, ARI Neuregulin 1 (heregulin, alpha, 45kD; ERBB2 p185-activator) {?Schizophrenia, susceptibility to}, 603013 (1) MOUSE: 7(Nrg1) chr8_32524725_y_102 102 NRG1 NM_013957 INTRON OMIM: 142445 NRG1, HGL, HRGA, ARI Neuregulin 1 (heregulin, alpha, 45kD; ERBB2 p185-activator) {?Schizophrenia, susceptibility to}, 603013 (1) MOUSE: 7(Nrg1) chr8_32524725_y_102 102 NRG1 NM_004495 INTRON OMIM: 142445 NRG1, HGL, HRGA, ARI Neuregulin 1 (heregulin, alpha, 45kD; ERBB2 p185-activator) {?Schizophrenia, susceptibility to}, 603013 (1) MOUSE: 7(Nrg1) chr8_32524725_y_102 102 NRG1 NM_013961 INTRON OMIM: 142445 NRG1, HGL, HRGA, ARI Neuregulin 1 (heregulin, alpha, 45kD; ERBB2 p185-activator) {?Schizophrenia, susceptibility to}, 603013 (1) MOUSE: 7(Nrg1) chr8_32524725_y_102 102 NRG1 NM_013964 INTRON OMIM: 142445 NRG1, HGL, HRGA, ARI Neuregulin 1 (heregulin, alpha, 45kD; ERBB2 p185-activator) {?Schizophrenia, susceptibility to}, 603013 (1) MOUSE: 7(Nrg1) chr8_32524725_y_102 102 NRG1 NM_013960 INTRON OMIM: 142445 NRG1, HGL, HRGA, ARI Neuregulin 1 (heregulin, alpha, 45kD; ERBB2 p185-activator) {?Schizophrenia, susceptibility to}, 603013 (1) MOUSE: 7(Nrg1) chr8_32524725_y_102 102 NRG1 NM_013956 INTRON OMIM: 142445 NRG1, HGL, HRGA, ARI Neuregulin 1 (heregulin, alpha, 45kD; ERBB2 p185-activator) {?Schizophrenia, susceptibility to}, 603013 (1) MOUSE: 7(Nrg1) chr8_70747190_r_102 102 SLC21A15 NM_030958 INTRON chr8_87086754_y_102 102 ATP6V0D2 NM_152565 INTRON chrX_134171579_y_102 102 GPR112 NM_153834 INTRON chrX_28886776_y_102 102 IL1RAPL1 NM_014271 INTRON chrX_3162929_r_102 102 PRKX NM_005044 INTRON OMIM: 300083 PRKX Protein kinase, X-linked chrX_42701754_r_102 102 MAOB NM_000898 INTRON OMIM: 309860 MAOB Monoamine oxidase B MOUSE: X(Maob) chrY_23123368_r_102 102 TTTY6 NM_032585 UTR chr10_102443887_y_103 103 FLJ23209 NM_024895 INTRON chr10_122793645_r_103 103 FGFR2 NM_022971 UTR OMIM: 176943 FGFR2, BEK, CFD1, JW Fibroblast growth factor receptor-2 (bacteria-expressed kinase) Crouzon syndrome, 123500 (3); Jackson-Weiss syndrome, 123150 (3);Beare-Stevenson MOUSE: 7(Fgfr2) chr10_20365313_r_103 103 TEM7R NM_032812 INTRON OMIM: 606827 TEM7R Tumor endothelial marker 7-related protein chr11_19183336_y_103 103 CSRP3 NM_003476 UTR OMIM: 600824 CSRP3, CRP3, CLP, CM Cysteine- and glycine-rich protein 3 Cardiomyopathy, dilated, 1M, 607482 (3) chr11_47000564_r_103 103 MGC4707 NM_024113 INTRON chr12_108040782_y_103 103 ACACB NM_001093 INTRON OMIM: 601557 ACACB, ACCB, ACC2 Acetyl-Coenzyme A carboxylase, beta chr12_55247437_r_103 103 RBMS2 NM_002898 INTRON chr12_66904731_r_103 103 IL26 NM_018402 INTRON OMIM: 605679 IL26, AK155 Interleukin 26 chr14_102232518_r_103 103 PPP1R13B NM_015316 INTRON chr14_88534803_r_103 103 KCNK13 NM_022054 INTRON OMIM: 607367 KCNK13, THIK1 Potassium channel, subfamily K, member 13 chr15_55421410_y_103 103 FLJ14957 NM_032866 UTR chr15_71883405_r_103 103 MGC34741 NM_153356 INTRON chr16_4048995_r_103 103 ADCY9 NM_001116 INTRON OMIM: 603302 ADCY9 Adenylate cyclase-9 MOUSE: 16(Adcy9) chr16_70880319_y_103 103 DKFZp434L0850 NM_017558 INTRON chr16_7266783_y_103 103 A2BP1 NM_018723 INTRON chr16_81407114_y_103 103 KIAA1694 NM_030629 INTRON chr17_10457755_r_103 103 MYH13 NM_003802 INTRON OMIM: 603487 MYH13 Myosin, heavy polypeptide 13, skeletal muscle MOUSE: 11(Myh13) chr17_4578590_y_103 103 MGC29671 NM_182538 INTRON chr17_66881168_y_103 103 SLC16A6 NM_004694 UTR chr19_15481662_y_103 103 FLJ39501 NM_173483 UTR chr19_49007660_r_103 103 FLJ30469 NM_182573 UTR chr19_7142299_r_103 103 INSR NM_000208 INTRON OMIM: 147671 INSRR, IRR Insulin receptor-related receptor chr1_154116594_y_103 103 FLJ32884 NM_144702 INTRON chr1_217816883_y_103 103 MARK1 NM_018650 INTRON OMIM: 606511 MARK1, KIAA1477 MAP/microtubule affinity-regulating kinase 1 chr1_227922337_r_103 103 CAPN9 NM_006615 INTRON OMIM: 606401 CAPN9 Calpain 9 chr1_39026020_y_103 103 MACF1 NM_012090 INTRON chr1_71541376_r_103 103 KILON NM_173808 INTRON chr20_19528657_y_103 103 SLC24A3 NM_020689 INTRON chr22_19107047_y_103 103 SCARF2 NM_153334 INTRON chr2_125527111_y_103 103 caspr5 NM_130773 INTRON chr2_125527111_y_103 103 caspr5 NM_138996 INTRON chr2_131212336_y_103 103 PTPN18 NM_014369 INTRON OMIM: 606587 PTPN18, BDP1 Protein-tyrosine phosphatase, nonreceptor-type, 18 chr2_169077553_r_103 103 STK39 NM_013233 INTRON OMIM: 607648 STK39, SPAK Serine/threonine protein kinase 39 chr2_202925596_y_103 103 ALS2CR7 NM_139158 INTRON chr2_27085567_y_103 103 DPYSL5 NM_020134 UTR OMIM: 608383 DPYSL5, CRMP5, CRAM Dihydropyrimidinase-like 5 MOUSE: 5(Dpysl5) chr2_32164816_r_103 103 CGI-27 NM_015955 INTRON chr2_32923291_y_103 103 FLJ20272 NM_017735 INTRON chr2_63221376_r_103 103 KIAA0903 NM_015252 INTRON chr3_101650987_y_103 103 GPR128 NM_032787 INTRON chr3_115517574_y_103 103 ZNF288 NM_015642 UTR chr3_162019364_r_103 103 PP2CE NM_139245 INTRON chr3_184399658_r_103 103 KIAA0861 NM_015078 INTRON chr3_189289386_y_103 103 LPP NM_005578 UTR OMIM: 171800 ALPP Alkaline phosphatase, placental (Regan isozyme) MOUSE: 4(Akp2) chr3_196214876_y_103 103 FLJ35155 NM_152531 INTRON chr5_137666873_r_103 103 GFRA3 NM_001496 INTRON OMIM: 605710 GFRA3 GDNF family receptor alpha-3 chr5_147893057_r_103 103 HTR4 NM_000870 INTRON OMIM: 602164 HTR4 5-hydroxytryptamine (serotonin) receptor-4 chr6_38452794_r_103 103 BTBD9 NM_152733 INTRON chr7_104251590_y_103 103 MLL5 NM_018682 INTRON chr7_55315049_r_103 103 DKFZP564K0822 NM_030796 INTRON chr7_68950110_y_103 103 AUTS2 NM_015570 INTRON OMIM: 607270 AUTS2, KIAA0442 Autism susceptibility gene 2 translocation break at 7q11.2 Autism-like syndrome (2) chr7_73187564_y_103 103 CYLN2 NM_003388 INTRON OMIM: 603432 CYLN2, WBSCR4, WSCR4 Cytoplasmic linker 2 ?neurodevelpmental defect of Williams syndrome MOUSE: 5(Cyln2) chr7_73187564_y_103 103 CYLN2 NM_032421 INTRON OMIM: 603432 CYLN2, WBSCR4, WSCR4 Cytoplasmic linker 2 ?neurodevelpmental defect of Williams syndrome MOUSE: 5(Cyln2) chr7_80031654_r_103 103 SEMA3C NM_006379 INTRON chr7_86831125_r_103 103 ABCB1 NM_000927 INTRON OMIM: 605454 ABCB10, MTABC2 ATP-binding cassette, subfamily B, member 10 pseudogene on 15q13-q14 chr8_40756416_r_103 103 FLJ13842 NM_024645 UTR chr8_60017393_r_103 103 TOX NM_014729 INTRON OMIM: 602270 ATOX1, HAH1 Antioxidant protein 1 (ATX, yeast, homolog of) chr9_103594789_y_103 103 CSDUFD1 NM_031919 INTRON chr9_110298069_r_103 103 DKFZP761E1824 NM_022486 UTR chr9_67712934_r_103 103 APBA1 NM_001163 UTR OMIM: 602414 APBA1, X11 Amyloid beta A4 precursor protein-binding, family A, member 1 chr9_96217513_r_103 103 NANS NM_018946 INTRON OMIM: 605202 NANS, SAS N-acetylneuraminic acid synthase (sialic acid synthase) chrX_14813026_r_103 103 PIR NM_003662 INTRON OMIM: 603092 DUSP11, PIR1 Dual specificity phosphatase-11, RNA/RNP complex-interacting chrX_5598849_y_103 103 NLGN4 NM_020742 UTR OMIM: 300427 NLGN4, KIAA1260 Neuroligin 4 Autism, X-linked, 300425 (3); Asperger syndrome, 300425 (3) chrX_5598849_y_103 103 NLGN4 NM_181332 UTR OMIM: 300427 NLGN4, KIAA1260 Neuroligin 4 Autism, X-linked, 300425 (3); Asperger syndrome, 300425 (3) chrX_95155946_y_103 103 DIAPH2 NM_007309 INTRON OMIM: 300108 DIAPH2, DIA, POF2 Diaphanous, Drosophila, homolog of, 2 Premature ovarian failure, 311360 (3) chrX_95155946_y_103 103 DIAPH2 NM_006729 INTRON OMIM: 300108 DIAPH2, DIA, POF2 Diaphanous, Drosophila, homolog of, 2 Premature ovarian failure, 311360 (3) chr10_1564727_r_104 104 ADARB2 NM_018702 INTRON OMIM: 602065 ADARB2, RED2 Adenosine deaminase, RNA-specific, B2 (homolog of rat BLUE) chr10_45275258_r_104 104 c-MIR NM_145021 INTRON chr10_52629555_r_104 104 PRKG1 NM_006258 INTRON OMIM: 176894 PRKG1, PRKG1B, PRKGR Protein kinase, cGMP-dependent, regulatory, type I chr10_73909523_y_104 104 LOC90550 NM_138357 INTRON chr10_75578826_y_104 104 ADK NM_006721 INTRON OMIM: 600758 PTK2, FADK PTK2 protein tyrosine kinase MOUSE: 15(Fadk) chr10_75578826_y_104 104 ADK NM_001123 INTRON OMIM: 600758 PTK2, FADK PTK2 protein tyrosine kinase MOUSE: 15(Fadk) chr11_123057947_y_104 104 SCN3B NM_018400 INTRON chr12_101311776_y_104 104 IGF1 NM_000618 INTRON OMIM: 147440 IGF1 Insulin-like growth factor-1, or somatomedin C Growth retardation with deafness and mental retardation (3) MOUSE: 10(Igf1) chr12_24188006_r_104 104 SOX5 NM_152989 UTR OMIM: 604975 SOX5 SRY-box 5 MOUSE: 6(Sox5) chr12_48148081_y_104 104 SCR59 NM_023071 INTRON chr13_26723004_y_104 104 FLT1 NM_002019 INTRON OMIM: 165070 FLT1 fms-related tyrosine kinase-1 (vascular endothelial growthfactor/vascular permea 150kb from FLT3 chr13_34354518_r_104 104 DCAMKL1 NM_004734 INTRON OMIM: 604742 DCAMKL1 Doublecortin- and calmodulin kinase-like 1 chr13_75618694_r_104 104 PAM NM_015057 INTRON OMIM: 170270 PAM Peptidylglycine alpha-amidating monooxygenase MOUSE: 1(Pam) chr14_28222593_r_104 104 PRKCM NM_002742 INTRON OMIM: 605435 PRKCM Protein kinase C, mu also assigned to chr.21 chr14_33712577_r_104 104 KIAA0391 NM_014672 INTRON chr14_59809399_r_104 104 PRKCH NM_006255 INTRON OMIM: 605437 PRKCH, PKCL, PRKCL Protein kinase C, eta chr15_89561592_y_104 104 SV2B NM_014848 INTRON chr15_96748171_y_104 104 FLJ39743 NM_182562 INTRON chr16_24295505_r_104 104 CACNG3 NM_006539 INTRON OMIM: 606403 CACNG3 Calcium channel, voltage-dependent, gamma-3 subunit chr16_57739808_r_104 104 CNGB1 NM_001297 INTRON OMIM: 600724 CNGB1, CNCG3L, CNCG2 Cyclic nucleotide gated channel, beta 1 Retinitis pigmentosa, autosomal recessive, 268000 (3) chr16_6169035_y_104 104 A2BP1 NM_018723 UTR chr19_16920753_r_104 104 VIP NM_015692 INTRON OMIM: 192321 VIPR1 Vasoactive intestinal peptide receptor 1 incorrectly assigned to 2q37 MOUSE: 9(Vipr1) chr19_2543985_r_104 104 FLJ00058 NM_052847 UTR chr19_2589397_r_104 104 FLJ00058 NM_052847 UTR chr19_53529567_y_104 104 FLJ10922 NM_018273 INTRON chr19_7100899_r_104 104 INSR NM_000208 INTRON OMIM: 147671 INSRR, IRR Insulin receptor-related receptor chr1_176550769_y_104 104 SOAT1 NM_003101 INTRON chr1_194802161_r_104 104 FLJ20054 NM_019049 INTRON chr1_199949066_r_104 104 SYT2 NM_177402 UTR OMIM: 600104 SYT2 Synaptotagmin-2 ?near REN MOUSE: 1(Syt2) chr1_238767288_r_104 104 KMO NM_003679 INTRON OMIM: 603538 KMO Kynurenine 3-monooxygenase chr1_99994205_y_104 104 HIAT1 NM_033055 INTRON chr20_25012589_r_104 104 ACAS2L NM_032501 INTRON chr20_262169_r_104 104 C20orf96 NM_153269 INTRON chr21_37029503_y_104 104 SIM2 NM_009586 INTRON OMIM: 600892 SIM2 Single-minded, Drosophila, homolog of, 2 chr21_37029503_y_104 104 SIM2 NM_005069 INTRON OMIM: 600892 SIM2 Single-minded, Drosophila, homolog of, 2 chr21_46771291_y_104 104 DIP2 NM_015151 INTRON OMIM: 607711 DIP2, KIAA0184 Disco-interacting protein 2, Drosophila, homolog of MOUSE: 10(Dip2) chr22_39096467_r_104 104 MKL1 NM_020831 INTRON OMIM: 604742 DCAMKL1 Doublecortin- and calmodulin kinase-like 1 chr2_144134265_r_104 104 ARHGAP15 NM_018460 INTRON chr2_205966442_y_104 104 ALS2CR19 NM_057177 INTRON chr2_205966442_y_104 104 ALS2CR19 NM_152526 INTRON chr2_74723370_y_104 104 DQX1 NM_133637 INTRON chr3_125478846_y_104 104 HAPIP NM_003947 INTRON chr3_137906872_y_104 104 NCK1 NM_006153 UTR chr3_174853676_y_104 104 NLGN1 NM_014932 INTRON OMIM: 600568 NLGN1 Neuroligin 1 chr4_103217425_y_104 104 BANK NM_017935 INTRON chr5_127783314_y_104 104 FBN2 NM_001999 INTRON OMIM: 121050 FBN2, CCA Fibrillin-2 Contractural arachnodactyly, congenital (3) MOUSE: 18(Fbn2) chr5_149606111_r_104 104 SLC6A7 NM_014228 INTRON OMIM: 606205 SLC6A7, PROT Solute carrier family 6 (neurotransmitter transporter, L-proline),member 7 MOUSE: 18(Slc6a7) chr5_43258752_y_104 104 MGC42105 NM_153361 UTR chr5_64710493_r_104 104 ADAMTS6 NM_014273 INTRON OMIM: 605008 ADAMTS6 A disintegrin-like and metalloproteinase with thrombospondin type 1motif, 6 chr6_111097830_r_104 104 CDK11 NM_015076 INTRON chr6_152491695_r_104 104 SYNE1 NM_033071 INTRON chr6_152491695_r_104 104 SYNE1 NM_133650 INTRON chr6_152491695_r_104 104 SYNE1 NM_015293 INTRON chr7_6173890_y_104 104 RAC1 NM_006908 INTRON OMIM: 607267 POLE3, CHARAC17, YBL Polymerase, DNA, epsilon-3 chr7_6173890_y_104 104 RAC1 NM_018890 INTRON OMIM: 607267 POLE3, CHARAC17, YBL Polymerase, DNA, epsilon-3 chr7_83378276_r_104 104 SEMA3A NM_006080 INTRON chr8_100387266_y_104 104 COH1 NM_017890 INTRON OMIM: 607817 COH1 COH1 gene Cohen syndrome, 216550 (3) chr8_100387266_y_104 104 COH1 NM_152564 INTRON OMIM: 607817 COH1 COH1 gene Cohen syndrome, 216550 (3) chr9_125312559_r_104 104 RALGPS1A NM_014636 INTRON chr9_126029976_r_104 104 ST6GALNAC6 NM_013443 INTRON chrX_109415798_r_104 104 DCX NM_000555 INTRON OMIM: 300121 DCX, DBCN, LISX Doublecortin Lissencephaly, X-linked, 300067 (3); Subcortical laminalheteropia, X-linked, 300 MOUSE: X(Dcx) chrX_109415798_r_104 104 DCX NM_178151 INTRON OMIM: 300121 DCX, DBCN, LISX Doublecortin Lissencephaly, X-linked, 300067 (3); Subcortical laminalheteropia, X-linked, 300 MOUSE: X(Dcx) chrX_109415798_r_104 104 DCX NM_178152 INTRON OMIM: 300121 DCX, DBCN, LISX Doublecortin Lissencephaly, X-linked, 300067 (3); Subcortical laminalheteropia, X-linked, 300 MOUSE: X(Dcx) chrX_109415798_r_104 104 DCX NM_178153 INTRON OMIM: 300121 DCX, DBCN, LISX Doublecortin Lissencephaly, X-linked, 300067 (3); Subcortical laminalheteropia, X-linked, 300 MOUSE: X(Dcx) chrX_14917679_y_104 104 BMX NM_001721 INTRON OMIM: 300101 BMX BMX non-receptor tyrosine kinase chrX_2246033_y_104 104 CD99 NM_002414 INTRON OMIM: 313470 CD99, MIC2, MIC2X CD99 antigen (MIC2 (monoclonal antibody 12E7)) distal to STS chrX_40501790_y_104 104 CASK NM_003688 INTRON OMIM: 300172 CASK Calcium/calmodulin-dependent serine protein kinase chrY_2246033_y_104 104 CD99 NM_002414 INTRON OMIM: 313470 CD99, MIC2, MIC2X CD99 antigen (MIC2 (monoclonal antibody 12E7)) distal to STS chr10_114541709_y_105 105 TCF7L2 NM_030756 INTRON OMIM: 602228 TCF7L2, TCF4 Transcription factor 7-like 2 chr10_16929016_r_105 105 CUBN NM_001081 INTRON OMIM: 602997 CUBN, IFCR, MGA1 Cubilin (intrinsic factor-cobalamin receptor) Megaloblastic anemia-1, Finnish type, 261100 (3) chr10_88223784_y_105 105 BMPR1A NM_004329 UTR OMIM: 601299 BMPR1A, ACVRLK3, ALK Bone morphogenetic protein receptor, type IA Polyposis, juvenile intestinal, 174900 (3); Cowden-like syndrome,158350 (3) chr11_19751223_y_105 105 NAV2 NM_145117 INTRON OMIM: 607026 NAV2, RAINB1, KIAA14 Neuron navigator 2 chr11_991313_y_105 105 AP2A2 NM_012305 INTRON chr12_5791604_r_105 105 C12orf3 NM_020373 INTRON chr12_5791857_r_105 105 C12orf3 NM_020373 INTRON chr12_80110150_y_105 105 FLJ21963 NM_024560 INTRON chr12_95243806_r_105 105 PCTK2 NM_002595 UTR chr13_75618588_r_105 105 PAM NM_015057 INTRON OMIM: 170270 PAM Peptidylglycine alpha-amidating monooxygenase MOUSE: 1(Pam) chr14_90375716_r_105 105 FBLN5 NM_006329 INTRON OMIM: 604580 FBLN5 Fibulin 5 Cutis laxa, autosomal recessive, 219100 (3); Cutis laxa, autosomaldominant, 1237 chr17_13688383_r_105 105 HS3ST3A1 NM_006042 INTRON OMIM: 604057 HS3ST3A1, 30ST3A1 Heparan sulfate D-glucosaminyl 3-0-sulfotransferase 3A1 MOUSE: 11(30st3a1) chr17_431766_r_105 105 FLJ10979 NM_018289 INTRON chr17_46776011_r_105 105 SCAP1 NM_003726 INTRON OMIM: 604969 SCAP1, SKAP55 SRC kinase-associated phosphoprotein 1, 55kD chr17_64206465_y_105 105 MGC33887 NM_145036 INTRON chr18_2990045_r_105 105 LPIN2 NM_014646 UTR OMIM: 605519 LPIN2 Lipin 2 MOUSE: 17(Lpin2) chr18_55043182_y_105 105 GRP NM_002091 INTRON OMIM: 608197 PGRPIA Peptidoglycan recognition protein, intermediate, alpha chr19_12514433_r_105 105 FLJ38281 NM_152601 UTR chr19_12514433_r_105 105 MGC26914 NM_144976 UTR chr19_53529461_y_105 105 FLJ10922 NM_018273 INTRON chr19_53537269_r_105 105 FLJ10922 NM_018273 INTRON chr1_151904798_y_105 105 KCNN3 NM_170782 INTRON OMIM: 602983 KCNN3, SK3, SKCA3 Potassium channel, calcium-activated, intermediate/small conductance,subfamily N chr1_151904798_y_105 105 KCNN3 NM_002249 INTRON OMIM: 602983 KCNN3, SK3, SKCA3 Potassium channel, calcium-activated, intermediate/small conductance,subfamily N chr1_199182022_r_105 105 LMOD1 NM_012134 INTRON chr1_199182022_r_105 105 ELF3 NM_004433 UTR OMIM: 602191 ELF3, ESX E74-like factor 3 (ETS domain transcription factor, serine box,epithelial-specif chr1_2125938_y_105 105 FLJ13941 NM_024848 INTRON chr20_53470755_y_105 105 CYP24A1 NM_000782 INTRON OMIM: 126065 CYP24A1, CYP24 Cytochrome P450, family 24, subfamily A, polypeptide 1(vitamin D 24-hydroxylase) MOUSE: 2(Cyp24) chr21_30003536_y_105 105 GRIK1 NM_175611 INTRON OMIM: 138245 GRIK1, GLUR5 Glutamate receptor, ionotropic, kainate 1 MOUSE: 16(Glur5) chr21_30003536_y_105 105 GRIK1 NM_000830 INTRON OMIM: 138245 GRIK1, GLUR5 Glutamate receptor, ionotropic, kainate 1 MOUSE: 16(Glur5) chr22_21797196_r_105 105 RTDR1 NM_014433 INTRON OMIM: 605663 RTDR1 Rhabdoid tumor deletion region protein 1 chr2_191731779_y_105 105 NAB1 NM_005966 INTRON OMIM: 600800 NAB1 NGFI-A-binding protein, ERG1-binding protein MOUSE: 1(Nab1) chr2_233742425_r_105 105 FLJ13612 NM_025202 INTRON chr2_234132809_y_105 105 INPP5D NM_005541 INTRON OMIM: 601582 INPP5D, SHIP Inositol polyphosphate-5-phosphatase, 145kD MOUSE: 1(Inpp5d) chr2_54403296_y_105 105 ACYP2 NM_138448 INTRON chr3_1317212_r_105 105 CNTN6 NM_014461 INTRON OMIM: 607220 CNTN6, NB3 Contactin 6 chr3_61615745_r_105 105 PTPRG NM_002841 INTRON OMIM: 176886 PTPRG, PTPG Protein tyrosine phosphatase, receptor type, gamma polypeptide chr3_85182847_y_105 105 LOC253559 NM_153184 INTRON chr4_20059603_y_105 105 SLIT2 NM_004787 INTRON OMIM: 603746 SLIT2 Slit, Drosophila, homolog of, 2 chr4_84058748_r_105 105 SCD4 NM_024906 INTRON OMIM: 608370 SCD4, ACOD4 Stearoyl-CoA desaturase 4 chr5_158377731_r_105 105 EBF NM_024007 INTRON OMIM: 164343 EBF, OLF1 Early B-cell factor (olfactory neuronal transcription factor 1) MOUSE: 11(Ebf) chr5_169433659_y_105 105 DOCK2 NM_004946 INTRON chr6_43670581_y_105 105 C6orf206 NM_152732 INTRON chr6_47680621_y_105 105 GPR111 NM_153839 INTRON chr6_6482794_r_105 105 FLJ33708 NM_173675 UTR chr7_102094911_r_105 105 MGC21636 NM_145032 INTRON chr7_99839223_y_105 105 TFR2 NM_003227 INTRON OMIM: 604720 TFR2, HFE3 Transferrin receptor 2 Hemochromatosis, type 3, 604250 (3) chr8_22404933_y_105 105 PPP3CC NM_005605 INTRON OMIM: 114107 PPP3CC, CALNA3 Protein phosphatase-3 (formerly 2B), catalytic subunit, gamma isoform(calcineuri chr8_3293259_r_105 105 CSMD1 NM_033225 INTRON OMIM: 608397 CSMD1, KIAA1890 Cub and Sushi multiple domains 1 chr8_40464584_y_105 105 FLJ13842 NM_024645 INTRON chr9_113370242_y_105 105 DEC1 NM_017418 UTR OMIM: 606393 ADAMDEC1, DECYSIN A disintegrin and metalloproteinase domain-like protein decysin 1 chr9_117388129_r_105 105 DBCCR1 NM_014618 INTRON OMIM: 602865 DBCCR1 Deleted in bladder cancer chromosome region candidate 1 chrX_10864072_r_105 105 ARHGAP6 NM_001174 UTR OMIM: 300118 ARHGAP6 Rho GTPase-activating protein-6 chrX_10864072_r_105 105 ARHGAP6 NM_013427 INTRON OMIM: 300118 ARHGAP6 Rho GTPase-activating protein-6 chrX_10864072_r_105 105 ARHGAP6 NM_006125 INTRON OMIM: 300118 ARHGAP6 Rho GTPase-activating protein-6 chrX_134515213_y_105 105 ARHGEF6 NM_004840 INTRON OMIM: 300267 ARHGEF6, MRX46, COOL Rho guanine nucleotide exchange factor-6 Mental retardation, X-linked nonspecific, type 46, 300436 (3) chrX_2351569_y_105 105 GYG2 NM_003918 INTRON OMIM: 300198 GYG2, GN2 Glycogenin 2 chrX_68480422_y_105 105 KIF4A NM_012310 INTRON chr10_100780907_r_106 106 CNNM1 NM_020348 INTRON OMIM: 607802 CNNM1, ACDP1 Cyclin M1 (ancient conserved domain protein 1) chr10_98675614_r_106 106 MGC14258 NM_032900 INTRON chr11_122513703_y_106 106 ASAM NM_024769 INTRON chr11_98840860_y_106 106 CNTN5 NM_014361 UTR OMIM: 607219 CNTN5, NB2 Contactin 5 chr11_98840860_y_106 106 CNTN5 NM_175566 UTR OMIM: 607219 CNTN5, NB2 Contactin 5 chr12_51853257_r_106 106 CSAD NM_015989 INTRON chr13_24103451_r_106 106 ATP8A2 NM_016529 INTRON OMIM: 605870 ATP8A2, ATPIB ATPase, class I, type 8A, member 2 chr14_33696252_y_106 106 KIAA0391 NM_014672 INTRON chr14_90247517_r_106 106 C14orf47 NM_152332 INTRON chr15_58390343_r_106 106 ANXA2 NM_004039 INTRON OMIM: 151740 ANXA2, ANX2L4, LPC2D Annexin A2 (lipocortin I) pseudogenes ANX2P1 on 4q21-q31; ANX2P2 on 9p13; ANX2P3 on 10q24-q22 chr15_64138811_r_106 106 MEGF11 NM_032445 UTR chr16_29892459_r_106 106 MVP NM_005115 INTRON OMIM: 605088 MVP, LRP Major vault protein, rat, homolog of chr16_29892459_r_106 106 MVP NM_017458 INTRON OMIM: 605088 MVP, LRP Major vault protein, rat, homolog of chr16_84225204_y_106 106 KIAA0703 NM_014861 INTRON chr17_4568187_y_106 106 MGC29671 NM_182538 INTRON chr17_46890062_y_106 106 SCAP1 NM_003726 INTRON OMIM: 604969 SCAP1, SKAP55 SRC kinase-associated phosphoprotein 1, 55kD chr17_5262427_r_106 106 USP6 NM_004505 UTR OMIM: 602748 DUSP6, MKP3, PYST1 Dual-specificity phosphatase-6 chr17_61212203_y_106 106 MRC2 NM_006039 INTRON chr17_75127294_y_106 106 CYGB NM_134268 INTRON chr18_59407570_y_106 106 SERPINB13 NM_012397 INTRON OMIM: 604445 SERPINB13, PI13, HUR Protease inhibitor 13 chr19_19121936_r_106 106 MEF2B NM_005919 INTRON OMIM: 600661 MEF2B MADS box transcription enhancer factor 2, polypeptide B (myocyteenhancer factor MOUSE: ?8(Mef2b) chr19_9970658_y_106 106 COL5A3 NM_015719 INTRON OMIM: 120216 COL5A3 Collagen, type V, alpha-3 polypeptide MOUSE: 9(Col5a3) chr1_18426923_r_106 106 PAX7 NM_002584 INTRON OMIM: 167410 PAX7 Paired box homeotic gene-7 fused with FKHR in rhabdomyosarcoma Rhabdomyosarcoma, alveolar, 268220 (3) MOUSE: 4(Pax7) chr1_18426923_r_106 106 PAX7 NM_013945 INTRON OMIM: 167410 PAX7 Paired box homeotic gene-7 fused with FKHR in rhabdomyosarcoma Rhabdomyosarcoma, alveolar, 268220 (3) MOUSE: 4(Pax7) chr1_2202177_y_106 106 RER1 NM_007033 INTRON chr1_47174081_y_106 106 UMP-CMPK NM_016308 INTRON chr20_52531712_r_106 106 FLJ33887 NM_173485 INTRON chr20_728710_r_106 106 C20orf55 NM_031424 UTR chr22_31534751_r_106 106 SYN3 NM_003490 INTRON OMIM: 602705 SYN3 Synapsin III ?relation to schizophrenia chr22_31534751_r_106 106 SYN3 NM_133632 INTRON OMIM: 602705 SYN3 Synapsin III ?relation to schizophrenia chr22_31534751_r_106 106 SYN3 NM_133633 INTRON OMIM: 602705 SYN3 Synapsin III ?relation to schizophrenia chr22_31534751_r_106 106 TIMP3 NM_000362 INTRON OMIM: 188826 TIMP3, SFD Tissue inhibitor of metalloproteinase-3 Sorsby fundus dystrophy, 136900 (3) chr2_170397387_r_106 106 LRP2 NM_004525 INTRON OMIM: 600073 LRP2 Low density lipoprotein-related protein 2 chr2_230215954_r_106 106 FLJ20701 NM_017933 INTRON chr3_157270165_y_106 106 KCNAB1 NM_172160 INTRON OMIM: 601141 KCNAB1, KCNA1B Potassium voltage-gated channel, shaker-related subfamily, beta member1 MOUSE: 3(Kcna1b) chr3_157270165_y_106 106 KCNAB1 NM_003471 INTRON OMIM: 601141 KCNAB1, KCNA1B Potassium voltage-gated channel, shaker-related subfamily, beta member1 MOUSE: 3(Kcna1b) chr3_180070626_y_106 106 WIG1 NM_022470 INTRON OMIM: 606452 WIG1 Wildtype p53-induced gene chr3_180070626_y_106 106 WIG1 NM_152240 INTRON OMIM: 606452 WIG1 Wildtype p53-induced gene chr3_188023400_y_106 106 SIAT1 NM_173216 UTR OMIM: 109675 SIAT1 Sialyltransferase-1 (beta-galactoside alpha-2,6-sialytransferase) chr3_188023400_y_106 106 SIAT1 NM_173217 UTR OMIM: 109675 SIAT1 Sialyltransferase-1 (beta-galactoside alpha-2,6-sialytransferase) chr3_190711314_r_106 106 TP73L NM_003722 INTRON OMIM: 603273 TP73L, TP63, KET, EE Tumor protein p63 (tumor protein p73-like) Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome3, 604292 (3); MOUSE: 16(Trp63) chr3_48786304_y_106 106 PRKAR2A NM_004157 INTRON OMIM: 176910 PRKAR2A Protein kinase, cAMP-dependent, regulatory, type II, alpha chr4_156086497_r_106 106 FGA NM_000508 INTRON OMIM: 134820 FGA Fibrinogen, alpha polypeptide Dysfibrinogenemia, alpha type, causing bleeding diathesis (3);Dysfibrinogenemia, chr4_156086497_r_106 106 FGA NM_021871 INTRON OMIM: 134820 FGA Fibrinogen, alpha polypeptide Dysfibrinogenemia, alpha type, causing bleeding diathesis (3);Dysfibrinogenemia, chr4_163478822_r_106 106 DKFZp566D234 NM_020116 INTRON chr4_62726738_y_106 106 LPHN3 NM_015236 INTRON chr4_79957848_r_106 106 ANXA3 NM_005139 INTRON OMIM: 106490 ANXA3, ANX3 Annexin A3 (lipocortin III) chr5_129070194_r_106 106 ADAMTS19 NM_133638 INTRON chr5_15730309_r_106 106 FBXL7 NM_012304 INTRON OMIM: 605656 FBXL7, FBL7 F-box and leucine-rich repeat protein 7 chr5_22104257_r_106 106 CDH12 NM_004061 INTRON OMIM: 600562 CDH12, CDHB Cadherin-12 (N-cadherin 2) pseudogene on 5q13 in SMA region chr6_129686951_r_106 106 LAMA2 NM_000426 INTRON OMIM: 156225 LAMA2, LAMM Laminin, alpha-2 (merosin) Muscular dystrophy, congenital merosin-deficient, 607855 (3);Muscular dystrophy, MOUSE: 10(dy, Lamm) chr6_34349540_r_106 106 NUDT3 NM_006703 INTRON chr6_41658117_r_106 106 MDFI NM_005586 INTRON OMIM: 604971 MDFI MYOD family inhibitor MOUSE: 17(Mdfi) chr7_116476972_r_106 106 WNT2 NM_003391 INTRON OMIM: 601968 WNT13, XWNT2 Wingless-type MMTV integration site family, member 13 chr7_87294890_r_106 106 ADAM22 NM_004194 INTRON OMIM: 603709 ADAM22 A disintegrin and metalloproteinase domain 22 chr7_87294890_r_106 106 ADAM22 NM_021721 INTRON OMIM: 603709 ADAM22 A disintegrin and metalloproteinase domain 22 chr7_87294890_r_106 106 ADAM22 NM_016351 INTRON OMIM: 603709 ADAM22 A disintegrin and metalloproteinase domain 22 chr7_87294890_r_106 106 ADAM22 NM_021722 INTRON OMIM: 603709 ADAM22 A disintegrin and metalloproteinase domain 22 chr7_87294890_r_106 106 ADAM22 NM_021723 INTRON OMIM: 603709 ADAM22 A disintegrin and metalloproteinase domain 22 chr8_110456681_r_106 106 PKHD1L1 NM_177531 INTRON chr8_119042429_r_106 106 EXT1 NM_000127 INTRON OMIM: 608177 EXT1 Exostosin 1 distal to TRPS1 Exostoses, multiple, type 1, 133700 (3); Chondrosarcoma, 215300 (3) MOUSE: 15(Ext1) chr9_34209797_y_106 106 UBAP1 NM_016525 UTR chrX_28538426_y_106 106 IL1RAPL1 NM_014271 INTRON chr10_101220042_r_107 107 ABCC2 NM_000392 INTRON OMIM: 601107 ABCC2, CMOAT ATP-binding cassette, subfamily C, member 2(canalicular multispecific organic an Dubin-Johnson syndrome, 237500 (3) MOUSE: 19(Cmoat) chr10_120945668_r_107 107 RGS10 NM_002925 INTRON chr10_26738030_r_107 107 APBB1IP NM_019043 UTR chr10_29802210_r_107 107 SVIL NM_021738 INTRON OMIM: 604126 SVIL Supervillin chr10_29802210_r_107 107 SVIL NM_003174 INTRON OMIM: 604126 SVIL Supervillin chr11_44894592_r_107 107 LOC90139 NM_130783 INTRON chr12_49273883_y_107 107 FLJ34278 NM_173602 INTRON chr12_62271988_r_107 107 FLJ32949 NM_173812 INTRON chr12_70262987_r_107 107 GPR49 NM_003667 INTRON chr14_75249792_r_107 107 KIAA0759 NM_015305 INTRON chr16_20987758_r_107 107 DKFZp434N074 NM_017539 INTRON chr17_38012850_y_107 107 CRK7 NM_016507 INTRON chr17_45726995_r_107 107 CDC27 NM_001256 INTRON OMIM: 116946 CDC27 Cell division cycle 27 between ERBB2 and PRKCA MOUSE: 11(Cdc27) chr17_58885408_r_107 107 USP32 NM_032582 INTRON OMIM: 607740 USP32, USP10 Ubiquitin-specific protease 32 chr17_72351220_y_107 107 FLJ40319 NM_182564 INTRON chr18_59097869_r_107 107 BCL2 NM_000633 INTRON OMIM: 603827 BCL2L11, BIM BCL2-like 11 ?2p13 chr19_2590816_r_107 107 FLJ00058 NM_052847 UTR chr19_35687113_y_107 107 KIAA0390 NM_014717 INTRON chr19_6722778_r_107 107 TRIP10 NM_004240 UTR chr19_798491_r_107 107 POLRMT NM_005035 UTR OMIM: 601778 POLRMT, APOLMT Polymerase (RNA) mitochondrial (DNA directed) chr19_798491_r_107 107 PRTN3 NM_002777 INTRON OMIM: 177020 PRTN3, AGP7 Proteinase-3 (serine proteinase, neutrophil, Wegener granulomatosisautoantigen) MOUSE: 10(Prtn3) chr1_11843030_y_107 107 TNFRSF8 NM_001243 INTRON OMIM: 153243 TNFRSF8, CD30, D1S16 Tumor necrosis factor receptor superfamily, member 8(CD30 antigen; Ki-1 antigen) MOUSE: 4(Cd30) chr1_195900270_y_107 107 PTPRC NM_080923 INTRON OMIM: 151460 PTPRC, CD45, LCA Protein tyrosine phosphatase, receptor type, c polypeptide {Multiple sclerosis, susceptibility to}, 126200 (3); Severecombined immunodefici MOUSE: 1(Ly5) chr1_195900270_y_107 107 PTPRC NM_002838 INTRON OMIM: 151460 PTPRC, CD45, LCA Protein tyrosine phosphatase, receptor type, c polypeptide {Multiple sclerosis, susceptibility to}, 126200 (3); Severecombined immunodefici MOUSE: 1(Ly5) chr1_195900270_y_107 107 PTPRC NM_080921 INTRON OMIM: 151460 PTPRC, CD45, LCA Protein tyrosine phosphatase, receptor type, c polypeptide {Multiple sclerosis, susceptibility to}, 126200 (3); Severecombined immunodefici MOUSE: 1(Ly5) chr1_195900270_y_107 107 PTPRC NM_080922 INTRON OMIM: 151460 PTPRC, CD45, LCA Protein tyrosine phosphatase, receptor type, c polypeptide {Multiple sclerosis, susceptibility to}, 126200 (3); Severecombined immunodefici MOUSE: 1(Ly5) chr1_201839604_r_107 107 MDM4 NM_002393 UTR OMIM: 602704 MDM4 Mouse double minute 4, homolog of MOUSE: 1(Mdm4) chr1_238343605_y_107 107 RGS7 NM_002924 INTRON chr1_49954588_r_107 107 ELAVL4 NM_021952 INTRON OMIM: 168360 ELAVL4, HUD, PNEM Embryonic lethal, abnormal vision, Drosophila, homolog of, like-4(Hu antigen D) Neuropathy, paraneoplastic sensory (1) MOUSE: 4(Hud) chr1_8374175_r_107 107 RERE NM_012102 INTRON OMIM: 605226 RERE RE repeats-encoding gene chr20_246618_r_107 107 C20orf96 NM_153269 UTR chr20_52289406_y_107 107 FLJ33887 NM_173485 INTRON chr21_33088664_y_107 107 C21orf62 NM_019596 UTR chr21_41078569_r_107 107 DSCAM NM_001389 INTRON OMIM: 602523 DSCAM Down syndrome cell adhesion molecule chr22_32066753_y_107 107 LARGE NM_004737 INTRON OMIM: 603590 LARGE Acetylglucosaminyltransferase-like protein ?Meningioma (2) chr22_32066753_y_107 107 LARGE NM_133642 INTRON OMIM: 603590 LARGE Acetylglucosaminyltransferase-like protein ?Meningioma (2) chr22_40647165_y_107 107 MGC26816 NM_152613 INTRON chr22_41779994_y_107 107 BZRP NM_007311 UTR OMIM: 109610 BZRP Benzodiazepine receptor, peripheral type (benzodiazepine peripheralbinding site) MOUSE: 15(Bzrp) chr22_41779994_y_107 107 BZRP NM_000714 UTR OMIM: 109610 BZRP Benzodiazepine receptor, peripheral type (benzodiazepine peripheralbinding site) MOUSE: 15(Bzrp) chr2_213070367_r_107 107 ERBB4 NM_005235 INTRON OMIM: 600543 ERBB4, HER4 Avian erythroblastic leukemia viral (v-erb-b2) oncogene homolog 4 chr3_117440137_y_107 107 LSAMP NM_002338 INTRON OMIM: 603241 LSAMP, LAMP Limbic system-associated membrane protein MOUSE: 16(Lsamp) chr3_125903718_r_107 107 ITGB5 NM_002213 INTRON chr3_197385793_r_107 107 LOC116211 NM_138461 UTR chr4_141296775_r_107 107 MAML3 NM_018717 INTRON chr4_15774582_r_107 107 PROM1 NM_006017 INTRON OMIM: 604365 PROM1, PROML1, AC133 Prominin 1 Retinal degeneration, autosomal recessive, prominin-related (3) chr4_20978786_r_107 107 KCNIP4 NM_147183 INTRON OMIM: 608182 KCNIP4, KCHIP4 Kv channel-interacting protein 4 chr4_20978786_r_107 107 KCNIP4 NM_147182 UTR OMIM: 608182 KCNIP4, KCHIP4 Kv channel-interacting protein 4 chr4_2200802_r_107 107 MGC4701 NM_024511 INTRON chr4_46180466_r_107 107 GABRA2 NM_000807 INTRON OMIM: 137140 GABRA2 Gamma-aminobutyric acid (GABA) A receptor, alpha-2 MOUSE: 5(Gabra2) chr4_47092540_y_107 107 GABRB1 NM_000812 INTRON OMIM: 137190 GABRB1 Gamma-aminobutyric acid (GABA) A receptor, beta-1 MOUSE: 5(Gabrb1) chr4_47092540_y_107 107 COX7B2 NM_130902 UTR chr4_5166954_y_107 107 HSA250839 NM_018401 INTRON chr4_6402967_y_107 107 PPP2R2C NM_181876 INTRON OMIM: 605997 PPP2R2C, PR52 Protein phosphatase 2A, regulatory subunit B, gamma isoform chr4_6402967_y_107 107 PPP2R2C NM_020416 INTRON OMIM: 605997 PPP2R2C, PR52 Protein phosphatase 2A, regulatory subunit B, gamma isoform chr5_102673548_y_107 107 LOC90355 NM_033211 UTR chr5_156465267_r_107 107 HAVCR1 NM_012206 INTRON OMIM: 606518 HAVCR1, HAVCR Hepatitis A virus cellular receptor 1 chr5_167808720_r_107 107 KIBRA NM_015238 INTRON chr5_90214751_y_107 107 MASS1 NM_032119 INTRON OMIM: 602851 MASS1, VLGR1, KIAA06 Monogenic, audiogenic seizure susceptibility 1, mouse, homolog of(very large G p Convulsions, familial febrile, 4, 604352 (3) MOUSE: 13(Frings, mass1) chr6_32106320_r_107 107 TNXB NM_019105 INTRON OMIM: 600985 TNXB, TNX, TNXB1, TN Tenascin X Ehlers-Danlos due to tenascin X deficiency, 606408 (3);Ehlers-Danlos syndrome, h chr6_32117303_r_107 107 TNXB NM_019105 INTRON OMIM: 600985 TNXB, TNX, TNXB1, TN Tenascin X Ehlers-Danlos due to tenascin X deficiency, 606408 (3);Ehlers-Danlos syndrome, h chr7_104434042_r_107 107 SRPK2 NM_003138 INTRON chr7_104434042_r_107 107 SRPK2 NM_182691 INTRON chr7_104434042_r_107 107 SRPK2 NM_182692 INTRON chr7_146851557_r_107 107 CNTNAP2 NM_014141 INTRON OMIM: 604569 CNTNAP2, CASPR2, NRX Contactin-associated protein-like 2 chr7_64797446_r_107 107 LOC154807 NM_173517 UTR chr7_70849033_r_107 107 CALN1 NM_031468 INTRON chr8_113463295_y_107 107 CSMD3 NM_052900 INTRON OMIM: 608399 CSMD3, KIAA1894 Cub and Sushi multiple domains 3 chr8_118782839_r_107 107 EXT1 NM_000127 INTRON OMIM: 608177 EXT1 Exostosin 1 distal to TRPS1 Exostoses, multiple, type 1, 133700 (3); Chondrosarcoma, 215300 (3) MOUSE: 15(Ext1) chr8_13133532_y_107 107 DLC1 NM_182643 INTRON OMIM: 604050 DLEC1, DLC1 Deleted in lung and esophageal cancer 1 Lung cancer, 211980 (1); Esophageal cancer, 133239 (1) chr8_13133532_y_107 107 DLC1 NM_024767 INTRON OMIM: 604050 DLEC1, DLC1 Deleted in lung and esophageal cancer 1 Lung cancer, 211980 (1); Esophageal cancer, 133239 (1) chr8_27798253_r_107 107 MGC45780 NM_173833 INTRON chr8_40464820_y_107 107 FLJ13842 NM_024645 INTRON chr8_69551785_r_107 107 VEST1 NM_052958 INTRON chr9_109890858_y_107 107 FLJ32779 NM_173521 INTRON chr9_134354203_r_107 107 MGC23427 NM_144653 INTRON chr9_136037366_y_107 107 CACNA1B NM_000718 INTRON OMIM: 601012 CACNA1B, CACNL1A5 Calcium channel, voltage-dependent, L type, alpha 1B subunit chr9_36963081_r_107 107 PAX5 NM_016734 INTRON OMIM: 167414 PAX5, BSAP Paired box homeotic gene-5 (B-cell lineage specific activatorprotein) Lymphoplasmacytoid lymphoma (1) MOUSE: 4(Pax5) chrX_66294605_y_107 107 OPHN1 NM_002547 INTRON OMIM: 300127 OPHN1 Oligophrenin-1 Mental retardation, X-linked, 60 (3) chr11_19183191_y_108 108 CSRP3 NM_003476 UTR OMIM: 600824 CSRP3, CRP3, CLP, CM Cysteine- and glycine-rich protein 3 Cardiomyopathy, dilated, 1M, 607482 (3) chr12_116172209_y_108 108 NOS1 NM_000620 INTRON OMIM: 163731 NOS1 Nitric oxide synthase 1, neuronal MOUSE: 5(Nos1) chr12_85651786_y_108 108 HGNT-IV-H NM_013244 UTR chr12_99877667_r_108 108 FLJ34221 NM_178826 INTRON chr13_71284100_r_108 108 PIBF1 NM_006346 INTRON OMIM: 607532 PIBF1 Progesterone-induced blocking factor 1 chr14_75954113_r_108 108 LOC145501 NM_182509 INTRON chr15_39473338_y_108 108 KIAA0252 NM_015138 INTRON chr15_67092829_y_108 108 FLJ33768 NM_173610 UTR chr16_78539329_y_108 108 WWOX NM_018560 UTR OMIM: 605131 WWOX, FOR WW domain-containing oxidoreductase Esophageal squamous cell carcinoma, 133239 (3) MOUSE: 8(Wox1, Fra8E1) chr16_78539329_y_108 108 WWOX NM_016373 INTRON OMIM: 605131 WWOX, FOR WW domain-containing oxidoreductase Esophageal squamous cell carcinoma, 133239 (3) MOUSE: 8(Wox1, Fra8E1) chr16_78539329_y_108 108 WWOX NM_130788 INTRON OMIM: 605131 WWOX, FOR WW domain-containing oxidoreductase Esophageal squamous cell carcinoma, 133239 (3) MOUSE: 8(Wox1, Fra8E1) chr16_78539329_y_108 108 WWOX NM_130790 INTRON OMIM: 605131 WWOX, FOR WW domain-containing oxidoreductase Esophageal squamous cell carcinoma, 133239 (3) MOUSE: 8(Wox1, Fra8E1) chr16_78539329_y_108 108 WWOX NM_130792 INTRON OMIM: 605131 WWOX, FOR WW domain-containing oxidoreductase Esophageal squamous cell carcinoma, 133239 (3) MOUSE: 8(Wox1, Fra8E1) chr1_114519106_y_108 108 AMPD1 NM_000036 INTRON OMIM: 102770 AMPD1 Adenosine monophosphate deaminase-1, muscle Myoadenylate deaminase deficiency (3) MOUSE: 3(Ampd1) chr1_181669136_y_108 108 C1orf21 NM_030806 UTR chr20_3518209_y_108 108 ATRN NM_012070 INTRON OMIM: 603130 ATRN, MGCA Attractin (mahogany, mouse, homolog of) MOUSE: 2(Atrn) chr20_3518209_y_108 108 ATRN NM_139322 INTRON OMIM: 603130 ATRN, MGCA Attractin (mahogany, mouse, homolog of) MOUSE: 2(Atrn) chr20_3518209_y_108 108 ATRN NM_139321 INTRON OMIM: 603130 ATRN, MGCA Attractin (mahogany, mouse, homolog of) MOUSE: 2(Atrn) chr20_4206658_y_108 108 ADRA1D NM_000678 INTRON OMIM: 104219 ADRA1D, ADRA1A Adrenergic, alpha-1D-, receptor incorrectly assigned to 5q MOUSE: 11(Adra1a) chr21_25995554_y_108 108 JAM2 NM_021219 INTRON OMIM: 606870 JAM2, VEJAM Junctional adhesion molecule 2 chr21_32216175_r_108 108 HUNK NM_014586 INTRON OMIM: 606532 HUNK Hormonally upregulated NEU-associated kinase MOUSE: 16(Hunk) chr3_116680634_y_108 108 GAP43 NM_002045 INTRON OMIM: 162060 GAP43 Neuron growth-associated protein 43 MOUSE: 16(Gap43) chr3_170230399_r_108 108 MDS1 NM_004991 INTRON OMIM: 600049 MDS1 Myelodysplasia syndrome-1 cen--EVI1--MDS1--EAP--tel Myelodysplasia syndrome-1 (3) chr3_49983146_y_108 108 RBM6 NM_005777 INTRON OMIM: 606886 RBM6, DEF3 RNA-binding motif protein 6 MOUSE: 9(Rbm6) chr3_53512222_y_108 108 CACNA1D NM_000720 INTRON OMIM: 114206 CACNA1D, CACNL1A2, C Calcium channel, voltage-dependent, L type, alpha 1D subunit MOUSE: 14(Cch1a2) chr3_61938695_y_108 108 PTPRG NM_002841 INTRON OMIM: 176886 PTPRG, PTPG Protein tyrosine phosphatase, receptor type, gamma polypeptide chr3_79086301_y_108 108 ROBO1 NM_002941 INTRON OMIM: 602430 ROBO1, DUTT1, SAX3 Roudnabout, Drosophila, homolog of, 1 chr4_147990419_r_108 108 DKFZP566M114 NM_032128 INTRON chr4_169914339_r_108 108 FLJ20035 NM_017631 INTRON chr4_89818891_r_108 108 FLJ20637 NM_017912 INTRON chr6_129903180_r_108 108 ARHGAP18 NM_033515 INTRON chr6_16670628_r_108 108 SCA1 NM_000332 UTR OMIM: 607346 SCA19 Spinocerebellar ataxia 19 close to marker D1S534 Spinocerebellar ataxia 19 (2) chr6_38058115_y_108 108 TEX27 NM_021943 INTRON chr7_100693053_y_108 108 COL26A1 NM_133457 INTRON chr7_71971268_y_108 108 FKBP6 NM_003602 INTRON OMIM: 604839 FKBP6 FK506-binding protein 6 chr8_134520345_r_108 108 SIAT4A NM_003033 UTR chr8_134520345_r_108 108 SIAT4A NM_173344 UTR chr8_141053672_r_108 108 MGC4737 NM_031466 UTR chr8_76416221_y_108 108 HNF4G NM_004133 UTR OMIM: 605966 HNF4G Hepatocyte nuclear factor 4-gamma MOUSE: 3(Hnf4g) chr8_97219427_r_108 108 CGI-12 NM_015942 INTRON chr9_113282652_y_108 108 DEC1 NM_017418 UTR OMIM: 606393 ADAMDEC1, DECYSIN A disintegrin and metalloproteinase domain-like protein decysin 1 chr9_67067189_r_108 108 PIP5K1B NM_003558 INTRON OMIM: 602745 PIP5K1B, STM7, MSS4 Phosphatidylinositol-4-phosphate 5-kinase, type I, beta chrX_107427470_r_108 108 GUCY2F NM_001522 INTRON OMIM: 300041 GUCY2F, GUC2F Guanylate cyclase 2F MOUSE: X(Gucy2f) chrX_118331936_r_108 108 LAMP2 NM_002294 INTRON OMIM: 309060 LAMP2, LAMPB Lysosome-associated membrane protein-2 Glycogen storage disease IIb, 300257 (3) MOUSE: X(Lamp2) chrX_118331936_r_108 108 LAMP2 NM_013995 INTRON OMIM: 309060 LAMP2, LAMPB Lysosome-associated membrane protein-2 Glycogen storage disease IIb, 300257 (3) MOUSE: X(Lamp2) chrX_127666820_r_108 108 ZDHHC9 NM_016032 INTRON chrX_70702329_r_108 108 PHKA1 NM_002637 INTRON OMIM: 311870 PHKA1 Phosphorylase kinase, muscle, alpha polypeptide ?proximal and close to PGKA; Muscle glycogenosis (3) MOUSE: X(Phka) chr10_22080263_r_109 109 DNAJC1 NM_022365 INTRON chr10_23624395_r_109 109 MGC46732 NM_153714 INTRON chr10_35724284_y_109 109 CFP1 NM_181698 UTR chr10_35724284_y_109 109 CFP1 NM_145012 INTRON chr10_52939042_r_109 109 PRKG1 NM_006258 INTRON OMIM: 176894 PRKG1, PRKG1B, PRKGR Protein kinase, cGMP-dependent, regulatory, type I chr10_72605120_y_109 109 CDH23 NM_052836 INTRON OMIM: 605516 CDH23, USH1D Cadherin-23 (otocadherin) between D10S529 and D10S573 Usher syndrome, type 1D, 601067 (3); Deafness, autosomal recessive12, 601386 (3) MOUSE: 10(Cdh23, v) chr10_72605120_y_109 109 CDH23 NM_022124 INTRON OMIM: 605516 CDH23, USH1D Cadherin-23 (otocadherin) between D10S529 and D10S573 Usher syndrome, type 1D, 601067 (3); Deafness, autosomal recessive12, 601386 (3) MOUSE: 10(Cdh23, v) chr10_78491889_y_109 109 KCNMA1 NM_002247 INTRON OMIM: 600150 KCNMA1, SLO Potassium large conductance calcium-activated channel, subfamily M,alpha member chr11_113342757_r_109 109 HTR3B NM_006028 INTRON OMIM: 604654 HTR3B 5-hydroxytryptamine receptor 3B chr11_83311587_r_109 109 DLG2 NM_001364 INTRON OMIM: 603583 DLG2 Discs large, Drosophila, homolog of, 2(channel-associated protein of synapses, 1 chr13_69917635_r_109 109 DACH NM_004392 INTRON OMIM: 603803 DACH Dachshund, Drosophila, homolog of MOUSE: 13(Dach) chr13_69917635_r_109 109 DACH NM_080759 INTRON OMIM: 603803 DACH Dachshund, Drosophila, homolog of MOUSE: 13(Dach) chr13_69917635_r_109 109 DACH NM_080760 INTRON OMIM: 603803 DACH Dachshund, Drosophila, homolog of MOUSE: 13(Dach) chr13_97080451_r_109 109 SLC15A1 NM_005073 INTRON OMIM: 600544 SLC15A1, HPECT1 Solute carrier family 15 (oligopeptide transporter), member 1 chr14_62316643_y_109 109 SYNE2 NM_015180 UTR chr14_92945566_r_109 109 SERPINA3 NM_001085 UTR OMIM: 107280 SERPINA3, AACT, ACT Alpha-1-antichymotrypsin 220kb from PI Alpha-1-antichymotrypsin deficiency (3); Cerebrovasculardisease, occlusive (3) chr14_92945566_r_109 109 OL-64 NM_173850 INTRON chr15_67308715_y_109 109 MPRG NM_017705 UTR OMIM: 607781 MPRG Membrane progestin receptor, gamma chr15_83172891_r_109 109 SLC28A1 NM_004213 INTRON OMIM: 606207 SLC28A1, CNT1 Solute carrier family 28 (sodium-coupled nucleoside transporter),member 1 chr16_78039904_y_109 109 WWOX NM_130791 INTRON OMIM: 605131 WWOX, FOR WW domain-containing oxidoreductase Esophageal squamous cell carcinoma, 133239 (3) MOUSE: 8(Wox1, Fra8E1) chr16_78039904_y_109 109 WWOX NM_018560 INTRON OMIM: 605131 WWOX, FOR WW domain-containing oxidoreductase Esophageal squamous cell carcinoma, 133239 (3) MOUSE: 8(Wox1, Fra8E1) chr16_78039904_y_109 109 WWOX NM_016373 INTRON OMIM: 605131 WWOX, FOR WW domain-containing oxidoreductase Esophageal squamous cell carcinoma, 133239 (3) MOUSE: 8(Wox1, Fra8E1) chr16_78039904_y_109 109 WWOX NM_130788 INTRON OMIM: 605131 WWOX, FOR WW domain-containing oxidoreductase Esophageal squamous cell carcinoma, 133239 (3) MOUSE: 8(Wox1, Fra8E1) chr16_78039904_y_109 109 WWOX NM_130790 INTRON OMIM: 605131 WWOX, FOR WW domain-containing oxidoreductase Esophageal squamous cell carcinoma, 133239 (3) MOUSE: 8(Wox1, Fra8E1) chr16_78039904_y_109 109 WWOX NM_130792 INTRON OMIM: 605131 WWOX, FOR WW domain-containing oxidoreductase Esophageal squamous cell carcinoma, 133239 (3) MOUSE: 8(Wox1, Fra8E1) chr17_125928_r_109 109 RPH3AL NM_006987 INTRON OMIM: 604881 RPH3AL, NOC2 Rabphilin 3A-like chr17_29398082_y_109 109 CENTA2 NM_018404 INTRON chr17_31864715_y_109 109 ACCN1 NM_001094 INTRON OMIM: 601784 ACCN1, BNC1, MDEG Amiloride-sensitive cation channel 1, neuronal (degenerin) chr17_35534460_y_109 109 AATF NM_012138 INTRON chr17_72351084_y_109 109 FLJ40319 NM_182564 INTRON chr17_9827376_y_109 109 FLJ30626 NM_153210 UTR chr18_8230752_r_109 109 PTPRM NM_002845 INTRON OMIM: 176888 PTPRM, PTPRL1, RPTPM Protein tyrosine phosphatase, receptor type, mu polypeptide chr19_54389621_y_109 109 TRPM4 NM_017636 INTRON OMIM: 606936 TRPM4 Transient receptor potential cation channel, subfamily M, member 4 chr19_59611889_r_109 109 ILT7 NM_012276 INTRON chr1_61632247_y_109 109 INADL NM_005799 INTRON chr1_61632247_y_109 109 INADL NM_176877 INTRON chr1_61632247_y_109 109 INADL NM_176878 INTRON chr1_61632247_y_109 109 INADL NM_170605 INTRON chr1_9567703_r_109 109 CLSTN1 NM_014944 INTRON chr20_249518_r_109 109 C20orf96 NM_153269 INTRON chr2_119845382_y_109 109 MARCO NM_006770 INTRON chr2_125508642_r_109 109 caspr5 NM_130773 INTRON chr2_125508642_r_109 109 caspr5 NM_138996 INTRON chr2_191756018_y_109 109 NAB1 NM_005966 INTRON OMIM: 600800 NAB1 NGFI-A-binding protein, ERG1-binding protein MOUSE: 1(Nab1) chr2_44875102_r_109 109 FLJ23451 NM_024766 INTRON chr2_50648181_y_109 109 NRXN1 NM_004801 INTRON OMIM: 600565 NRXN1 Neurexin 1 chr3_79520193_r_109 109 ROBO1 NM_002941 INTRON OMIM: 602430 ROBO1, DUTT1, SAX3 Roudnabout, Drosophila, homolog of, 1 chr4_111136848_r_109 109 RRH NM_006583 UTR OMIM: 605224 RRH Rhodopsin homolog, retinal pigment epithelium-derived (peropsin) MOUSE: 3(Rrh) chr4_111136848_r_109 109 IF NM_000204 INTRON OMIM: 603320 MMP23A, MMP21, MIFR Matrix metalloproteinase 23A chr4_169882841_r_109 109 FLJ20035 NM_017631 INTRON chr4_94547747_r_109 109 GRID2 NM_001510 INTRON OMIM: 602368 GRID2 Glutamate receptor, ionotropic, delta-2 MOUSE: 6(Grid2) chr4_94912777_y_109 109 GRID2 NM_001510 INTRON OMIM: 602368 GRID2 Glutamate receptor, ionotropic, delta-2 MOUSE: 6(Grid2) chr5_176504779_y_109 109 FGFR4 NM_002011 INTRON OMIM: 134935 FGFR4 Fibroblast growth factor receptor-4 distal to DRD1 {Cancer progression/metastasis} (3) MOUSE: 13(Fgfr4) chr5_176504779_y_109 109 FGFR4 NM_022963 INTRON OMIM: 134935 FGFR4 Fibroblast growth factor receptor-4 distal to DRD1 {Cancer progression/metastasis} (3) MOUSE: 13(Fgfr4) chr5_54784404_r_109 109 PPAP2A NM_003711 INTRON chr5_54784404_r_109 109 PPAP2A NM_176895 INTRON chr5_54824182_r_109 109 PPAP2A NM_003711 INTRON chr5_54824182_r_109 109 PPAP2A NM_176895 INTRON chr6_56088486_r_109 109 COL21A1 NM_030820 INTRON chr7_153626522_r_109 109 DPP6 NM_130797 INTRON OMIM: 126141 DPP6 Dipeptidylpeptidase VI MOUSE: 5(Dppx, Dpp6) chr7_153626522_r_109 109 DPP6 NM_001936 INTRON OMIM: 126141 DPP6 Dipeptidylpeptidase VI MOUSE: 5(Dppx, Dpp6) chr7_64773128_y_109 109 LOC154807 NM_173517 UTR chr7_72661546_y_109 109 WBSCR27 NM_152559 INTRON chr7_99978474_y_109 109 ZAN NM_003386 INTRON OMIM: 602372 ZAN Zonadhesin MOUSE: 5(Zan) chr7_99978474_y_109 109 ZAN NM_173055 INTRON OMIM: 602372 ZAN Zonadhesin MOUSE: 5(Zan) chr7_99978474_y_109 109 ZAN NM_173056 INTRON OMIM: 602372 ZAN Zonadhesin MOUSE: 5(Zan) chr7_99978474_y_109 109 ZAN NM_173057 INTRON OMIM: 602372 ZAN Zonadhesin MOUSE: 5(Zan) chr7_99978474_y_109 109 ZAN NM_173058 INTRON OMIM: 602372 ZAN Zonadhesin MOUSE: 5(Zan) chr7_99978474_y_109 109 ZAN NM_173059 INTRON OMIM: 602372 ZAN Zonadhesin MOUSE: 5(Zan) chr8_106503212_y_109 109 ZFPM2 NM_012082 INTRON OMIM: 603693 ZFPM2, FOG2 Zinc finger protein, multitype 2 (friend of GATA2) chr9_17612985_y_109 109 SH3GL2 NM_003026 INTRON OMIM: 604465 SH3GL2, SH3P4 SH3 domain, GRB2-like, 2 chrX_18006206_y_109 109 CDKL5 NM_003159 INTRON OMIM: 300203 CDKL5, STK9 Cyclin-dependent kinase-like 5(serine/threonine protein kinase 9) MOUSE: X(Stk9) chrX_28425442_y_109 109 IL1RAPL1 NM_014271 INTRON chr10_115937173_r_110 110 ABLIM1 NM_006720 UTR chr10_115937173_r_110 110 ABLIM1 NM_006719 INTRON chr10_115937173_r_110 110 ABLIM1 NM_002313 INTRON chr10_118754044_r_110 110 LOC118987 NM_173791 INTRON chr10_15182225_r_110 110 NMT2 NM_004808 INTRON OMIM: 602478 DNMT2 DNA methyltransferase-2 chr10_78073597_r_110 110 KCNMA1 NM_002247 INTRON OMIM: 600150 KCNMA1, SLO Potassium large conductance calcium-activated channel, subfamily M,alpha member chr10_94761183_r_110 110 FER1L3 NM_013451 INTRON chr10_94761183_r_110 110 FER1L3 NM_133337 INTRON chr11_83171685_y_110 110 DLG2 NM_001364 INTRON OMIM: 603583 DLG2 Discs large, Drosophila, homolog of, 2(channel-associated protein of synapses, 1 chr13_97053419_r_110 110 SLC15A1 NM_005073 INTRON OMIM: 600544 SLC15A1, HPECT1 Solute carrier family 15 (oligopeptide transporter), member 1 chr14_77814944_r_110 110 NRXN3 NM_004796 INTRON OMIM: 600567 NRXN3 Neurexin 3 chr14_77814944_r_110 110 NRXN3 NM_138970 INTRON OMIM: 600567 NRXN3 Neurexin 3 chr14_89500725_r_110 110 RPS6KA5 NM_004755 INTRON OMIM: 603607 RPS6KA5, MSK1 Ribosomal protein S6 kinase, 90kD, 5 chr14_89500725_r_110 110 RPS6KA5 NM_182398 INTRON OMIM: 603607 RPS6KA5, MSK1 Ribosomal protein S6 kinase, 90kD, 5 chr16_12800317_r_110 110 FLJ11151 NM_018340 INTRON chr16_24072668_r_110 110 PRKCB1 NM_002738 INTRON OMIM: 176970 PRKCB1, PKCB Protein kinase C, beta 1 polypeptide chr16_56375864_r_110 110 MT4 NM_032935 INTRON OMIM: 606598 GDAP1, CMT4A, CMT2K, Ganglioside-induced differentiation-associated protein 1 Charcot-Marie-Tooth disease, type 4A, 214400 (3);Charcot-Marie-Tooth disease, ty chr16_83136440_y_110 110 CDH13 NM_001257 INTRON OMIM: 601364 CDH13, CDHH Cadherin-13 (H-cadherin, heart) chr17_10053625_y_110 110 GAS7 NM_005890 INTRON OMIM: 603127 GAS7 Growth arrest-specific 7 MOUSE: 11(gas7) chr17_10053625_y_110 110 GAS7 NM_003644 INTRON OMIM: 603127 GAS7 Growth arrest-specific 7 MOUSE: 11(gas7) chr18_33330225_y_110 110 BRUNOL4 NM_020180 INTRON chr18_604287_r_110 110 CLUL1 NM_014410 UTR chr19_59014883_r_110 110 NALP12 NM_144687 INTRON chr19_6104871_r_110 110 BGR NM_030924 INTRON OMIM: 300190 SH3BGR SH3-binding domain glutamic acid-rich protein-like chr1_152485688_y_110 110 PKLR NM_181871 INTRON OMIM: 266200 PKLR, PK1 Pyruvate kinase, liver and RBC type Anemia, hemolytic, due to PK deficiency (3) MOUSE: 3(Pk1) chr1_152485688_y_110 110 PKLR NM_000298 INTRON OMIM: 266200 PKLR, PK1 Pyruvate kinase, liver and RBC type Anemia, hemolytic, due to PK deficiency (3) MOUSE: 3(Pk1) chr1_182070025_r_110 110 C1orf24 NM_052966 INTRON chr1_182070025_r_110 110 C1orf24 NM_022083 UTR chr1_244100135_r_110 110 SBZF3 NM_020394 INTRON chr1_94138790_y_110 110 PARG1 NM_004815 INTRON OMIM: 601487 PPARG, PPARG1, PPARG Peroxisome proliferator activated receptor, gamma PPARG1, PPARG2 from same gene Obesity, severe, 601665 (3); [Obesity, resistance to] (3);Diabetes mellitus, ins chr20_5914492_y_110 110 CGI-09 NM_015939 INTRON chr21_36430152_r_110 110 CBR3 NM_001236 INTRON OMIM: 603608 CBR3 Carbonyl reductase 3 chr21_38500166_y_110 110 DSCR10 NM_148676 UTR chr22_29887098_y_110 110 FLJ38628 NM_152267 UTR chr22_43596469_r_110 110 LOC112885 NM_138415 INTRON chr3_137713854_r_110 110 STAG1 NM_005862 UTR chr3_58153277_r_110 110 DNASE1L3 NM_004944 INTRON OMIM: 602244 DNASE1L3 Deoxyribonuclease I-like 3 chr3_7120407_y_110 110 GRM7 NM_181875 INTRON OMIM: 604101 GRM7, MGLUR7 Glutamate receptor, metabotropic, 7 chr3_7120407_y_110 110 GRM7 NM_000844 INTRON OMIM: 604101 GRM7, MGLUR7 Glutamate receptor, metabotropic, 7 chr3_7120407_y_110 110 GRM7 NM_181874 INTRON OMIM: 604101 GRM7, MGLUR7 Glutamate receptor, metabotropic, 7 chr5_13831374_r_110 110 DNAH5 NM_001369 INTRON OMIM: 603335 DNAH5, HL1, PCD Dynein, axonemal, heavy chain 5 Primary ciliary dyskinesia, 242650 (3); Kartagener syndrome, 244400(3) MOUSE: 15(Dnahc5) chr5_156366187_r_110 110 LOC91937 NM_138379 INTRON chr5_158497667_r_110 110 EBF NM_024007 INTRON OMIM: 164343 EBF, OLF1 Early B-cell factor (olfactory neuronal transcription factor 1) MOUSE: 11(Ebf) chr5_63988067_y_110 110 FLJ36754 NM_173829 UTR chr5_70998363_y_110 110 MCCC2 NM_022132 INTRON OMIM: 210210 MCCC2, MCCB 3-Methylcrotonyl-CoA carboxylase 2 3-Methylcrotonylglycinuria II (3) chr5_82474235_y_110 110 XRCC4 NM_003401 UTR OMIM: 194363 XRCC4 X-ray repair, complementing defective, repair in Chinese hamstercells-4 between D5S427 and D5S401 chr5_82474235_y_110 110 XRCC4 NM_022406 UTR OMIM: 194363 XRCC4 X-ray repair, complementing defective, repair in Chinese hamstercells-4 between D5S427 and D5S401 chr5_82474235_y_110 110 XRCC4 NM_022550 UTR OMIM: 194363 XRCC4 X-ray repair, complementing defective, repair in Chinese hamstercells-4 between D5S427 and D5S401 chr7_121671543_r_110 110 CADPS2 NM_017954 INTRON chr7_131799465_r_110 110 FLJ40288 NM_173682 UTR chr7_726530_r_110 110 CENTA1 NM_006869 INTRON chr8_31745477_y_110 110 NRG1 NM_013962 INTRON OMIM: 142445 NRG1, HGL, HRGA, ARI Neuregulin 1 (heregulin, alpha, 45kD; ERBB2 p185-activator) {?Schizophrenia, susceptibility to}, 603013 (1) MOUSE: 7(Nrg1) chr9_92846857_r_110 110 FLJ14675 NM_032823 UTR chr10_16988782_r_111 111 CUBN NM_001081 INTRON OMIM: 602997 CUBN, IFCR, MGA1 Cubilin (intrinsic factor-cobalamin receptor) Megaloblastic anemia-1, Finnish type, 261100 (3) chr10_20307132_y_111 111 TEM7R NM_032812 INTRON OMIM: 606827 TEM7R Tumor endothelial marker 7-related protein chr12_111562631_y_111 111 RPH3A NM_014954 UTR OMIM: 604881 RPH3AL, NOC2 Rabphilin 3A-like chr12_111562752_y_111 111 RPH3A NM_014954 UTR OMIM: 604881 RPH3AL, NOC2 Rabphilin 3A-like chr12_31623915_r_111 111 MGC24039 NM_144973 INTRON chr12_6369383_r_111 111 LTBR NM_002342 INTRON OMIM: 600979 LTBR, TNFCR Lymphotoxin-beta receptor (tumor necrosis factor C receptor) tightly linked to TNFR1 in mouse MOUSE: 6(Tnfcr) chr12_99866873_y_111 111 FLJ34221 NM_178826 INTRON chr14_77013323_y_111 111 NRXN3 NM_004796 UTR OMIM: 600567 NRXN3 Neurexin 3 chr15_55084008_y_111 111 TCF12 NM_003205 INTRON OMIM: 600480 TCF12, HTF4 Transcription factor-12 (HTF4, helix-loop-helix transcriptionfactors-4) chr16_23880585_y_111 111 PRKCB1 NM_002738 INTRON OMIM: 176970 PRKCB1, PKCB Protein kinase C, beta 1 polypeptide chr17_65514584_y_111 111 CACNG4 NM_014405 INTRON chr17_77305276_r_111 111 PSCD1 NM_004762 INTRON chr17_77305276_r_111 111 PSCD1 NM_017456 INTRON chr18_48440881_r_111 111 DCC NM_005215 INTRON OMIM: 608378 SDCCAG1 Serologically defined colon cancer antigen 1 chr18_54050445_y_111 111 NEDD4L NM_015277 INTRON OMIM: 606384 NEDD4L, KIAA0439, RS Ubiquitin protein ligase NEDD4-like chr19_35649458_r_111 111 KIAA0390 NM_014717 INTRON chr19_38329178_y_111 111 LOC126248 NM_173479 INTRON chr19_60272051_r_111 111 RDH13 NM_138412 UTR chr1_173403599_r_111 111 COP1 NM_022457 INTRON OMIM: 608067 COP1 Constitutive photomorphogenesis protein, Arabidopsis, homolog of pseudogenes on chr. 3, 9, 18 chr1_234255599_y_111 111 RYR2 NM_001035 INTRON OMIM: 180902 RYR2, VTSIP Ryanodine receptor-2 (cardiac) Ventricular tachycardia, stress-induced polymorphic, 604772 (3);Arrhythmogenic r MOUSE: 13(Ryr2) chr1_61528042_r_111 111 BBP NM_032027 INTRON OMIM: 605393 RBBP2H1A Retinoblastoma-binding protein 2, homolog 1A chr20_24630228_r_111 111 C20orf39 NM_024893 INTRON chr22_40416991_y_111 111 MGC40042 NM_152513 INTRON chr2_228153625_y_111 111 COL4A4 NM_000092 INTRON OMIM: 120131 COL4A4 Collagen IV, alpha-4 polypeptide head-to-head with COL4A4 in same YAC Alport syndrome, autosomal recessive, 203780 (3); Hematuria,familial benign (3) chr2_26629927_r_111 111 MGC16372 NM_145038 INTRON chr3_125667938_y_111 111 TRAD NM_007064 INTRON OMIM: 603500 TRADD TNRF1-associated death domain protein MOUSE: 8(Tradd) chr3_40032146_r_111 111 MYRIP NM_015460 INTRON chr3_52995546_y_111 111 SFMBT NM_016329 UTR chr3_98517156_r_111 111 DKFZp434C1418 NM_173655 INTRON chr4_20556167_r_111 111 KCNIP4 NM_147181 INTRON OMIM: 608182 KCNIP4, KCHIP4 Kv channel-interacting protein 4 chr4_20556167_r_111 111 KCNIP4 NM_025221 INTRON OMIM: 608182 KCNIP4, KCHIP4 Kv channel-interacting protein 4 chr4_20556167_r_111 111 KCNIP4 NM_147183 INTRON OMIM: 608182 KCNIP4, KCHIP4 Kv channel-interacting protein 4 chr4_20556167_r_111 111 KCNIP4 NM_147182 INTRON OMIM: 608182 KCNIP4, KCHIP4 Kv channel-interacting protein 4 chr4_82104396_y_111 111 MGC35043 NM_152770 INTRON chr5_149505419_r_111 111 CSF1R NM_005211 UTR OMIM: 164770 CSF1R, FMS Colony-stimulating factor-1 receptor; oncogene FMS (McDonoughfeline sarcoma) FMS2 is 5' end Myeloid malignancy, predisposition to (3) MOUSE: 18(Fim2) chr6_131980712_y_111 111 ENPP3 NM_005021 INTRON OMIM: 602182 ENPP3, PDNP3 Ectonucleotide pyrophosphatase/phosphodiesterase 3 chr6_163600103_r_111 111 PACRG NM_152410 INTRON chr7_100606043_y_111 111 COL26A1 NM_133457 INTRON chr7_70556961_y_111 111 WBSCR17 NM_022479 INTRON chr8_143324896_r_111 111 FLJ31164 NM_145003 INTRON chr9_108083177_y_111 111 AKAP2 NM_147150 INTRON OMIM: 604582 AKAP2, AKAPKL, KIAA0 A-kinase anchor protein 2 {Longevity, reduced}, 152430 (3) chr9_108083177_y_111 111 AKAP2 NM_007203 INTRON OMIM: 604582 AKAP2, AKAPKL, KIAA0 A-kinase anchor protein 2 {Longevity, reduced}, 152430 (3) chr9_108083177_y_111 111 PALM2 NM_053016 INTRON chr9_109119940_r_111 111 EDG2 NM_057159 UTR chr9_109119940_r_111 111 EDG2 NM_001401 UTR chr9_37276925_y_111 111 FLJ22611 NM_032226 INTRON chr9_69492543_r_111 111 TRPM3 NM_024971 INTRON chrX_115977632_r_111 111 KIAA1309 NM_033495 UTR chrX_2286818_r_111 111 XG NM_175569 INTRON OMIM: 600315 TNFRSF4, TXGP1L, OX4 Tumor necrosis factor receptor superfamily, member 4 MOUSE: 4(Ox40) chr10_35038322_r_112 112 PARD3 NM_019619 INTRON OMIM: 606745 PARD3, PAR3 Partitioning-defective protein 3, C. elegans, homolog of chr10_5708497_r_112 112 ASB13 NM_024701 INTRON chr10_95565969_r_112 112 PLCE1 NM_016341 INTRON chr11_113556711_y_112 112 ZNF145 NM_006006 INTRON chr12_109069527_y_112 112 CDV-1 NM_031473 UTR chr12_109069527_y_112 112 CDV-1 NM_014055 INTRON chr12_43375137_r_112 112 NELL2 NM_006159 INTRON OMIM: 602320 NELL2 Nel-like 2 chr13_46868890_r_112 112 CHC1L NM_001268 INTRON OMIM: 603524 CHC1L Chromosome condensation 1-like chr14_66493895_y_112 112 RAD51L1 NM_133510 INTRON OMIM: 602948 RAD51L1 RAD51. S. cerevisiae, homolog of, like 1 chr14_66493895_y_112 112 RAD51L1 NM_002877 INTRON OMIM: 602948 RAD51L1 RAD51. S. cerevisiae, homolog of, like 1 chr14_66493895_y_112 112 RAD51L1 NM_133509 INTRON OMIM: 602948 RAD51L1 RAD51. S. cerevisiae, homolog of, like 1 chr14_75987803_y_112 112 SPTLC2 NM_004863 INTRON chr16_20344884_y_112 112 LOC204474 NM_174924 INTRON chr16_20413783_y_112 112 FLJ20581 NM_017888 INTRON chr17_12663058_y_112 112 FLJ34690 NM_182567 UTR chr17_16181320_r_112 112 NCOR1 NM_006311 INTRON chr17_65954885_y_112 112 PITPNC1 NM_012417 INTRON chr17_65954885_y_112 112 PITPNC1 NM_181671 INTRON chr18_17580288_y_112 112 MIB NM_020774 INTRON chr19_4102388_r_112 112 FLJ10374 NM_018074 UTR chr19_44329319_r_112 112 PAK4 NM_005884 UTR OMIM: 605451 PAK4 p21-activated kinase 4 chr1_100843642_y_112 112 SLC30A7 NM_133496 INTRON chr1_118782432_r_112 112 TBX15 NM_152380 INTRON OMIM: 604127 TBX15 T-box 15 MOUSE: 3(Tbx15) chr1_239074173_y_112 112 EXO1 NM_130398 INTRON OMIM: 606063 EXO1, HEX1 Exonuclease 1, S. cerevisiae, homolog of chr1_239074173_y_112 112 EXO1 NM_003686 INTRON OMIM: 606063 EXO1, HEX1 Exonuclease 1, S. cerevisiae, homolog of chr1_239074173_y_112 112 EXO1 NM_006027 INTRON OMIM: 606063 EXO1, HEX1 Exonuclease 1, S. cerevisiae, homolog of chr2_87034579_y_112 112 CD8B1 NM_172101 INTRON OMIM: 186730 CD8B1, CD8B CD8 antigen, beta polypeptide 1 (p37) pseudogene, CD8B2, on 2q12 MOUSE: 6(Ly3) chr2_87034579_y_112 112 CD8B1 NM_172213 INTRON OMIM: 186730 CD8B1, CD8B CD8 antigen, beta polypeptide 1 (p37) pseudogene, CD8B2, on 2q12 MOUSE: 6(Ly3) chr2_87034579_y_112 112 CD8B1 NM_172102 INTRON OMIM: 186730 CD8B1, CD8B CD8 antigen, beta polypeptide 1 (p37) pseudogene, CD8B2, on 2q12 MOUSE: 6(Ly3) chr3_115788027_y_112 112 ZNF288 NM_015642 UTR chr3_150661136_r_112 112 TAZ NM_015472 INTRON OMIM: 607392 TAZ Transcriptional coactivator with PDZ-binding motif chr3_170417176_r_112 112 MDS1 NM_004991 INTRON OMIM: 600049 MDS1 Myelodysplasia syndrome-1 cen--EVI1--MDS1--EAP--tel Myelodysplasia syndrome-1 (3) chr3_187896590_y_112 112 APM1 NM_004797 UTR OMIM: 605441 APM1, GBP28 Adiponectin (gelatin-binding protein, 28kD) conflicting assignment 1q21.3-q23 Adiponectin deficiency (3) MOUSE: 16(Apm1) chr3_188089230_r_112 112 SIAT1 NM_173216 INTRON OMIM: 109675 SIAT1 Sialyltransferase-1 (beta-galactoside alpha-2,6-sialytransferase) chr3_188089230_r_112 112 SIAT1 NM_173217 UTR OMIM: 109675 SIAT1 Sialyltransferase-1 (beta-galactoside alpha-2,6-sialytransferase) chr3_188089230_r_112 112 SIAT1 NM_003032 INTRON OMIM: 109675 SIAT1 Sialyltransferase-1 (beta-galactoside alpha-2,6-sialytransferase) chr3_6944114_r_112 112 GRM7 NM_181875 INTRON OMIM: 604101 GRM7, MGLUR7 Glutamate receptor, metabotropic, 7 chr3_6944114_r_112 112 GRM7 NM_000844 INTRON OMIM: 604101 GRM7, MGLUR7 Glutamate receptor, metabotropic, 7 chr3_6944114_r_112 112 GRM7 NM_181874 INTRON OMIM: 604101 GRM7, MGLUR7 Glutamate receptor, metabotropic, 7 chr4_40341199_y_112 112 FLJ20273 NM_019027 UTR chr4_5882882_y_112 112 EVC NM_014556 UTR OMIM: 604831 EVC Ellis-van Creveld syndrome gene Ellis-van Creveld syndrome, 225500 (3); Weyers acrodental dysostosis,193530 (3) chr4_7767438_r_112 112 SORCS2 NM_020777 INTRON OMIM: 606284 SORCS2, KIAA1329 SORCS receptor 2 chr5_16942272_r_112 112 MYO10 NM_012334 INTRON OMIM: 601481 MYO10 Myosin X MOUSE: 15(Myo10) chr6_119334224_r_112 112 C6orf60 NM_024581 UTR chr6_122826019_y_112 112 PKIB NM_181794 UTR OMIM: 606914 PKIB Protein kinase, cAMP-dependent catalytic, inhibitor beta chr6_1884154_y_112 112 GMDS NM_001500 INTRON OMIM: 602884 GMDS GDP-mannose 4,6-dehydratase chr7_110082875_y_112 112 IMMP2L NM_032549 INTRON OMIM: 605977 IMP2, IMMP2L Inner mitochondrial membrane peptidase, subunit 2, yeast, homolog of chr7_65001058_y_112 112 RCP9 NM_014478 INTRON chr8_131838756_y_112 112 ADCY8 NM_001115 INTRON OMIM: 103070 ADCY8, ADCY3 Adenylyl cyclase-8, brain chr8_70488987_r_112 112 SULF1 NM_015170 UTR chr8_99599446_r_112 112 STK3 NM_006281 INTRON OMIM: 607652 STK36, FU, KIAA1278 Serine/threonine protein kinase 36 chrX_19439932_r_112 112 FLJ14503 NM_152780 INTRON chrX_68696763_r_112 112 TEX11 NM_031276 INTRON OMIM: 300311 TEX11 Testis-expressed gene 11 chr10_53353237_y_113 113 PRKG1 NM_006258 INTRON OMIM: 176894 PRKG1, PRKG1B, PRKGR Protein kinase, cGMP-dependent, regulatory, type I chr10_95629034_r_113 113 PLCE1 NM_016341 INTRON chr11_75577401_y_113 113 UVRAG NM_003369 INTRON OMIM: 602493 UVRAG UV radiation resistance-associated gene chr11_99006837_y_113 113 CNTN5 NM_014361 INTRON OMIM: 607219 CNTN5, NB2 Contactin 5 chr11_99006837_y_113 113 CNTN5 NM_175566 INTRON OMIM: 607219 CNTN5, NB2 Contactin 5 chr12_14998085_y_113 113 ARHGDIB NM_001175 UTR OMIM: 602843 ARHGDIB, GDID4, D4 Rho GDP dissociation inhibitor (GDI) beta chr12_51902264_r_113 113 RARG NM_000966 INTRON OMIM: 180190 RARG Retinoic acid receptor, gamma polypeptide MOUSE: 15(Rarg) chr12_78173174_r_113 113 SYT1 NM_005639 INTRON OMIM: 608081 SYT15 Synaptotagmin 15 MOUSE: 14(Syt15) chr16_61474859_y_113 113 CDH8 NM_001796 INTRON OMIM: 603580 PCDH8 Protocadherin 8 MOUSE: 14(Pcdh8) chr17_16181433_r_113 113 NCOR1 NM_006311 INTRON chr17_16236755_y_113 113 NCOR1 NM_006311 INTRON chr18_3823131_y_113 113 DLGAP1 NM_004746 INTRON chr18_41489437_r_113 113 SLC14A2 NM_007163 INTRON OMIM: 601611 SLC14A2, UT2, UTR Solute carrier family 14 (urea transporter), member 2 chr19_47168754_r_113 113 ATP1A3 NM_152296 INTRON OMIM: 182350 ATP1A3 ATPase, Na+K+ transporting, alpha-3 polypeptide MOUSE: 7(Atpla3) chr19_6783482_y_113 113 TRIP10 NM_004240 UTR chr19_6783482_y_113 113 VAV1 NM_005428 INTRON OMIM: 164875 VAV1, VAV Oncogene VAV1 close to INSR chr1_165455209_y_113 113 TBX19 NM_005149 INTRON chr1_17875395_r_113 113 MGC15730 NM_032880 INTRON chr1_18032907_y_113 113 MGC15730 NM_032880 INTRON chr1_19499425_y_113 113 LOC255104 NM_181719 INTRON chr1_238440097_y_113 113 RGS7 NM_002924 INTRON chr1_31771820_r_113 113 FLJ25348 NM_144569 UTR chr1_54655659_y_113 113 FLJ40201 NM_152607 INTRON chr1_57941670_y_113 113 DAB1 NM_021080 UTR OMIM: 603448 DAB1 Disabled, Drosophila, homolog 1 MOUSE: 4(Dab1) chr20_31392183_y_113 113 HCK NM_002110 INTRON OMIM: 142370 HCK Hemopoietic cell kinase chr2_155860519_y_113 113 KCNJ3 NM_002239 INTRON OMIM: 601534 KCNJ3, GIRK1 Potassium inwardly-rectifying channel, subfamily J, member 3 chr2_179358934_y_113 113 OSBPL6 NM_032523 UTR OMIM: 606734 OSBPL6, ORP6 Oxysterol-binding protein-like protein 6 chr2_32444419_r_113 113 CARD12 NM_021209 INTRON OMIM: 606831 CARD12, CLAN, IPAF Caspase recruitment domain-containing protein 12 chr3_198002212_y_113 113 SMP3 NM_025163 INTRON OMIM: 300212 RGN, SMP30 Regucalcin chr3_199050483_y_113 113 LMLN NM_033029 INTRON chr3_31871057_r_113 113 OSBPL10 NM_017784 INTRON OMIM: 606738 OSBPL10, ORP10 Oxysterol-binding protein-like protein 10 chr3_54141259_y_113 113 CACNA2D3 NM_018398 UTR OMIM: 606399 CACNA2D3 Calcium channel, voltage-dependent, alpha-2/delta subunit 3 chr3_63419336_r_113 113 SYNPR NM_144642 INTRON chr4_21472470_r_113 113 KCNIP4 NM_147182 UTR OMIM: 608182 KCNIP4, KCHIP4 Kv channel-interacting protein 4 chr5_16944142_r_113 113 MYO10 NM_012334 INTRON OMIM: 601481 MYO10 Myosin X MOUSE: 15(Myo10) chr6_10570048_r_113 113 PAK1IP1 NM_017906 UTR chr6_158170725_y_113 113 SNX9 NM_016224 INTRON OMIM: 605952 SNX9, SH3PX1 Sorting nexin 9 chr7_146114205_r_113 113 CNTNAP2 NM_014141 INTRON OMIM: 604569 CNTNAP2, CASPR2, NRX Contactin-associated protein-like 2 chr7_40634771_y_113 113 C7orf10 NM_024728 INTRON chr7_90020191_y_113 113 PFTK1 NM_012395 INTRON chr8_63462931_r_113 113 FLJ39630 NM_173688 INTRON chr9_125098466_y_113 113 RALGPS1A NM_014636 UTR chrX_108442234_r_113 113 KIAA1318 NM_020769 UTR chrX_31413147_r_113 113 DMD NM_004013 UTR OMIM: 605512 ELOVL4, ADMD, STGD2, Elongation of very long chain fatty acids 4 Stargardt disease 3, 600110 (3); Macular dystrophy, autosomaldominant, chromosom chrX_31413147_r_113 113 DMD NM_004020 UTR OMIM: 605512 ELOVL4, ADMD, STGD2, Elongation of very long chain fatty acids 4 Stargardt disease 3, 600110 (3); Macular dystrophy, autosomaldominant, chromosom chrX_31413147_r_113 113 DMD NM_004021 UTR OMIM: 605512 ELOVL4, ADMD, STGD2, Elongation of very long chain fatty acids 4 Stargardt disease 3, 600110 (3); Macular dystrophy, autosomaldominant, chromosom chrX_31413147_r_113 113 DMD NM_004022 UTR OMIM: 605512 ELOVL4, ADMD, STGD2, Elongation of very long chain fatty acids 4 Stargardt disease 3, 600110 (3); Macular dystrophy, autosomaldominant, chromosom chrX_31413147_r_113 113 DMD NM_004023 UTR OMIM: 605512 ELOVL4, ADMD, STGD2, Elongation of very long chain fatty acids 4 Stargardt disease 3, 600110 (3); Macular dystrophy, autosomaldominant, chromosom chrX_31413147_r_113 113 DMD NM_004011 INTRON OMIM: 605512 ELOVL4, ADMD, STGD2, Elongation of very long chain fatty acids 4 Stargardt disease 3, 600110 (3); Macular dystrophy, autosomaldominant, chromosom chrX_31413147_r_113 113 DMD NM_004012 INTRON OMIM: 605512 ELOVL4, ADMD, STGD2, Elongation of very long chain fatty acids 4 Stargardt disease 3, 600110 (3); Macular dystrophy, autosomaldominant, chromosom chrX_31413147_r_113 113 DMD NM_004007 INTRON OMIM: 605512 ELOVL4, ADMD, STGD2, Elongation of very long chain fatty acids 4 Stargardt disease 3, 600110 (3); Macular dystrophy, autosomaldominant, chromosom chrX_31413147_r_113 113 DMD NM_004009 INTRON OMIM: 605512 ELOVL4, ADMD, STGD2, Elongation of very long chain fatty acids 4 Stargardt disease 3, 600110 (3); Macular dystrophy, autosomaldominant, chromosom chrX_31413147_r_113 113 DMD NM_004010 INTRON OMIM: 605512 ELOVL4, ADMD, STGD2, Elongation of very long chain fatty acids 4 Stargardt disease 3, 600110 (3); Macular dystrophy, autosomaldominant, chromosom chrX_31413147_r_113 113 DMD NM_004006 INTRON OMIM: 605512 ELOVL4, ADMD, STGD2, Elongation of very long chain fatty acids 4 Stargardt disease 3, 600110 (3); Macular dystrophy, autosomaldominant, chromosom chrX_31413147_r_113 113 DMD NM_000109 INTRON OMIM: 605512 ELOVL4, ADMD, STGD2, Elongation of very long chain fatty acids 4 Stargardt disease 3, 600110 (3); Macular dystrophy, autosomaldominant, chromosom chrX_66281599_r_113 113 OPHN1 NM_002547 INTRON OMIM: 300127 OPHN1 Oligophrenin-1 Mental retardation, X-linked, 60 (3) chr10_13796000_r_114 114 FLJ10210 NM_018027 INTRON chr10_23624551_r_114 114 MGC46732 NM_153714 INTRON chr10_53353372_y_114 114 PRKG1 NM_006258 INTRON OMIM: 176894 PRKG1, PRKG1B, PRKGR Protein kinase, cGMP-dependent, regulatory, type I chr10_70333223_r_114 114 FLJ22761 NM_025130 INTRON chr10_71266714_r_114 114 SARA1 NM_020150 UTR OMIM: 607691 SARA1, SAR1A Sar1a, S. cerevisiae, homolog 1 chr11_70172275_r_114 114 SHANK2 NM_012309 INTRON OMIM: 603290 SHANK2, CORTBP1 SH3 and multiple ankyrin repeat domains 2 chr11_70172275_r_114 114 SHANK2 NM_133266 INTRON OMIM: 603290 SHANK2, CORTBP1 SH3 and multiple ankyrin repeat domains 2 chr11_86632647_y_114 114 FLJ22104 NM_022918 INTRON chr12_121734795_r_114 114 TSP-NY NM_032573 INTRON chr15_83201527_y_114 114 SLC28A1 NM_004213 INTRON OMIM: 606207 SLC28A1, CNT1 Solute carrier family 28 (sodium-coupled nucleoside transporter),member 1 chr16_8799077_r_114 114 ABAT NM_000663 INTRON OMIM: 137165 SLC6A1, GABATR Solute carrier family 6 (neurotransmitter transporter, GABA), member 1 chr1_198477443_y_114 114 DKFZp434B1231 NM_178275 INTRON chr20_45940273_y_114 114 SLC13A3 NM_022829 INTRON OMIM: 606411 SLC13A3, NADC3 Solute carrier family 13 (sodium-dependent dicarboxylate transporter),member 3 chr21_36552881_r_114 114 C21orf5 NM_005128 INTRON OMIM: 604803 C21orf5, KIAA0933 Chromosome 21 open reading frame 5 chr2_125272618_y_114 114 caspr5 NM_130773 INTRON chr2_125272618_y_114 114 caspr5 NM_138996 INTRON chr2_125391236_r_114 114 caspr5 NM_130773 INTRON chr2_125391236_r_114 114 caspr5 NM_138996 INTRON chr3_106528397_r_114 114 ALCAM NM_001627 INTRON OMIM: 601662 ALCAM Activated leucocyte cell adhesion molecule chr3_125668050_y_114 114 TRAD NM_007064 INTRON OMIM: 603500 TRADD TNRF1-associated death domain protein MOUSE: 8(Tradd) chr3_186568582_r_114 114 LIPH NM_139248 INTRON OMIM: 607365 LIPH Lipase H chr3_54813017_y_114 114 CACNA2D3 NM_018398 INTRON OMIM: 606399 CACNA2D3 Calcium channel, voltage-dependent, alpha-2/delta subunit 3 chr4_21152971_y_114 114 KCNIP4 NM_147182 UTR OMIM: 608182 KCNIP4, KCHIP4 Kv channel-interacting protein 4 chr4_7361029_y_114 114 SORCS2 NM_020777 INTRON OMIM: 606284 SORCS2, KIAA1329 SORCS receptor 2 chr5_13895253_r_114 114 DNAH5 NM_001369 INTRON OMIM: 603335 DNAH5, HL1, PCD Dynein, axonemal, heavy chain 5 Primary ciliary dyskinesia, 242650 (3); Kartagener syndrome, 244400(3) MOUSE: 15(Dnahc5) chr5_45518154_r_114 114 HCN1 NM_021072 INTRON chr6_24750221_r_114 114 KIAA0319 NM_014809 UTR chr6_45093995_r_114 114 SUPT3H NM_003599 INTRON chr7_102170775_r_114 114 MGC21636 NM_145032 INTRON chr7_14447516_y_114 114 DGKB NM_004080 INTRON OMIM: 604070 DGKB, DGK Diacylglycerol kinase, beta, 90kD chr7_14447516_y_114 114 DGKB NM_145695 INTRON OMIM: 604070 DGKB, DGK Diacylglycerol kinase, beta, 90kD chr7_43954952_y_114 114 GCK NM_000162 INTRON OMIM: 600842 GCKR, GKRP Glucokinase (hexokinase 4) regulatory protein chr7_47158054_y_114 114 TEM6 NM_022748 INTRON OMIM: 606825 TEM6 Tumor endothelial marker 6 chr7_70557308_y_114 114 WBSCR17 NM_022479 INTRON chr7_99985649_y_114 114 ZAN NM_003386 INTRON OMIM: 602372 ZAN Zonadhesin MOUSE: 5(Zan) chr7_99985649_y_114 114 ZAN NM_173055 INTRON OMIM: 602372 ZAN Zonadhesin MOUSE: 5(Zan) chr7_99985649_y_114 114 ZAN NM_173056 INTRON OMIM: 602372 ZAN Zonadhesin MOUSE: 5(Zan) chr7_99985649_y_114 114 ZAN NM_173057 INTRON OMIM: 602372 ZAN Zonadhesin MOUSE: 5(Zan) chr7_99985649_y_114 114 ZAN NM_173058 INTRON OMIM: 602372 ZAN Zonadhesin MOUSE: 5(Zan) chr7_99985649_y_114 114 ZAN NM_173059 INTRON OMIM: 602372 ZAN Zonadhesin MOUSE: 5(Zan) chr8_143198423_r_114 114 FLJ31164 NM_145003 UTR chr9_111472238_y_114 114 LOC114987 NM_145241 UTR chr9_125648085_y_114 114 DKFZP434H0820 NM_022833 INTRON chrX_146468672_r_114 114 FMR2 NM_002025 INTRON OMIM: 309548 FMR2, FRAXE, MRX2 Fragile site, X-linked, E Mental retardation, X-linked, FRAXE type (3) chr10_122673956_r_115 115 FGFR2 NM_022971 UTR OMIM: 176943 FGFR2, BEK, CFD1, JW Fibroblast growth factor receptor-2 (bacteria-expressed kinase) Crouzon syndrome, 123500 (3); Jackson-Weiss syndrome, 123150 (3);Beare-Stevenson MOUSE: 7(Fgfr2) chr10_78543430_r_115 115 KCNMA1 NM_002247 INTRON OMIM: 600150 KCNMA1, SLO Potassium large conductance calcium-activated channel, subfamily M,alpha member chr11_108153408_y_115 115 DDX10 NM_004398 INTRON OMIM: 601235 DDX10 DEAD/H box-10 (RNA helicase) 400kb telomeric to ATM; pseudogene on 9q21-q22; fused with NUP98 inAML chr16_23186509_y_115 115 SCNN1G NM_001039 INTRON OMIM: 600761 SCNN1G, PHA1 Sodium channel, nonvoltage-gated 1, gamma same 400kb fragment as SCNN1B Liddle syndrome, 177200 (3); Pseudohypoaldosteronism, type I, 264350(3) MOUSE: 7(Scnn1g) chr18_42556917_r_115 115 SIAT8E NM_013305 INTRON OMIM: 607162 SIAT8E Sialyltransferase 8E chr18_61646715_y_115 115 CDH7 NM_033646 INTRON OMIM: 602988 PCDH7, BHPCDH Protocadherin-7 chr18_61646715_y_115 115 CDH7 NM_004361 INTRON OMIM: 602988 PCDH7, BHPCDH Protocadherin-7 chr19_43666832_y_115 115 RYR1 NM_000540 INTRON OMIM: 180901 RYR1, MHS, CCO Ryanodine receptor-1, skeletal {Malignant hyperthermia susceptibility 1}, 145600 (3); Central coredisease, 1170 MOUSE: 7(Ryr) chr1_65204126_y_115 115 DNAJC6 NM_014787 INTRON OMIM: 608375 DNAJC6, DJC6, KIAA04 DNAJ, E. coli, homolog of, subfamily C, member 6 chr20_52452607_r_115 115 FLJ33887 NM_173485 INTRON chr2_162719611_y_115 115 SLC4A10 NM_022058 INTRON OMIM: 605556 SLC4A10 Solute carrier family 4 (sodium bicarbonate cotransporter-like),member 10 chr2_238592794_r_115 115 COL6A3 NM_004369 UTR OMIM: 120250 COL6A3 Collagen VI, alpha-3 polypeptide close to CRBP1 Bethlem myopathy, 158810 (3); Ullrich congenital muscular dystrophy,254090 (3) MOUSE: 1(Col6a3) chr2_238592794_r_115 115 COL6A3 NM_057164 UTR OMIM: 120250 COL6A3 Collagen VI, alpha-3 polypeptide close to CRBP1 Bethlem myopathy, 158810 (3); Ullrich congenital muscular dystrophy,254090 (3) MOUSE: 1(Col6a3) chr2_238592794_r_115 115 COL6A3 NM_057165 UTR OMIM: 120250 COL6A3 Collagen VI, alpha-3 polypeptide close to CRBP1 Bethlem myopathy, 158810 (3); Ullrich congenital muscular dystrophy,254090 (3) MOUSE: 1(Col6a3) chr2_238592794_r_115 115 COL6A3 NM_057166 UTR OMIM: 120250 COL6A3 Collagen VI, alpha-3 polypeptide close to CRBP1 Bethlem myopathy, 158810 (3); Ullrich congenital muscular dystrophy,254090 (3) MOUSE: 1(Col6a3) chr2_238592794_r_115 115 COL6A3 NM_057167 UTR OMIM: 120250 COL6A3 Collagen VI, alpha-3 polypeptide close to CRBP1 Bethlem myopathy, 158810 (3); Ullrich congenital muscular dystrophy,254090 (3) MOUSE: 1(Col6a3) chr3_191157806_r_115 115 MLAT4 NM_018192 INTRON chr3_198994957_y_115 115 DKFZp434B227 NM_032263 INTRON chr3_42095692_y_115 115 OIP106 NM_014965 INTRON OMIM: 608112 OIP106, KIAA1042 OGT-interacting protein, 106kD chr4_158729275_y_115 115 GRIA2 NM_000826 INTRON OMIM: 138247 GRIA2, GLUR2 Glutamate receptor, ionotropic, AMPA 2 MOUSE: 3(Glur2) chr4_62301654_y_115 115 LPHN3 NM_015236 UTR chr5_131012436_r_115 115 RA-GEF-2 NM_016340 INTRON chr6_38281208_r_115 115 BTBD9 NM_152733 INTRON chr6_46812442_y_115 115 MEP1A NM_005588 INTRON OMIM: 600388 MEP1A Meprin A, alpha MOUSE: 17(Mep1a) chr7_35620976_y_115 115 CDC10 NM_001788 INTRON chr7_43246282_r_115 115 KIAA0322 NM_015052 INTRON chr8_68510351_y_115 115 CPA6 NM_020361 INTRON chr9_33929992_r_115 115 UBAP2 NM_018449 INTRON chr9_33929992_r_115 115 UBAP2 NM_020867 INTRON chr9_33929992_r_115 115 UBAP2 NM_148171 UTR chr9_8601727_r_115 115 PTPRD NM_002839 INTRON OMIM: 601598 PTPRD, PTPD, HPTP Protein tyrosine phosphatase, receptor type, delta polypeptide MOUSE: 4(Ptprd) chr9_8601727_r_115 115 PTPRD NM_130391 INTRON OMIM: 601598 PTPRD, PTPD, HPTP Protein tyrosine phosphatase, receptor type, delta polypeptide MOUSE: 4(Ptprd) chr9_8601727_r_115 115 PTPRD NM_130392 INTRON OMIM: 601598 PTPRD, PTPD, HPTP Protein tyrosine phosphatase, receptor type, delta polypeptide MOUSE: 4(Ptprd) chr9_8601727_r_115 115 PTPRD NM_130393 INTRON OMIM: 601598 PTPRD, PTPD, HPTP Protein tyrosine phosphatase, receptor type, delta polypeptide MOUSE: 4(Ptprd) chr10_16956172_y_116 116 CUBN NM_001081 INTRON OMIM: 602997 CUBN, IFCR, MGA1 Cubilin (intrinsic factor-cobalamin receptor) Megaloblastic anemia-1, Finnish type, 261100 (3) chr10_78255439_y_116 116 KCNMA1 NM_002247 INTRON OMIM: 600150 KCNMA1, SLO Potassium large conductance calcium-activated channel, subfamily M,alpha member chr10_91179729_y_116 116 MPHOSPH1 NM_016195 INTRON OMIM: 605498 MPHOSPH1, MPP1 M-phase phosphoprotein 1 chr11_62039631_r_116 116 MGC5395 NM_024060 INTRON chr12_115644363_r_116 116 FLJ14627 NM_032814 INTRON chr12_7704166_r_116 116 APOBEC1 NM_001644 INTRON OMIM: 600130 APOBEC1, BEDP Apolipoprotein B mRNA editing enzyme, catalytic polypeptide 1 chr12_7704166_r_116 116 APOBEC1 NM_005889 INTRON OMIM: 600130 APOBEC1, BEDP Apolipoprotein B mRNA editing enzyme, catalytic polypeptide 1 chr12_94592144_y_116 116 NTN4 NM_021229 INTRON OMIM: 607280 CNTN4 Contactin 4 chr16_55656604_y_116 116 FLJ31547 NM_145024 INTRON chr16_71192130_r_116 116 CALB2 NM_001740 INTRON OMIM: 114051 CALB2 Calbindin 2, 29kD (calretinin) chr16_71192130_r_116 116 CALB2 NM_007087 INTRON OMIM: 114051 CALB2 Calbindin 2, 29kD (calretinin) chr16_71192130_r_116 116 CALB2 NM_007088 INTRON OMIM: 114051 CALB2 Calbindin 2, 29kD (calretinin) chr17_28687512_y_116 116 SLC6A4 NM_001045 INTRON OMIM: 182138 SLC6A4, HTT Solute carrier family 6 (neurotransmitter transporter, serotonin),member 4 Anxiety-related personality traits (3) MOUSE: 11(Htt) chr18_54751511_y_116 116 FLJ10697 NM_018181 INTRON chr19_60337872_r_116 116 TNNT1 NM_003283 INTRON OMIM: 191041 TNNT1, ANM Troponin-T1, skeletal, slow Nemaline myopathy, Amish type, 605355 (3) chr1_16942708_r_116 116 PADI1 NM_013358 INTRON chr1_207017911_r_116 116 DJ434O14.3 NM_025228 INTRON chr1_49969150_r_116 116 ELAVL4 NM_021952 INTRON OMIM: 168360 ELAVL4, HUD, PNEM Embryonic lethal, abnormal vision, Drosophila, homolog of, like-4(Hu antigen D) Neuropathy, paraneoplastic sensory (1) MOUSE: 4(Hud) chr20_36238082_r_116 116 SAMHD1 NM_015474 INTRON chr20_47943760_r_116 116 PRex1 NM_020820 INTRON chr22_37597804_y_116 116 APOBEC3A NM_145699 INTRON OMIM: 607109 APOBEC3A, PHRBN Apolipoprotein B mRNA editing enzyme, catalytic polypeptide-like 3A(phorbolin 1) chr22_44197578_r_116 116 FBLN1 NM_006487 INTRON OMIM: 135820 FBLN1 Fibulin 1 Synpolydactyly, 3/3'4, associated with metacarpal and metatarsalsynostoses, 6081 MOUSE: 15(Fbln1) chr22_44197578_r_116 116 FBLN1 NM_001996 INTRON OMIM: 135820 FBLN1 Fibulin 1 Synpolydactyly, 3/3'4, associated with metacarpal and metatarsalsynostoses, 6081 MOUSE: 15(Fbln1) chr22_44197578_r_116 116 FBLN1 NM_006485 INTRON OMIM: 135820 FBLN1 Fibulin 1 Synpolydactyly, 3/3'4, associated with metacarpal and metatarsalsynostoses, 6081 MOUSE: 15(Fbln1) chr22_44197578_r_116 116 FBLN1 NM_006486 INTRON OMIM: 135820 FBLN1 Fibulin 1 Synpolydactyly, 3/3'4, associated with metacarpal and metatarsalsynostoses, 6081 MOUSE: 15(Fbln1) chr2_80131909_r_116 116 CTNNA2 NM_004389 INTRON OMIM: 114025 CTNNA2, CAPR, CTNR Catenin, alpha-2 (cadherin-associated protein, related) MOUSE: 6(Capr) chr2_80508026_y_116 116 CTNNA2 NM_004389 INTRON OMIM: 114025 CTNNA2, CAPR, CTNR Catenin, alpha-2 (cadherin-associated protein, related) MOUSE: 6(Capr) chr4_30712572_r_116 116 PCDH7 NM_032457 INTRON OMIM: 602988 PCDH7, BHPCDH Protocadherin-7 chr4_68439755_r_116 116 BRDG1 NM_012108 INTRON chr5_173488393_y_116 116 HMP19 NM_015980 INTRON chr5_79608118_r_116 116 TPO1 NM_178276 INTRON chr7_151874202_r_116 116 ARP3BETA NM_020445 INTRON chr7_2717716_y_116 116 CARD11 NM_032415 INTRON chr7_37037249_r_116 116 ELMO1 NM_014800 INTRON OMIM: 606420 ELMO1, CED12 Engulfment and cell motility gene 1 chr7_97380787_y_116 116 KPI2 NM_014916 INTRON chr8_26386867_r_116 116 PNMA2 NM_007257 UTR chr8_27283244_y_116 116 PTK2B NM_004103 INTRON OMIM: 601212 PTK2B, FAK2, PYK2 Protein tyrosine kinase-2, beta (focal adhesion kinase 2) chr8_27283244_y_116 116 PTK2B NM_173174 INTRON OMIM: 601212 PTK2B, FAK2, PYK2 Protein tyrosine kinase-2, beta (focal adhesion kinase 2) chr8_27283244_y_116 116 PTK2B NM_173176 INTRON OMIM: 601212 PTK2B, FAK2, PYK2 Protein tyrosine kinase-2, beta (focal adhesion kinase 2) chr8_27283244_y_116 116 PTK2B NM_173175 INTRON OMIM: 601212 PTK2B, FAK2, PYK2 Protein tyrosine kinase-2, beta (focal adhesion kinase 2) chr8_62668925_r_116 116 ASPH NM_004318 INTRON OMIM: 600582 ASPH, HAAH Aspartate beta-hydroxylase (junctin; junctate) chr8_62668925_r_116 116 ASPH NM_032466 INTRON OMIM: 600582 ASPH, HAAH Aspartate beta-hydroxylase (junctin; junctate) chr10_115925025_r_117 117 ABLIM1 NM_006720 UTR chr10_115925025_r_117 117 ABLIM1 NM_006719 INTRON chr10_115925025_r_117 117 ABLIM1 NM_002313 INTRON chr10_12873606_y_117 117 CKLiK NM_153498 INTRON chr15_59106318_y_117 117 RORA NM_134261 INTRON OMIM: 600825 RORA RAR-related orphan receptor A MOUSE: 9(Rora) chr15_87162959_r_117 117 HAPLN3 NM_178232 UTR chr16_24329534_r_117 117 CACNG3 NM_006539 INTRON OMIM: 606403 CACNG3 Calcium channel, voltage-dependent, gamma-3 subunit chr17_42829256_y_117 117 UBTF NM_014233 UTR OMIM: 600673 UBTF, UBF Upstream binding transcription factor, RNA polymerase I chr17_74913458_r_117 117 PRPSAP1 NM_002766 INTRON OMIM: 601249 PRPSAP1 Phosphoribosyl pyrophosphate synthetase-associated protein-1 chr18_22885035_r_117 117 CHST9 NM_031422 INTRON chr19_12453725_r_117 117 FLJ38281 NM_152601 UTR chr19_2538840_r_117 117 FLJ00058 NM_052847 UTR chr1_108135523_y_117 117 FLJ32833 NM_152488 UTR chr1_148585851_y_117 117 CGN NM_020770 UTR OMIM: 600621 STMN2, SCGN10, SCG10 Stathmin-like 2 chr21_40446463_y_117 117 DSCAM NM_001389 INTRON OMIM: 602523 DSCAM Down syndrome cell adhesion molecule chr2_17788278_r_117 117 VSNL1 NM_003385 INTRON OMIM: 600817 VSNL1 Visinin-like 1 chr3_173080062_y_117 117 FAD104 NM_022763 UTR chr3_196811230_y_117 117 MUC4 NM_004532 INTRON OMIM: 158372 MUC4 Mucin 4, tracheobronchial chr3_196811230_y_117 117 MUC4 NM_138297 INTRON OMIM: 158372 MUC4 Mucin 4, tracheobronchial chr3_196811230_y_117 117 MUC4 NM_018406 INTRON OMIM: 158372 MUC4 Mucin 4, tracheobronchial chr3_196811230_y_117 117 MUC4 NM_138298 UTR OMIM: 158372 MUC4 Mucin 4, tracheobronchial chr3_196811230_y_117 117 MUC4 NM_138299 INTRON OMIM: 158372 MUC4 Mucin 4, tracheobronchial chr4_108362897_r_117 117 DKK2 NM_014421 INTRON chr4_20839393_y_117 117 KCNIP4 NM_147183 INTRON OMIM: 608182 KCNIP4, KCHIP4 Kv channel-interacting protein 4 chr4_20839393_y_117 117 KCNIP4 NM_147182 UTR OMIM: 608182 KCNIP4, KCHIP4 Kv channel-interacting protein 4 chr4_21074540_r_117 117 KCNIP4 NM_147182 UTR OMIM: 608182 KCNIP4, KCHIP4 Kv channel-interacting protein 4 chr4_62317892_r_117 117 LPHN3 NM_015236 UTR chr4_72065035_r_117 117 RIPX NM_014961 INTRON chr4_96341588_y_117 117 BMPR1B NM_001203 UTR OMIM: 603248 BMPR1B, ALK6 Bone morphogenetic protein receptor, type IB chr5_167810901_y_117 117 KIBRA NM_015238 INTRON chr5_24177945_r_117 117 FLJ34836 NM_173668 UTR chr5_39052281_r_117 117 MGC39830 NM_152756 INTRON chr6_129686764_r_117 117 LAMA2 NM_000426 INTRON OMIM: 156225 LAMA2, LAMM Laminin, alpha-2 (merosin) Muscular dystrophy, congenital merosin-deficient, 607855 (3);Muscular dystrophy, MOUSE: 10(dy, Lamm) chr6_154451527_r_117 117 OPRM1 NM_000914 INTRON OMIM: 600018 OPRM1 Opioid receptor, mu-1 [Response to morphine-6-glucuronide] (3) MOUSE: 10(Oprm) chr7_102035011_r_117 117 MGC21636 NM_145032 INTRON chr7_125840765_r_117 117 GRM8 NM_000845 INTRON OMIM: 601116 GRM8 Glutamate receptor, metabotropic-8 chr7_35619083_y_117 117 CDC10 NM_001788 INTRON chr9_125320657_y_117 117 RALGPS1A NM_014636 INTRON chrX_105925855_y_117 117 MID2 NM_012216 INTRON OMIM: 300204 MID2 Midline 2 MOUSE: X(Mid2) chrX_105925855_y_117 117 MID2 NM_052817 INTRON OMIM: 300204 MID2 Midline 2 MOUSE: X(Mid2) chrX_134320340_y_117 117 VGLL1 NM_016267 UTR chrX_19027807_r_117 117 SH3KBP1 NM_031892 INTRON OMIM: 300374 SH3KBP1, CIN85 SH3-domain kinase-binding protein 1 chr10_55801973_r_118 118 PCDH15 NM_033056 UTR OMIM: 605514 PCDH15 Protocadherin 15 Usher syndrome, type 1F, 602083 (3) MOUSE: 10(av) chr10_78437712_r_118 118 KCNMA1 NM_002247 INTRON OMIM: 600150 KCNMA1, SLO Potassium large conductance calcium-activated channel, subfamily M,alpha member chr10_98675850_r_118 118 MGC14258 NM_032900 INTRON chr11_2815505_r_118 118 KCNQ1 NM_000218 INTRON OMIM: 607542 KCNQ1, KCNA9, LQT1, Potassium voltage-gated channel, KQT-like subfamily, member 1 Long QT syndrome-1, 192500 (3); Jervell and Lange-Nielsen syndrome,220400 (3); A chr11_2815505_r_118 118 KCNQ1 NM_181797 INTRON OMIM: 607542 KCNQ1, KCNA9, LQT1, Potassium voltage-gated channel, KQT-like subfamily, member 1 Long QT syndrome-1, 192500 (3); Jervell and Lange-Nielsen syndrome,220400 (3); A chr11_2815505_r_118 118 KCNQ1 NM_181798 INTRON OMIM: 607542 KCNQ1, KCNA9, LQT1, Potassium voltage-gated channel, KQT-like subfamily, member 1 Long QT syndrome-1, 192500 (3); Jervell and Lange-Nielsen syndrome,220400 (3); A chr12_2551724_y_118 118 CACNA1C NM_000719 INTRON OMIM: 114205 CACNA1C, CACNL1A1, C Calcium channel, voltage-dependent, L type, alpha 1C subunit chr12_76860069_y_118 118 NAV3 NM_014903 INTRON chr12_93489604_r_118 118 KIAA1145 NM_020698 INTRON chr13_72177742_r_118 118 KLF12 NM_007249 INTRON OMIM: 607531 KLF12, AP2REP Kruppel-like factor 12 chr14_76913156_y_118 118 NRXN3 NM_004796 UTR OMIM: 600567 NRXN3 Neurexin 3 chr15_24466909_r_118 118 GABRB3 NM_000814 INTRON OMIM: 137192 GABRB3 Gamma-aminobutyric acid (GABA) A receptor, beta-3 ?Insomnia (3) MOUSE: 7(Gabrb3) chr15_24466909_r_118 118 GABRB3 NM_021912 INTRON OMIM: 137192 GABRB3 Gamma-aminobutyric acid (GABA) A receptor, beta-3 ?Insomnia (3) MOUSE: 7(Gabrb3) chr15_59068191_r_118 118 RORA NM_134261 INTRON OMIM: 600825 RORA RAR-related orphan receptor A MOUSE: 9(Rora) chr15_70022842_r_118 118 MYO9A NM_006901 INTRON OMIM: 604875 MYO9A Myosin IXa chr16_80485948_r_118 118 CDYL2 NM_152342 INTRON chr17_40259431_r_118 118 HAP1 NM_003949 INTRON OMIM: 600832 ANP32A, PHAP1 Acidic (leucine-rich) nuclear phosphoprotein 32 family, member A chr17_40259431_r_118 118 HAP1 NM_177977 INTRON OMIM: 600832 ANP32A, PHAP1 Acidic (leucine-rich) nuclear phosphoprotein 32 family, member A chr19_15622587_y_118 118 CYP4F3 NM_000896 INTRON OMIM: 601270 CYP4F3, LTB4H Cytochrome P450, subfamily IVF, polypeptide 3 chr19_53218586_r_118 118 ELSPBP1 NM_022142 UTR chr19_9872763_r_118 118 OLFM2 NM_058164 INTRON chr1_76229882_y_118 118 Siat7c NM_152996 INTRON chr20_34202858_y_118 118 ACAS2 NM_139274 INTRON chr20_34202858_y_118 118 ACAS2 NM_018677 INTRON chr21_32741596_r_118 118 C21orf63 NM_058187 INTRON chr3_170225008_r_118 118 MDS1 NM_004991 INTRON OMIM: 600049 MDS1 Myelodysplasia syndrome-1 cen--EVI1--MDS1--EAP--tel Myelodysplasia syndrome-1 (3) chr3_29814706_r_118 118 RBMS3 NM_014483 INTRON OMIM: 605786 RBMS3 RNA-binding motif protein, single strand-interacting, 3 chr3_52772549_y_118 118 ITIH1 NM_002215 INTRON OMIM: 147270 ITIH1 Inter-alpha (globulin) inhibitor, H1 polypeptide MOUSE: 14(Intin1) chr3_63419093_r_118 118 SYNPR NM_144642 INTRON chr4_5169110_y_118 118 HSA250839 NM_018401 INTRON chr5_106811236_r_118 118 EFNA5 NM_001962 INTRON chr6_51901507_r_118 118 PKHD1 NM_138694 INTRON OMIM: 606702 FCYT, PKHD1, ARPKD Fibrocystin Polycystic kidney and hepatic disease, 263200 (3) MOUSE: 13(Pkhd1) chr6_51901507_r_118 118 PKHD1 NM_170724 INTRON OMIM: 606702 FCYT, PKHD1, ARPKD Fibrocystin Polycystic kidney and hepatic disease, 263200 (3) MOUSE: 13(Pkhd1) chr8_114379713_r_118 118 CSMD3 NM_052900 INTRON OMIM: 608399 CSMD3, KIAA1894 Cub and Sushi multiple domains 3 chr9_108148385_y_118 118 AKAP2 NM_147150 INTRON OMIM: 604582 AKAP2, AKAPKL, KIAA0 A-kinase anchor protein 2 {Longevity, reduced}, 152430 (3) chr9_108148385_y_118 118 AKAP2 NM_007203 INTRON OMIM: 604582 AKAP2, AKAPKL, KIAA0 A-kinase anchor protein 2 {Longevity, reduced}, 152430 (3) chr9_115232460_r_118 118 ASTN2 NM_014010 UTR chr9_81735126_r_118 118 UBQLN1 NM_013438 INTRON OMIM: 605046 UBQLN1, DA41 Ubiquilin 1 (Da41, rat, homolog of) chr9_81735126_r_118 118 UBQLN1 NM_053067 INTRON OMIM: 605046 UBQLN1, DA41 Ubiquilin 1 (Da41, rat, homolog of) chrX_10167022_y_118 118 MID1 NM_033290 UTR OMIM: 300000 MID1, OGS1, BBBG1, F Midline-1 type II defect on chr.22 Opitz G syndrome, type I (3) MOUSE: X(Mid1) chrX_46513598_r_118 118 SYN1 NM_006950 INTRON OMIM: 608285 NADSYN1 NAD synthetase 1 chrX_46513598_r_118 118 SYN1 NM_133499 INTRON OMIM: 608285 NADSYN1 NAD synthetase 1 chrX_8174674_y_118 118 FAM9A NM_174951 EXON chr10_23303566_y_119 119 FLJ32827 NM_173081 INTRON chr10_75404620_y_119 119 ADK NM_006721 INTRON OMIM: 600758 PTK2, FADK PTK2 protein tyrosine kinase MOUSE: 15(Fadk) chr10_75404620_y_119 119 ADK NM_001123 INTRON OMIM: 600758 PTK2, FADK PTK2 protein tyrosine kinase MOUSE: 15(Fadk) chr10_81936043_y_119 119 DC-TM4F2 NM_030927 INTRON chr10_93436487_y_119 119 BTAF1 NM_003972 INTRON OMIM: 605191 BTAF1, TAFII170, TAF BTAF1 RNA polymerase II, B-TFIID transcription factor-associated,170kD (Mot1, S. chr11_110761317_r_119 119 POU2AF1 NM_006235 UTR OMIM: 601206 POU2AF1, OBF1 POU domain, class 2, associating factor 1 chr11_122558777_r_119 119 ASAM NM_024769 INTRON chr12_121940055_y_119 119 PITPNM2 NM_020845 INTRON chr12_13723158_r_119 119 GRIN2B NM_000834 INTRON OMIM: 138252 GRIN2B, NMDAR2B Glutamate receptor, ionotropic, N-methyl D-aspartate 2B MOUSE: 6(Nmdar2b) chr13_71345425_r_119 119 PIBF1 NM_006346 INTRON OMIM: 607532 PIBF1 Progesterone-induced blocking factor 1 chr16_19519508_r_119 119 MGC16824 NM_020314 UTR chr16_19519508_r_119 119 CP110 NM_014711 INTRON chr17_41502787_r_119 119 MGC2744 NM_025267 INTRON chr17_65966556_y_119 119 PITPNC1 NM_012417 INTRON chr17_65966556_y_119 119 PITPNC1 NM_181671 INTRON chr19_3199837_y_119 119 BRUNOL5 NM_021938 INTRON chr19_45532706_r_119 119 FLJ36888 NM_178830 INTRON chr1_165165914_y_119 119 PC326 NM_018442 INTRON chr1_167847960_y_119 119 PMX1 NM_006902 INTRON OMIM: 167420 PMX1, PHOX1 Paired mesoderm homeo box 1 MOUSE: 1(Pmx) chr1_167847960_y_119 119 PMX1 NM_022716 INTRON OMIM: 167420 PMX1, PHOX1 Paired mesoderm homeo box 1 MOUSE: 1(Pmx) chr20_32368993_r_119 119 RYA3 NM_182658 INTRON chr20_44739174_y_119 119 PIGT NM_015937 INTRON chr20_63590791_y_119 119 MYT1 NM_004535 INTRON chr21_29171177_r_119 119 N6AMT1 NM_013240 INTRON chr2_100185348_r_119 119 LAF4 NM_002285 INTRON OMIM: 601464 LAF4 Lymphoid nuclear protein related to AF4 MOUSE: 1(Laf4) chr2_10817072_r_119 119 FLJ14075 NM_024894 INTRON chr2_202904673_r_119 119 ALS2CR7 NM_139158 INTRON chr2_30956144_y_119 119 CAPN13 NM_144575 INTRON chr2_30997475_r_119 119 CAPN13 NM_144575 UTR chr2_36735971_r_119 119 CRIM1 NM_016441 INTRON OMIM: 606189 CRIM1 Cysteine-rich motor neuron protein 1 chr3_124860359_y_119 119 MYLK NM_053025 UTR OMIM: 600922 MYLK, MLCK Myosin-light-polypeptide kinase pseudogene on 3p13 chr3_124860359_y_119 119 MYLK NM_053026 UTR OMIM: 600922 MYLK, MLCK Myosin-light-polypeptide kinase pseudogene on 3p13 chr3_124860359_y_119 119 MYLK NM_053027 UTR OMIM: 600922 MYLK, MLCK Myosin-light-polypeptide kinase pseudogene on 3p13 chr3_124860359_y_119 119 MYLK NM_053028 UTR OMIM: 600922 MYLK, MLCK Myosin-light-polypeptide kinase pseudogene on 3p13 chr3_124860359_y_119 119 MYLK NM_053029 UTR OMIM: 600922 MYLK, MLCK Myosin-light-polypeptide kinase pseudogene on 3p13 chr3_1349152_r_119 119 CNTN6 NM_014461 INTRON OMIM: 607220 CNTN6, NB3 Contactin 6 chr4_124397112_r_119 119 SPATA5 NM_145207 INTRON chr4_26137412_y_119 119 KBF2 NM_015874 UTR chr4_26137412_y_119 119 RBPSUH NM_005349 UTR chr4_80209303_y_119 119 BMP2K NM_017593 INTRON chr5_158458048_y_119 119 EBF NM_024007 INTRON OMIM: 164343 EBF, OLF1 Early B-cell factor (olfactory neuronal transcription factor 1) MOUSE: 11(Ebf) chr5_176566162_y_119 119 NSD1 NM_022455 INTRON OMIM: 606681 NSD1, ARA267, STO Nuclear receptor binding SET domain protein 1 fusion gene with NUP98 in AML Sotos syndrome, 117550 (3); Leukemia, acute myeloid, 601626 (1);Weaver syndrome, chr5_176566162_y_119 119 NSD1 NM_172349 INTRON OMIM: 606681 NSD1, ARA267, STO Nuclear receptor binding SET domain protein 1 fusion gene with NUP98 in AML Sotos syndrome, 117550 (3); Leukemia, acute myeloid, 601626 (1);Weaver syndrome, chr6_129920941_r_119 119 ARHGAP18 NM_033515 INTRON chr6_131980592_y_119 119 ENPP3 NM_005021 INTRON OMIM: 602182 ENPP3, PDNP3 Ectonucleotide pyrophosphatase/phosphodiesterase 3 chr7_13680638_r_119 119 ETV1 NM_004956 INTRON OMIM: 600541 ETV1 ETS variant gene-1 fused with EWS in some Ewing sarcoma chr7_150861994_r_119 119 PRKAG2 NM_016203 INTRON OMIM: 602743 PRKAG2, WPWS Protein kinase, AMP-activated, noncatalytic, gamma-2 Wolff-Parkinson-White syndrome, 194200 (3); Cardiomyopathy,hypertrophic, with WP chr7_155995745_r_119 119 C7orf2 NM_022458 INTRON OMIM: 607929 C7orf22, CCM2 Malcavernin Cerebral cavernous malformations-2, 603284 (3) chr7_90136704_y_119 119 PFTK1 NM_012395 INTRON chr7_91757337_r_119 119 PEX1 NM_000466 INTRON OMIM: 602859 PEX10, NALD Peroxisome biogenesis factor 10 Zellweger syndrome, 214100 (3); Adrenoleukodystrophy, neonatal,202370 (3) chr8_105418914_r_119 119 DPYS NM_001385 INTRON OMIM: 608383 DPYSL5, CRMP5, CRAM Dihydropyrimidinase-like 5 MOUSE: 5(Dpysl5) chr9_28216611_r_119 119 FLJ31810 NM_152570 UTR chr9_34209671_y_119 119 UBAP1 NM_016525 UTR chrX_90517558_r_119 119 PCDH11X NM_032968 INTRON OMIM: 300246 PCDH11X, PCDH11, PCD Protocadherin 11, X-linked chrX_90517558_r_119 119 PCDH11X NM_032969 INTRON OMIM: 300246 PCDH11X, PCDH11, PCD Protocadherin 11, X-linked chr10_22203742_r_120 120 DNAJC1 NM_022365 INTRON chr11_47668832_r_120 120 FLJ23598 NM_024783 INTRON chr12_10232330_r_120 120 FLJ31166 NM_153022 INTRON chr12_98035587_y_120 120 EB-1 NM_152788 UTR chr12_98035587_y_120 120 EB-1 NM_020140 INTRON chr18_8326587_r_120 120 PTPRM NM_002845 INTRON OMIM: 176888 PTPRM, PTPRL1, RPTPM Protein tyrosine phosphatase, receptor type, mu polypeptide chr19_40524751_y_120 120 CD22 NM_001771 INTRON OMIM: 605397 DNAM1, CD226 DNAX accessory molecule 1 chr1_75332593_r_120 120 MGC34032 NM_152697 INTRON chr20_24476107_y_120 120 C20orf39 NM_024893 UTR chr21_40975071_r_120 120 DSCAM NM_001389 INTRON OMIM: 602523 DSCAM Down syndrome cell adhesion molecule chr22_28371060_y_120 120 NF2 NM_181825 INTRON OMIM: 606131 RNF28, SMRZ RING finger protein-28 chr22_28371060_y_120 120 NF2 NM_181831 INTRON OMIM: 606131 RNF28, SMRZ RING finger protein-28 chr22_28371060_y_120 120 NF2 NM_000268 INTRON OMIM: 606131 RNF28, SMRZ RING finger protein-28 chr22_28371060_y_120 120 NF2 NM_016418 INTRON OMIM: 606131 RNF28, SMRZ RING finger protein-28 chr22_28371060_y_120 120 NF2 NM_181826 UTR OMIM: 606131 RNF28, SMRZ RING finger protein-28 chr22_28371060_y_120 120 NF2 NM_181827 UTR OMIM: 606131 RNF28, SMRZ RING finger protein-28 chr22_28371060_y_120 120 NF2 NM_181828 INTRON OMIM: 606131 RNF28, SMRZ RING finger protein-28 chr22_28371060_y_120 120 NF2 NM_181829 INTRON OMIM: 606131 RNF28, SMRZ RING finger protein-28 chr22_28371060_y_120 120 NF2 NM_181830 INTRON OMIM: 606131 RNF28, SMRZ RING finger protein-28 chr22_28371060_y_120 120 NF2 NM_181832 INTRON OMIM: 606131 RNF28, SMRZ RING finger protein-28 chr22_28371060_y_120 120 NF2 NM_181833 INTRON OMIM: 606131 RNF28, SMRZ RING finger protein-28 chr22_28371060_y_120 120 NF2 NM_181834 INTRON OMIM: 606131 RNF28, SMRZ RING finger protein-28 chr22_28371060_y_120 120 NF2 NM_181835 INTRON OMIM: 606131 RNF28, SMRZ RING finger protein-28 chr2_73170368_y_120 120 SFXN5 NM_144579 INTRON chr3_186561285_r_120 120 LIPH NM_139248 INTRON OMIM: 607365 LIPH Lipase H chr3_49918924_r_120 120 MGC13272 NM_032355 UTR chr3_7567080_y_120 120 GRM7 NM_181875 INTRON OMIM: 604101 GRM7, MGLUR7 Glutamate receptor, metabotropic, 7 chr3_7567080_y_120 120 GRM7 NM_000844 INTRON OMIM: 604101 GRM7, MGLUR7 Glutamate receptor, metabotropic, 7 chr3_7567080_y_120 120 GRM7 NM_181874 INTRON OMIM: 604101 GRM7, MGLUR7 Glutamate receptor, metabotropic, 7 chr6_38502224_r_120 120 BTBD9 NM_152733 INTRON chr7_14481614_r_120 120 DGKB NM_004080 INTRON OMIM: 604070 DGKB, DGK Diacylglycerol kinase, beta, 90kD chr7_14481614_r_120 120 DGKB NM_145695 INTRON OMIM: 604070 DGKB, DGK Diacylglycerol kinase, beta, 90kD chr7_47169360_r_120 120 TEM6 NM_022748 INTRON OMIM: 606825 TEM6 Tumor endothelial marker 6 chr7_81426828_r_120 120 CACNA2D1 NM_000722 INTRON chr9_96061474_r_120 120 NAP1 NM_016481 INTRON OMIM: 604891 NCKAP1, NAP1 NCK-associated protein 1 chrX_527738_y_120 120 SHOX NM_006883 UTR OMIM: 602504 SHOX2, SHOT, OG12 Short stature homeo box 2 MOUSE: 3(Og12) chrX_527738_y_120 120 SHOX NM_000451 UTR OMIM: 602504 SHOX2, SHOT, OG12 Short stature homeo box 2 MOUSE: 3(Og12) chrX_68550810_y_120 120 DLG3 NM_021120 INTRON OMIM: 601114 MPP3, DLG3 Membrane protein, palmitoylated-3 (MAGUK p55 subfamily member 3) chrY_527738_y_120 120 SHOX NM_006883 UTR OMIM: 602504 SHOX2, SHOT, OG12 Short stature homeo box 2 MOUSE: 3(Og12) chrY_527738_y_120 120 SHOX NM_000451 UTR OMIM: 602504 SHOX2, SHOT, OG12 Short stature homeo box 2 MOUSE: 3(Og12) chr11_125853786_y_121 121 NEPH2 NM_032531 INTRON OMIM: 607761 NEPH2, KIAA1867, KIR Nephrin-like 2 chr11_3017512_y_121 121 CARS NM_001751 INTRON OMIM: 123859 CARS Cysteinyl-tRNA synthetase chr11_3017512_y_121 121 CARS NM_139273 INTRON OMIM: 123859 CARS Cysteinyl-tRNA synthetase chr12_106688732_y_121 121 PRDM4 NM_012406 UTR OMIM: 605780 PRDM4, PFM1 PR domain-containing protein 4 chr12_38333562_y_121 121 FLJ40126 NM_173599 INTRON chr12_7443292_y_121 121 M160 NM_174941 INTRON OMIM: 605975 SRRM1, SRM160 Serine/arginine repetitive matrix 1 (ser/arg-related nuclear matrixprotein, 160k chr13_95684172_r_121 121 MBNL2 NM_005757 INTRON chr13_95684172_r_121 121 MBNL2 NM_144778 INTRON chr14_21857246_y_121 121 MYH6 NM_002471 INTRON OMIM: 160710 MYH6 Myosin, heavy polypeptide-6, cardiac muscle, alpha Cardiomyopathy, familial hypertrophic, 192600 (3) MOUSE: 14(Myhca) chr16_22093705_r_121 121 FLJ40941 NM_173615 INTRON chr16_24091324_y_121 121 PRKCB1 NM_002738 INTRON OMIM: 176970 PRKCB1, PKCB Protein kinase C, beta 1 polypeptide chr17_60962533_r_121 121 FLJ25818 NM_173503 INTRON chr17_777662_r_121 121 CGI-150 NM_016080 UTR chr17_777662_r_121 121 NXN NM_022463 INTRON chr18_61665537_y_121 121 CDH7 NM_033646 INTRON OMIM: 602988 PCDH7, BHPCDH Protocadherin-7 chr18_61665537_y_121 121 CDH7 NM_004361 INTRON OMIM: 602988 PCDH7, BHPCDH Protocadherin-7 chr19_40230734_r_121 121 HPN NM_002151 INTRON OMIM: 142440 HPN Hepsin chr1_231524015_y_121 121 FLJ37712 NM_173508 INTRON chr20_43872702_y_121 121 PKIG NM_007066 UTR OMIM: 604932 PKIG Protein kinase, cAMP-dependent catalytic, inhibitor gamma chr20_43872702_y_121 121 PKIG NM_181804 UTR OMIM: 604932 PKIG Protein kinase, cAMP-dependent catalytic, inhibitor gamma chr20_43872702_y_121 121 PKIG NM_181805 UTR OMIM: 604932 PKIG Protein kinase, cAMP-dependent catalytic, inhibitor gamma chr20_52484050_y_121 121 FLJ33887 NM_173485 INTRON chr2_11700815_y_121 121 GREB1 NM_014668 UTR chr2_125343058_r_121 121 caspr5 NM_130773 INTRON chr2_125343058_r_121 121 caspr5 NM_138996 INTRON chr2_32432730_r_121 121 CARD12 NM_021209 INTRON OMIM: 606831 CARD12, CLAN, IPAF Caspase recruitment domain-containing protein 12 chr3_136222924_y_121 121 EPHB1 NM_004441 INTRON OMIM: 600600 EPHB1, EPHT2, NET eph tyrosine kinase 2 (ephrin receptor EphB1) chr3_143402421_y_121 121 SEP1 NM_019001 INTRON OMIM: 154030 NSEP1, YB1, DBPB Nuclease-sensitive element-binding protein 1(major histocompatibility complex, c chr3_193606436_y_121 121 FGF12 NM_004113 INTRON OMIM: 601513 FGF12, FHF1 Fibroblast growth factor-12 MOUSE: 16(Fhf1) chr4_177517315_r_121 121 GPM6A NM_005277 UTR OMIM: 601275 GPM6A, M6A Glycoprotein M6A chr4_74490059_r_121 121 GTAR NM_032217 INTRON chr5_149328961_r_121 121 PDE6A NM_000440 INTRON OMIM: 180071 PDE6A, PDEA Phosphodiesterase-6A, cGMP-specific, rod, alpha Retinitis pigmentosa, autosomal recessive (3) MOUSE: 18(Pde6a) chr7_10831825_r_121 121 KIAA0783 NM_014660 INTRON chr7_115910978_r_121 121 MET NM_000245 INTRON OMIM: 601916 ARMET, ARP Arginine-rich protein, mutated in early stage tumors Pancreatic cancer, 260350 (3) chr7_1230162_r_121 121 FLJ23471 NM_024723 INTRON chr7_99635908_y_121 121 FLJ10057 NM_017984 UTR chr8_13273728_y_121 121 DLC1 NM_182643 INTRON OMIM: 604050 DLEC1, DLC1 Deleted in lung and esophageal cancer 1 Lung cancer, 211980 (1); Esophageal cancer, 133239 (1) chr8_13273728_y_121 121 DLC1 NM_024767 INTRON OMIM: 604050 DLEC1, DLC1 Deleted in lung and esophageal cancer 1 Lung cancer, 211980 (1); Esophageal cancer, 133239 (1) chr9_130913189_y_121 121 FLJ32704 NM_152572 INTRON chr9_18616868_y_121 121 ADAMTSL1 NM_139264 INTRON chr9_18616868_y_121 121 ADAMTSL1 NM_052866 INTRON chr9_18616868_y_121 121 ADAMTSL1 NM_139238 INTRON chrX_1113255_y_121 121 IL3RA NM_002183 INTRON OMIM: 308385 IL3RA Interleukin-3 receptor, alpha subunit same 190kb segment as CSF2RA MOUSE: 14(Il3ra) chrY_1113255_y_121 121 IL3RA NM_002183 INTRON OMIM: 308385 IL3RA Interleukin-3 receptor, alpha subunit same 190kb segment as CSF2RA MOUSE: 14(Il3ra) chr10_100543352_r_122 122 HPSE2 NM_021828 INTRON chr10_102853826_y_122 122 BTRC NM_003939 INTRON OMIM: 605651 FBXW1B, BTRC2, BTRCP F-box and WD40 domain protein 1B chr10_102853826_y_122 122 BTRC NM_033637 INTRON OMIM: 605651 FBXW1B, BTRC2, BTRCP F-box and WD40 domain protein 1B chr10_53061304_y_122 122 PRKG1 NM_006258 INTRON OMIM: 176894 PRKG1, PRKG1B, PRKGR Protein kinase, cGMP-dependent, regulatory, type I chr11_119755473_y_122 122 ARHGEF12 NM_015313 INTRON OMIM: 604763 ARHGEF12, LARG, KIAA Rho guanine nucleotide exchange factor 12, leukemia-associated fused with MLL in AML Leukemia, acute myeloid (3) chr12_11713558_y_122 122 ETV6 NM_001987 INTRON OMIM: 600618 ETV6, TEL ETS variant gene-6 (TEL oncogene) fused to PDGFRB or AML1 in leukemia Leukemia, acute lymphoblastic (1) chr13_93501792_r_122 122 ABCC4 NM_005845 INTRON OMIM: 605250 ABCC4, MRP4, MOATB ATP-binding cassette, subfamily C, member 4 chr15_50240352_r_122 122 MYO5C NM_018728 INTRON chr15_65377616_r_122 122 FLJ12476 NM_022784 UTR chr15_68967646_r_122 122 FLJ20156 NM_017691 INTRON chr16_49489188_r_122 122 OAZ NM_015069 INTRON OMIM: 601579 OAZ1 Ornithine decarboxylase antizyme 1 chr17_50373020_y_122 122 CA10 NM_020178 INTRON OMIM: 604642 CA10, CARPX Carbonic anhydrase X chr18_61646857_y_122 122 CDH7 NM_033646 INTRON OMIM: 602988 PCDH7, BHPCDH Protocadherin-7 chr18_61646857_y_122 122 CDH7 NM_004361 INTRON OMIM: 602988 PCDH7, BHPCDH Protocadherin-7 chr1_204770741_y_122 122 CR1 NM_000573 INTRON OMIM: 605860 DSCR1L2, MCIP3 Down syndrome critical region gene 1-like 2 (myocyte-enrichedcalcineurin-interac MOUSE: 4(Dscr1l2) chr1_204770741_y_122 122 CR1 NM_000651 INTRON OMIM: 605860 DSCR1L2, MCIP3 Down syndrome critical region gene 1-like 2 (myocyte-enrichedcalcineurin-interac MOUSE: 4(Dscr1l2) chr1_51680358_r_122 122 NRD1 NM_002525 INTRON OMIM: 602651 NRD1 Nardilysin (N-arginine dibasic convertase) chr1_67177089_r_122 122 IL12RB2 NM_001559 INTRON OMIM: 601642 IL12RB2 Interleukin 12 receptor, beta-2 chr3_122674930_y_122 122 HCLS1 NM_005335 INTRON OMIM: 601306 HCLS1 Hematopoietic cell-specific Lyn substrate 1 chr3_178108438_r_122 122 IRA1 NM_024665 UTR chr4_101861392_y_122 122 EMCN NM_016242 INTRON chr4_123231353_r_122 122 BBS7 NM_176824 INTRON OMIM: 607590 BBS7 BBS7 gene Bardet-Biedl syndrome, 209900 (3) chr4_123231353_r_122 122 BBS7 NM_018190 INTRON OMIM: 607590 BBS7 BBS7 gene Bardet-Biedl syndrome, 209900 (3) chr4_123960982_r_122 122 IL21 NM_021803 UTR OMIM: 605384 IL21 Interleukin 21 chr4_163645441_y_122 122 DKFZp566D234 NM_020116 UTR chr4_76979505_r_122 122 CDKL2 NM_003948 INTRON chr5_19755231_r_122 122 CDH18 NM_004934 INTRON OMIM: 608287 PCDH18, KIAA1562 Protocadherin 18 chr5_53615371_r_122 122 FLJ20051 NM_019087 INTRON chr6_163600252_r_122 122 PACRG NM_152410 INTRON chr6_2806480_y_122 122 MGC39372 NM_182544 UTR chr6_39360681_y_122 122 C6orf102 NM_145027 INTRON chr6_46822303_r_122 122 MEP1A NM_005588 INTRON OMIM: 600388 MEP1A Meprin A, alpha MOUSE: 17(Mep1a) chr7_139143049_r_122 122 FLJ22693 NM_022750 INTRON chr9_33143945_r_122 122 B4GALT1 NM_001497 INTRON OMIM: 137060 B4GALT1, GGTB2, GT1, Glycoprotein-4-beta-galactosyltransferase-2 (EC 2.4.1.22) Congenital disorder of glycosylation, type IId, 607091 (3) MOUSE: 4(Ggtb) chr10_12669199_y_123 123 CKLiK NM_153498 INTRON chr10_12669199_y_123 123 CKLiK NM_020397 INTRON chr10_20337147_y_123 123 TEM7R NM_032812 INTRON OMIM: 606827 TEM7R Tumor endothelial marker 7-related protein chr11_112420284_y_123 123 NCAM1 NM_000615 INTRON OMIM: 116930 NCAM1 Neural cell adhesion molecule 1 defective in "staggerer" in mice MOUSE: 9(Ncam) chr11_16335507_r_123 123 SOX6 NM_033326 UTR OMIM: 607257 SOX6 SRY-box 6 MOUSE: 7(Sox6) chr12_26610628_r_123 123 ITPR2 NM_002223 INTRON OMIM: 600144 ITPR2 Inositol 1,4,5-triphosphate receptor, type 2 chr13_98772285_y_123 123 PCCA NM_000282 INTRON OMIM: 232000 PCCA Propionyl Coenzyme A carboxylase, alpha polypeptide Propionicacidemia, 606054 (3) MOUSE: 14(Pcca) chr17_9734869_r_123 123 LOC146845 NM_145054 INTRON chr19_16887638_y_123 123 VIP NM_015692 INTRON OMIM: 192321 VIPR1 Vasoactive intestinal peptide receptor 1 incorrectly assigned to 2q37 MOUSE: 9(Vipr1) chr19_49998669_r_123 123 RELB NM_006509 UTR chr19_7102142_y_123 123 INSR NM_000208 INTRON OMIM: 147671 INSRR, IRR Insulin receptor-related receptor chr1_177867899_y_123 123 XPR1 NM_004736 INTRON OMIM: 605237 XPR1, SYG1 Xenotropic and polytropic retrovirus receptor MOUSE: 1(Xpr1) chr1_228970572_y_123 123 DISC1 NM_018662 INTRON OMIM: 605210 DISC1 Disrupted in schizophrenia 1 Schizophrenia, 181500 (2) MOUSE: 8(Disc1) chr20_52386584_y_123 123 FLJ33887 NM_173485 INTRON chr2_11700475_y_123 123 GREB1 NM_014668 UTR chr3_132757607_y_123 123 CPNE4 NM_130808 INTRON chr3_134477322_r_123 123 BFSP2 NM_003571 INTRON OMIM: 603212 BFSP2, CP49, CP47 Beaded filament structural protein 2 (cytoskeletal protein, 49 kD) Cataract, juvenile-onset, 604219 (3); Cataract, congenital, 604219(3) chr3_134477322_r_123 123 MGC2848 NM_032917 UTR chr3_189347618_y_123 123 LPP NM_005578 UTR OMIM: 171800 ALPP Alkaline phosphatase, placental (Regan isozyme) MOUSE: 4(Akp2) chr3_42136226_y_123 123 OIP106 NM_014965 INTRON OMIM: 608112 OIP106, KIAA1042 OGT-interacting protein, 106kD chr3_60838633_y_123 123 FHIT NM_002012 UTR OMIM: 601153 FRA3B, FHIT Fragile histidine triad gene deleted in RCC MOUSE: 14(Fhit, Fra14A2) chr3_63419212_r_123 123 SYNPR NM_144642 INTRON chr4_152157285_y_123 123 LRBA NM_006726 INTRON chr4_163478969_r_123 123 DKFZp566D234 NM_020116 INTRON chr5_140906999_r_123 123 PCDHGA1 NM_018912 INTRON OMIM: 606288 PCDHGA1 Protocadherin-gamma, subfamily A, member 1 chr5_140906999_r_123 123 PCDHGA2 NM_018915 INTRON OMIM: 606289 PCDHGA2 Protocadherin-gamma, subfamily A, member 2 chr5_140906999_r_123 123 PCDHGA3 NM_018916 INTRON OMIM: 606290 PCDHGA3 Protocadherin-gamma, subfamily A, member 3 chr5_140906999_r_123 123 PCDHGB1 NM_018922 INTRON OMIM: 606299 PCDHGB1 Protocadherin-gamma, subfamily B, member 1 chr5_140906999_r_123 123 PCDHGA4 NM_018917 INTRON OMIM: 606291 PCDHGA4 Protocadherin-gamma, subfamily A, member 4 chr5_140906999_r_123 123 PCDHGB2 NM_018923 INTRON OMIM: 606300 PCDHGB2 Protocadherin-gamma, subfamily B, member 2 chr5_140906999_r_123 123 PCDHGA5 NM_018918 INTRON OMIM: 606292 PCDHGA5 Protocadherin-gamma, subfamily A, member 5 chr5_140906999_r_123 123 PCDHGB3 NM_018924 INTRON OMIM: 606301 PCDHGB3 Protocadherin-gamma, subfamily B, member 3 chr5_140906999_r_123 123 PCDHGA6 NM_018919 INTRON OMIM: 606293 PCDHGA6 Protocadherin-gamma, subfamily A, member 6 chr5_140906999_r_123 123 PCDHGA7 NM_018920 INTRON OMIM: 606294 PCDHGA7 Protocadherin-gamma, subfamily A, member 7 chr5_140906999_r_123 123 PCDHGB4 NM_003736 INTRON OMIM: 603058 PCDHGB4 Protocadherin-gamma, subfamily B, member 4 chr5_140906999_r_123 123 PCDHGA8 NM_032088 INTRON OMIM: 606295 PCDHGA8 Protocadherin-gamma, subfamily A, member 8 chr5_140906999_r_123 123 PCDHGB5 NM_018925 INTRON OMIM: 606302 PCDHGB5 Protocadherin-gamma, subfamily B, member 5 chr5_140906999_r_123 123 PCDHGA9 NM_018921 INTRON OMIM: 606296 PCDHGA9 Protocadherin-gamma, subfamily A, member 9 chr5_140906999_r_123 123 PCDHGB6 NM_018926 INTRON OMIM: 606303 PCDHGB6 Protocadherin-gamma, subfamily B, member 6 chr5_140906999_r_123 123 PCDHGA10 NM_018913 INTRON OMIM: 606297 PCDHGA10 Protocadherin-gamma, subfamily A, member 10 chr5_140906999_r_123 123 PCDHGB7 NM_018927 INTRON OMIM: 606304 PCDHGB7 Protocadherin-gamma, subfamily B, member 7 chr5_140906999_r_123 123 PCDHGA11 NM_018914 INTRON OMIM: 606298 PCDHGA11 Protocadherin-gamma, subfamily A, member 11 chr5_140906999_r_123 123 PCDHGA11 NM_032092 INTRON OMIM: 606298 PCDHGA11 Protocadherin-gamma, subfamily A, member 11 chr5_140906999_r_123 123 PCDHGA12 NM_003735 INTRON OMIM: 603059 PCDHGA12 Protocadherin-gamma, subfamily A, member 12 chr5_140906999_r_123 123 PCDHGC3 NM_002588 INTRON OMIM: 603627 PCDHGC3 Protocadherin-gamma, subfamily C, member 3 chr5_140906999_r_123 123 PCDHGC3 NM_032403 INTRON OMIM: 603627 PCDHGC3 Protocadherin-gamma, subfamily C, member 3 chr5_140906999_r_123 123 PCDHGC4 NM_018928 INTRON OMIM: 606305 PCDHGC4 Protocadherin-gamma, subfamily C, member 4 chr5_140906999_r_123 123 PCDHGC5 NM_018929 INTRON OMIM: 606306 PCDHGC5 Protocadherin-gamma, subfamily C, member 5 chr6_109237311_r_123 123 DKFZP434P0714 NM_032131 UTR chr7_115698509_r_123 123 CAV2 NM_001233 INTRON OMIM: 601048 CAV2 Caveolin-2 MOUSE: 6(Cav2) chr7_39966444_y_123 123 C7orf10 NM_024728 INTRON chr8_108302728_r_123 123 ANGPT1 NM_001146 INTRON OMIM: 601667 ANGPT1, ANG1 Angiopoietin-1 MOUSE: 15(Angpt1) chr8_108302728_r_123 123 ANGPT1 NM_139290 INTRON OMIM: 601667 ANGPT1, ANG1 Angiopoietin-1 MOUSE: 15(Angpt1) chr8_85185279_y_123 123 LOC138046 NM_173848 UTR chr9_3260049_r_123 123 RFX3 NM_134428 INTRON chr9_3260049_r_123 123 RFX3 NM_002919 INTRON chrX_131501196_y_123 123 GPC3 NM_004484 INTRON OMIM: 300037 GPC3, SDYS, SGBS1 Glypican 3 Simpson-Golabi-Behmel syndrome, type 1, 312870 (3); Wilms tumor,somatic, 194070 chrX_84626256_y_123 123 DACH2 NM_053281 INTRON chr10_102896562_y_124 124 BTRC NM_003939 INTRON OMIM: 605651 FBXW1B, BTRC2, BTRCP F-box and WD40 domain protein 1B chr10_102896562_y_124 124 BTRC NM_033637 INTRON OMIM: 605651 FBXW1B, BTRC2, BTRCP F-box and WD40 domain protein 1B chr10_20337022_y_124 124 TEM7R NM_032812 INTRON OMIM: 606827 TEM7R Tumor endothelial marker 7-related protein chr10_25173842_y_124 124 HHGP NM_020200 INTRON chr11_118672738_y_124 124 CBL NM_005188 INTRON OMIM: 604491 CBLB CAS-BR-M murine ecotropic retroviral transforming sequence B chr14_69999399_y_124 124 KIAA0440 NM_015556 UTR chr15_58357984_r_124 124 ANXA2 NM_004039 INTRON OMIM: 151740 ANXA2, ANX2L4, LPC2D Annexin A2 (lipocortin I) pseudogenes ANX2P1 on 4q21-q31; ANX2P2 on 9p13; ANX2P3 on 10q24-q22 chr16_1559418_y_124 124 KIAA0590 NM_014714 INTRON chr16_22796636_y_124 124 HS3ST2 NM_006043 INTRON OMIM: 604056 HS3ST2, 30ST2 Heparan sulfate D-glucosaminyl 3-0-sulfotransferase 2 MOUSE: 7(30st2) chr16_69085058_y_124 124 SNTB2 NM_006750 INTRON OMIM: 600027 SNTB2, SNT2B2, SNTL Syntrophin, beta-2 MOUSE: 8(Sntb2) chr16_69085058_y_124 124 SNTB2 NM_130845 UTR OMIM: 600027 SNTB2, SNT2B2, SNTL Syntrophin, beta-2 MOUSE: 8(Sntb2) chr17_41099849_y_124 124 HUMGT198A NM_016556 INTRON chr17_41099849_y_124 124 HUMGT198A NM_013290 INTRON chr18_48423099_r_124 124 DCC NM_005215 INTRON OMIM: 608378 SDCCAG1 Serologically defined colon cancer antigen 1 chr19_47301983_y_124 124 POU2F2 NM_002698 INTRON OMIM: 164176 POU2F2, OTF2, OCT2 POU domain, class 2, transcription factor 2 MOUSE: 7(Otf2) chr1_193949886_y_124 124 HF1 NM_000186 INTRON OMIM: 134370 HF1, CFH, HUS H factor-1 (complement factor H) Factor H deficiency (1); Membroproliferative glomerulonephritis (1);Hemolytic-ur MOUSE: 1(Cfh) chr1_198991794_r_124 124 NAV1 NM_020443 INTRON chr1_234442313_y_124 124 RYR2 NM_001035 INTRON OMIM: 180902 RYR2, VTSIP Ryanodine receptor-2 (cardiac) Ventricular tachycardia, stress-induced polymorphic, 604772 (3);Arrhythmogenic r MOUSE: 13(Ryr2) chr1_67063540_y_124 124 IL23R NM_144701 INTRON OMIM: 607562 IL23R Interleukin 23 receptor chr21_29990621_y_124 124 GRIK1 NM_175611 INTRON OMIM: 138245 GRIK1, GLUR5 Glutamate receptor, ionotropic, kainate 1 MOUSE: 16(Glur5) chr21_29990621_y_124 124 GRIK1 NM_000830 INTRON OMIM: 138245 GRIK1, GLUR5 Glutamate receptor, ionotropic, kainate 1 MOUSE: 16(Glur5) chr22_16613706_y_124 124 BID NM_001196 UTR OMIM: 601671 REQ, UBID4 Requiem, apoptosis response zinc finger gene MOUSE: 6(Req) chr22_17574622_r_124 124 CLTCL1 NM_001835 INTRON OMIM: 601273 CLTCL1, CLTD Clathrin, heavy polypeptide-like 1 MOUSE: 11(Cltd) chr22_17574622_r_124 124 CLTCL1 NM_007098 INTRON OMIM: 601273 CLTCL1, CLTD Clathrin, heavy polypeptide-like 1 MOUSE: 11(Cltd) chr2_111795704_r_124 124 FLJ11042 NM_018308 INTRON chr2_1268618_y_124 124 SNTG2 NM_018968 INTRON chr2_144122116_y_124 124 ARHGAP15 NM_018460 UTR chr2_223768764_r_124 124 DGAT2L1 NM_058165 INTRON chr2_85510058_y_124 124 TCF7L1 NM_031283 INTRON chr3_137880222_y_124 124 MGC3295 NM_025246 UTR chr3_187338431_y_124 124 DGKG NM_001346 INTRON OMIM: 601854 DGKG, DAGK3 Diacylglycerol kinase, gamma, 90-kD chr3_193285682_r_124 124 FGF12 NM_021032 INTRON OMIM: 601513 FGF12, FHF1 Fibroblast growth factor-12 MOUSE: 16(Fhf1) chr3_193285682_r_124 124 FGF12 NM_004113 INTRON OMIM: 601513 FGF12, FHF1 Fibroblast growth factor-12 MOUSE: 16(Fhf1) chr3_37167873_r_124 124 LRRFIP2 NM_017724 UTR chr3_37167873_r_124 124 LRRFIP2 NM_006309 UTR chr3_49919772_r_124 124 MGC13272 NM_032355 UTR chr4_62739035_r_124 124 LPHN3 NM_015236 INTRON chr5_22354464_r_124 124 CDH12 NM_004061 UTR OMIM: 600562 CDH12, CDHB Cadherin-12 (N-cadherin 2) pseudogene on 5q13 in SMA region chr6_102255477_y_124 124 GRIK2 NM_021956 INTRON OMIM: 138244 GRIK2, GLUR6 Glutamate receptor, ionotropic, kainate 2 chr6_102255477_y_124 124 GRIK2 NM_175768 INTRON OMIM: 138244 GRIK2, GLUR6 Glutamate receptor, ionotropic, kainate 2 chr6_154811169_r_124 124 FLJ31349 NM_173515 INTRON chr6_1941285_y_124 124 GMDS NM_001500 INTRON OMIM: 602884 GMDS GDP-mannose 4,6-dehydratase chr7_147224795_r_124 124 CNTNAP2 NM_014141 INTRON OMIM: 604569 CNTNAP2, CASPR2, NRX Contactin-associated protein-like 2 chr8_126285517_y_124 124 FLJ32440 NM_173685 INTRON chr9_37178784_y_124 124 FLJ22611 NM_032226 INTRON chrX_131631411_y_124 124 GPC3 NM_004484 INTRON OMIM: 300037 GPC3, SDYS, SGBS1 Glypican 3 Simpson-Golabi-Behmel syndrome, type 1, 312870 (3); Wilms tumor,somatic, 194070 chr10_25291203_y_125 125 MGC26778 NM_145010 INTRON chr14_88342060_r_125 125 C14orf143 NM_145231 INTRON chr15_55159126_y_125 125 TCF12 NM_003205 INTRON OMIM: 600480 TCF12, HTF4 Transcription factor-12 (HTF4, helix-loop-helix transcriptionfactors-4) chr15_72874109_r_125 125 SCAMP2 NM_005697 INTRON OMIM: 606912 SCAMP2 Secretory carrier membrane protein 2 chr15_88131442_r_125 125 AP3S2 NM_005829 INTRON chr16_3889964_r_125 125 CREBBP NM_004380 INTRON OMIM: 600140 CREBBP, CBP, RSTS CREB binding protein fusion partner with MORF in AML; fusion partner with MLL intherapy-related acute Rubenstein-Taybi syndrome, 180849 (3) chr16_7279296_r_125 125 A2BP1 NM_018723 INTRON chr16_74972728_y_125 125 ZFP1 NM_153688 UTR OMIM: 602507 ZFP103, KF1 Zinc finger protein 103, mouse, homolog of chr16_78078319_y_125 125 WWOX NM_130791 INTRON OMIM: 605131 WWOX, FOR WW domain-containing oxidoreductase Esophageal squamous cell carcinoma, 133239 (3) MOUSE: 8(Wox1, Fra8E1) chr16_78078319_y_125 125 WWOX NM_018560 INTRON OMIM: 605131 WWOX, FOR WW domain-containing oxidoreductase Esophageal squamous cell carcinoma, 133239 (3) MOUSE: 8(Wox1, Fra8E1) chr16_78078319_y_125 125 WWOX NM_016373 INTRON OMIM: 605131 WWOX, FOR WW domain-containing oxidoreductase Esophageal squamous cell carcinoma, 133239 (3) MOUSE: 8(Wox1, Fra8E1) chr16_78078319_y_125 125 WWOX NM_130788 INTRON OMIM: 605131 WWOX, FOR WW domain-containing oxidoreductase Esophageal squamous cell carcinoma, 133239 (3) MOUSE: 8(Wox1, Fra8E1) chr16_78078319_y_125 125 WWOX NM_130790 INTRON OMIM: 605131 WWOX, FOR WW domain-containing oxidoreductase Esophageal squamous cell carcinoma, 133239 (3) MOUSE: 8(Wox1, Fra8E1) chr16_78078319_y_125 125 WWOX NM_130792 INTRON OMIM: 605131 WWOX, FOR WW domain-containing oxidoreductase Esophageal squamous cell carcinoma, 133239 (3) MOUSE: 8(Wox1, Fra8E1) chr16_83321321_r_125 125 CDH13 NM_001257 INTRON OMIM: 601364 CDH13, CDHH Cadherin-13 (H-cadherin, heart) chr18_51178547_r_125 125 TCF4 NM_003199 INTRON OMIM: 602228 TCF7L2, TCF4 Transcription factor 7-like 2 chr18_59599376_r_125 125 SERPINB7 NM_003784 INTRON chr19_44009513_r_125 125 ECH1 NM_001398 INTRON OMIM: 600696 ECH1 Enoyl Coenzyme A hydratase 1, peroxisomal chr1_54571738_r_125 125 TTC4 NM_004623 INTRON OMIM: 606753 TTC4 Tetratricopeptide repeat domain 4 pseudogene on 7p14-p13 chr20_13563872_r_125 125 C20orf13 NM_017714 INTRON chr22_35318214_y_125 125 CACNG2 NM_006078 INTRON OMIM: 602911 CACNG2 Calcium channel, voltage-dependent, gamma-2 subunit MOUSE: 15(Cacng2) chr2_11492750_r_125 125 ROCK2 NM_004850 INTRON OMIM: 604002 ROCK2 RHO-associated coiled-coil-containing protein kinase 2 chr2_120365011_y_125 125 SCTR NM_002980 INTRON OMIM: 182098 SCTR Secretin receptor chr2_159352998_y_125 125 LOC130940 NM_138803 INTRON chr2_4860001_r_125 125 TSSC1 NM_003310 INTRON chr2_50625800_r_125 125 NRXN1 NM_004801 INTRON OMIM: 600565 NRXN1 Neurexin 1 chr2_62973792_r_125 125 KIAA0903 NM_015252 INTRON chr4_185730903_y_125 125 MGC33971 NM_153343 INTRON chr4_21283779_y_125 125 KCNIP4 NM_147182 UTR OMIM: 608182 KCNIP4, KCHIP4 Kv channel-interacting protein 4 chr5_14812607_r_125 125 ANKH NM_019847 INTRON OMIM: 605145 ANKH, HANK, ANK, CMD Ank, mouse, homolog of Craniometaphyseal dysplasia, 123000 (3); Chondrocalcinosis 2,118600 (3) MOUSE: 15(ank) chr5_14812607_r_125 125 ANKH NM_054027 INTRON OMIM: 605145 ANKH, HANK, ANK, CMD Ank, mouse, homolog of Craniometaphyseal dysplasia, 123000 (3); Chondrocalcinosis 2,118600 (3) MOUSE: 15(ank) chr7_100003891_r_125 125 ZAN NM_003386 INTRON OMIM: 602372 ZAN Zonadhesin MOUSE: 5(Zan) chr7_100003891_r_125 125 ZAN NM_173055 UTR OMIM: 602372 ZAN Zonadhesin MOUSE: 5(Zan) chr7_100003891_r_125 125 ZAN NM_173056 UTR OMIM: 602372 ZAN Zonadhesin MOUSE: 5(Zan) chr7_100003891_r_125 125 ZAN NM_173057 UTR OMIM: 602372 ZAN Zonadhesin MOUSE: 5(Zan) chr7_100003891_r_125 125 ZAN NM_173058 UTR OMIM: 602372 ZAN Zonadhesin MOUSE: 5(Zan) chr7_100003891_r_125 125 ZAN NM_173059 INTRON OMIM: 602372 ZAN Zonadhesin MOUSE: 5(Zan) chr7_100339833_r_125 125 SERPINE1 NM_000602 INTRON chr7_131663576_y_125 125 DKFZp434G0625 NM_181775 UTR chr7_145674532_r_125 125 CNTNAP2 NM_014141 INTRON OMIM: 604569 CNTNAP2, CASPR2, NRX Contactin-associated protein-like 2 chr7_70062043_y_125 125 WBSCR17 NM_022479 INTRON chr8_141728768_r_125 125 PTK2 NM_005607 INTRON OMIM: 601212 PTK2B, FAK2, PYK2 Protein tyrosine kinase-2, beta (focal adhesion kinase 2) chr8_141728768_r_125 125 PTK2 NM_153831 INTRON OMIM: 601212 PTK2B, FAK2, PYK2 Protein tyrosine kinase-2, beta (focal adhesion kinase 2) chr8_40663841_r_125 125 FLJ13842 NM_024645 INTRON chr9_70827048_r_125 125 TMC1 NM_138691 INTRON OMIM: 606706 TMC1, DFNB7, DFNB11, Transmembrane cochlear-expressed gene 1 Deafness, autosomal recessive 7, 600974 (3); Deafness, autosomaldominant 36, 606 MOUSE: 19(Tmc1, dn, Bth) chr9_70980542_r_125 125 ALDH1A1 NM_000689 INTRON OMIM: 100640 ALDH1A1 Aldehyde dehydrogenase-1 family, member A1, soluble MOUSE: 19(Ahd2) chrX_5357811_y_125 125 NLGN4 NM_020742 INTRON OMIM: 300427 NLGN4, KIAA1260 Neuroligin 4 Autism, X-linked, 300425 (3); Asperger syndrome, 300425 (3) chrX_5357811_y_125 125 NLGN4 NM_181332 INTRON OMIM: 300427 NLGN4, KIAA1260 Neuroligin 4 Autism, X-linked, 300425 (3); Asperger syndrome, 300425 (3) chrX_99869122_y_125 125 NXF5 NM_032946 INTRON OMIM: 300319 NXF5 Nuclear RNA export factor 5 chrX_99869122_y_125 125 NXF5 NM_033152 INTRON OMIM: 300319 NXF5 Nuclear RNA export factor 5 chrX_99869122_y_125 125 NXF5 NM_033153 INTRON OMIM: 300319 NXF5 Nuclear RNA export factor 5 chrX_99869122_y_125 125 NXF5 NM_033154 INTRON OMIM: 300319 NXF5 Nuclear RNA export factor 5 chrX_99869122_y_125 125 NXF5 NM_033155 INTRON OMIM: 300319 NXF5 Nuclear RNA export factor 5 chr10_70559868_y_126 126 NET-7 NM_012339 INTRON chr10_72531515_r_126 126 CDH23 NM_052836 UTR OMIM: 605516 CDH23, USH1D Cadherin-23 (otocadherin) between D10S529 and D10S573 Usher syndrome, type 1D, 601067 (3); Deafness, autosomal recessive12, 601386 (3) MOUSE: 10(Cdh23, v) chr10_72531515_r_126 126 CDH23 NM_022124 UTR OMIM: 605516 CDH23, USH1D Cadherin-23 (otocadherin) between D10S529 and D10S573 Usher syndrome, type 1D, 601067 (3); Deafness, autosomal recessive12, 601386 (3) MOUSE: 10(Cdh23, v) chr12_118700173_r_126 126 CIT NM_007174 INTRON OMIM: 606815 CITED4 CBP/P300-interacting transactivator, with glu/asp-rich carboxyterminal domain, 4 chr12_81658108_y_126 126 DKFZp762A217 NM_152588 INTRON chr13_65183846_y_126 126 PCDH9 NM_020403 INTRON OMIM: 603581 PCDH9 Protocadherin 9 MOUSE: 14(Pcdh9) chr16_64876729_r_126 126 CDH11 NM_001797 UTR OMIM: 600023 CDH11, CAD11 Cadherin-11 (OB-cadherin, osteoblast) MOUSE: 8(cad11) chr16_64876729_r_126 126 CDH11 NM_033664 UTR OMIM: 600023 CDH11, CAD11 Cadherin-11 (OB-cadherin, osteoblast) MOUSE: 8(cad11) chr17_81274881_r_126 126 LOC56270 NM_019613 UTR chr18_65739345_r_126 126 DNAM-1 NM_006566 INTRON chr18_9476189_y_126 126 RALBP1 NM_006788 UTR OMIM: 605801 RALBP1, RLIP76 RALA-binding protein 1 chr19_13365534_y_126 126 CACNA1A NM_000068 INTRON OMIM: 601011 CACNA1A, CACNL1A4, S Calcium channel, voltage-dependent, P/Q type, alpha 1A subunit Hemiplegic migraine, familial, 141500 (3); Episodic ataxia, type 2,108500 (3); S MOUSE: 8(tg, Cacl1a4) chr19_13365534_y_126 126 CACNA1A NM_023035 INTRON OMIM: 601011 CACNA1A, CACNL1A4, S Calcium channel, voltage-dependent, P/Q type, alpha 1A subunit Hemiplegic migraine, familial, 141500 (3); Episodic ataxia, type 2,108500 (3); S MOUSE: 8(tg, Cacl1a4) chr1_143027396_y_126 126 LOC64182 NM_022359 UTR chr20_24637097_r_126 126 C20orf39 NM_024893 INTRON chr20_8807517_y_126 126 PLCB1 NM_015192 INTRON chr2_230454731_r_126 126 DNER NM_139072 INTRON OMIM: 607299 DNER Delta-and notch-like egf-related receptor chr2_31584322_r_126 126 XDH NM_000379 INTRON OMIM: 607633 XDH Xanthine dehydrogenase (xanthine oxidase) Xanthinuria, type I, 278300 (3) MOUSE: 17(Xd) chr3_136222737_y_126 126 EPHB1 NM_004441 INTRON OMIM: 600600 EPHB1, EPHT2, NET eph tyrosine kinase 2 (ephrin receptor EphB1) chr4_166952062_y_126 126 CPE NM_001873 INTRON OMIM: 114855 CPE Carboxypeptidase E MOUSE: 8(Cpe) chr4_21074249_r_126 126 KCNIP4 NM_147182 UTR OMIM: 608182 KCNIP4, KCHIP4 Kv channel-interacting protein 4 chr5_146101175_y_126 126 PPP2R2B NM_004576 INTRON OMIM: 604325 PPP2R2B Protein phosphatase 2, regulatory subunit B, beta Spinocerebellar ataxia 12, 604326 (3) chr5_146101175_y_126 126 PPP2R2B NM_181675 INTRON OMIM: 604325 PPP2R2B Protein phosphatase 2, regulatory subunit B, beta Spinocerebellar ataxia 12, 604326 (3) chr5_146101175_y_126 126 PPP2R2B NM_181676 INTRON OMIM: 604325 PPP2R2B Protein phosphatase 2, regulatory subunit B, beta Spinocerebellar ataxia 12, 604326 (3) chr5_146101175_y_126 126 PPP2R2B NM_181674 INTRON OMIM: 604325 PPP2R2B Protein phosphatase 2, regulatory subunit B, beta Spinocerebellar ataxia 12, 604326 (3) chr5_146101175_y_126 126 PPP2R2B NM_181677 INTRON OMIM: 604325 PPP2R2B Protein phosphatase 2, regulatory subunit B, beta Spinocerebellar ataxia 12, 604326 (3) chr5_146101175_y_126 126 PPP2R2B NM_181678 INTRON OMIM: 604325 PPP2R2B Protein phosphatase 2, regulatory subunit B, beta Spinocerebellar ataxia 12, 604326 (3) chr5_169698815_r_126 126 LCP2 NM_005565 INTRON OMIM: 601603 LCP2, SLP76 Lymphocyte cytosolic protein-2 (SH2 domain-containing leukocyteprotein of 76kD) chr6_36296653_r_126 126 PNPLA1 NM_173676 UTR chr6_43056203_r_126 126 KIAA0076 NM_014780 INTRON chr7_115698382_r_126 126 CAV2 NM_001233 INTRON OMIM: 601048 CAV2 Caveolin-2 MOUSE: 6(Cav2) chr7_139091842_r_126 126 TBXAS1 NM_001061 INTRON OMIM: 274180 TBXAS1 Thromboxane A synthase 1, platelet Thromboxane synthase deficiency (2) MOUSE: 6(Tbxas1) chr7_139091842_r_126 126 TBXAS1 NM_030984 INTRON OMIM: 274180 TBXAS1 Thromboxane A synthase 1, platelet Thromboxane synthase deficiency (2) MOUSE: 6(Tbxas1) chr7_2697076_r_126 126 CARD11 NM_032415 INTRON chr7_72088444_r_126 126 FKBP6 NM_003602 INTRON OMIM: 604839 FKBP6 FK506-binding protein 6 chr8_108979944_r_126 126 MGC35555 NM_178565 UTR chr9_35703704_r_126 126 TLN1 NM_006289 INTRON OMIM: 186745 TLN1 Talin 1 chr9_36914732_r_126 126 PAX5 NM_016734 INTRON OMIM: 167414 PAX5, BSAP Paired box homeotic gene-5 (B-cell lineage specific activatorprotein) Lymphoplasmacytoid lymphoma (1) MOUSE: 4(Pax5) chrX_151973971_y_126 126 CXorf2 NM_001586 INTRON chrX_27008946_y_126 126 FLJ32742 NM_152580 UTR chrX_45996241_r_126 126 RGN NM_004683 INTRON OMIM: 602350 NRGN Neurogranin MOUSE: 9(Nrgn) chrX_45996241_r_126 126 RGN NM_152869 INTRON OMIM: 602350 NRGN Neurogranin MOUSE: 9(Nrgn) chr11_101765711_y_127 127 BIRC2 NM_001166 INTRON chr11_16008160_y_127 127 SOX6 NM_033326 INTRON OMIM: 607257 SOX6 SRY-box 6 MOUSE: 7(Sox6) chr11_17882394_r_127 127 DELGEF NM_012139 INTRON OMIM: 606051 DELGEF Deafness locus-associated putative guanine nucleotide exchange factor chr11_331057_r_127 127 SIRT3 NM_012239 UTR OMIM: 604481 SIRT3, SIR2L3 Sirtuin, S. cerevisiae, homolog 3 chr12_5791717_r_127 127 C12orf3 NM_020373 INTRON chr13_75891816_y_127 127 PAM NM_015057 UTR OMIM: 170270 PAM Peptidylglycine alpha-amidating monooxygenase MOUSE: 1(Pam) chr14_30064946_y_127 127 FLJ12660 NM_025152 INTRON chr15_62024791_r_127 127 DAPK2 NM_014326 INTRON chr15_70521881_y_127 127 ARIH1 NM_005744 INTRON OMIM: 605624 ARIH1, ARI, UBCH7BP Ariadne, Drosophila, homolog of, 1 chr16_6707198_y_127 127 A2BP1 NM_018723 UTR chr16_84659443_y_127 127 DKFZP434B044 NM_031476 INTRON chr17_74569058_r_127 127 ACOX1 NM_004035 INTRON OMIM: 264470 ACOX1, ACOX Acyl-Coenzyme A oxidase 1 Adrenoleukodystrophy, pseudoneonatal (2) chr17_74569058_r_127 127 ACOX1 NM_007292 INTRON OMIM: 264470 ACOX1, ACOX Acyl-Coenzyme A oxidase 1 Adrenoleukodystrophy, pseudoneonatal (2) chr17_8144427_r_127 127 ALOX15B NM_001141 INTRON chr18_22885153_r_127 127 CHST9 NM_031422 INTRON chr18_27868505_r_127 127 RNF125 NM_017831 INTRON chr18_6352106_r_127 127 FLJ35936 NM_173464 UTR chr1_118782545_r_127 127 TBX15 NM_152380 INTRON OMIM: 604127 TBX15 T-box 15 MOUSE: 3(Tbx15) chr1_194802266_r_127 127 FLJ20054 NM_019049 INTRON chr20_4100588_y_127 127 MGC34919 NM_182582 UTR chr21_40914193_r_127 127 DSCAM NM_001389 INTRON OMIM: 602523 DSCAM Down syndrome cell adhesion molecule chr2_106306936_y_127 127 ECRG4 NM_032411 INTRON chr2_111795829_r_127 127 FLJ11042 NM_018308 INTRON chr2_128532933_y_127 127 PROC NM_000312 UTR OMIM: 176860 PROC Protein C (inactivator of coagulation factors Va and VIIIa) Thrombophilia due to protein C deficiency (3); Purpura fulminans,neonatal (1) chr3_116878950_y_127 127 LSAMP NM_002338 INTRON OMIM: 603241 LSAMP, LAMP Limbic system-associated membrane protein MOUSE: 16(Lsamp) chr3_162407944_y_127 127 ADMP NM_145035 UTR chr3_85969619_r_127 127 LOC253559 NM_153184 INTRON chr3_98578784_y_127 127 DKFZp434C1418 NM_173655 INTRON chr4_96500153_y_127 127 BMPR1B NM_001203 INTRON OMIM: 603248 BMPR1B, ALK6 Bone morphogenetic protein receptor, type IB chr5_131620227_r_127 127 P4HA2 NM_004199 INTRON chr5_167747870_y_127 127 KIBRA NM_015238 INTRON chr6_161078624_r_127 127 PLG NM_000301 INTRON OMIM: 191164 EFNA1, EPLG1, TNFAIP eph-related receptor tyrosine kinase ligand 1 (tumor necrosis factor,alpha-induc MOUSE: 3(Epl1) chr7_146034892_y_127 127 CNTNAP2 NM_014141 INTRON OMIM: 604569 CNTNAP2, CASPR2, NRX Contactin-associated protein-like 2 chr7_43268783_r_127 127 KIAA0322 NM_015052 INTRON chr7_98884613_y_127 127 CYP3A5 NM_000777 INTRON OMIM: 605325 CYP3A5, P450PCN3 Cytochrome P450, subfamily IIIA, polypeptide 5 chr8_102477895_y_127 127 FLJ13782 NM_024915 INTRON chr8_26501489_y_127 127 DPYSL2 NM_001386 INTRON OMIM: 602463 DPYSL2, DRP2, CRMP2 Dihydropyrimidinase-like 2 chr9_126064439_y_127 127 MGC46424 NM_173492 INTRON chr9_134372133_r_127 127 MGC23427 NM_144653 INTRON chrX_66403933_r_127 127 OPHN1 NM_002547 INTRON OMIM: 300127 OPHN1 Oligophrenin-1 Mental retardation, X-linked, 60 (3) chr14_77718750_r_128 128 NRXN3 NM_004796 INTRON OMIM: 600567 NRXN3 Neurexin 3 chr15_51677201_r_128 128 FLJ38736 NM_182758 INTRON chr16_57694786_y_128 128 CNGB1 NM_001297 INTRON OMIM: 600724 CNGB1, CNCG3L, CNCG2 Cyclic nucleotide gated channel, beta 1 Retinitis pigmentosa, autosomal recessive, 268000 (3) chr17_58882218_y_128 128 USP32 NM_032582 INTRON OMIM: 607740 USP32, USP10 Ubiquitin-specific protease 32 chr17_730930_r_128 128 CGI-150 NM_016080 UTR chr17_730930_r_128 128 NXN NM_022463 INTRON chr17_73328382_r_128 128 RAB37 NM_175738 INTRON chr18_6352235_r_128 128 FLJ35936 NM_173464 UTR chr19_14523677_y_128 128 GPSN2 NM_138501 INTRON chr19_14523677_y_128 128 GPSN2 NM_004868 INTRON chr19_53607440_r_128 128 GRIN2D NM_000836 INTRON OMIM: 602717 GRIN2D, NMDAR2D Glutamate receptor, ionotropic, N-methyl-D-aspartate 2D chr19_6132269_r_128 128 BGR NM_030924 INTRON OMIM: 300190 SH3BGR SH3-binding domain glutamic acid-rich protein-like chr1_212821090_y_128 128 KCTD3 NM_016121 INTRON chr1_99581100_r_128 128 PALMD NM_017734 INTRON chr3_196225297_r_128 128 FLJ35155 NM_152531 INTRON chr3_7255414_y_128 128 GRM7 NM_181875 INTRON OMIM: 604101 GRM7, MGLUR7 Glutamate receptor, metabotropic, 7 chr3_7255414_y_128 128 GRM7 NM_000844 INTRON OMIM: 604101 GRM7, MGLUR7 Glutamate receptor, metabotropic, 7 chr3_7255414_y_128 128 GRM7 NM_181874 INTRON OMIM: 604101 GRM7, MGLUR7 Glutamate receptor, metabotropic, 7 chr4_7515054_y_128 128 SORCS2 NM_020777 INTRON OMIM: 606284 SORCS2, KIAA1329 SORCS receptor 2 chr5_169790840_r_128 128 KCNMB1 NM_004137 INTRON OMIM: 603951 KCNMB1 Potassium large conductance calcium-activated channel, subfamily M,beta member 1 chr6_158821709_y_128 128 TULP4 NM_020245 INTRON chr6_167661601_y_128 128 NYD-TSPG NM_031949 INTRON chr6_69748710_r_128 128 BAI3 NM_001704 INTRON OMIM: 602684 BAI3 Brain-specific angiogenesis inhibitor-3 chr6_89902093_r_128 128 GABRR1 NM_002042 INTRON OMIM: 137161 GABRR1 Gamma-aminobutyric acid (GABA) A receptor, rho-1 MOUSE: 4(Gabbr1) chr7_14517709_r_128 128 DGKB NM_004080 INTRON OMIM: 604070 DGKB, DGK Diacylglycerol kinase, beta, 90kD chr7_14517709_r_128 128 DGKB NM_145695 INTRON OMIM: 604070 DGKB, DGK Diacylglycerol kinase, beta, 90kD chr7_18764628_y_128 128 HDAC9 NM_178423 INTRON OMIM: 606543 HDAC9, MITR, HDAC7B, Histone deacetylase 9 chr7_18764628_y_128 128 HDAC9 NM_178425 INTRON OMIM: 606543 HDAC9, MITR, HDAC7B, Histone deacetylase 9 chr8_22336432_y_128 128 PPP3CC NM_005605 INTRON OMIM: 114107 PPP3CC, CALNA3 Protein phosphatase-3 (formerly 2B), catalytic subunit, gamma isoform(calcineuri chr8_86325494_y_128 128 CA1 NM_001738 INTRON OMIM: 230000 FUCA1 Fucosidase, alpha-L- 1, tissue 8cM distal to RH; pseudogene on 2q31-q32 Fucosidosis (3) MOUSE: 4(Fuca) chr9_114770483_r_128 128 ASTN2 NM_014010 INTRON chrX_66404252_r_128 128 OPHN1 NM_002547 INTRON OMIM: 300127 OPHN1 Oligophrenin-1 Mental retardation, X-linked, 60 (3) chr11_132006848_r_129 129 OPCML NM_002545 INTRON OMIM: 600632 OPCML Opioid-binding protein/cell adhesion molecule-like ?on 11q22-q23 MOUSE: 9(Obcam) chr12_118217830_r_129 129 MGC39827 NM_178499 INTRON chr12_26973922_r_129 129 FLJ10637 NM_018164 INTRON chr14_69998999_y_129 129 KIAA0440 NM_015556 UTR chr16_24290725_r_129 129 CACNG3 NM_006539 INTRON OMIM: 606403 CACNG3 Calcium channel, voltage-dependent, gamma-3 subunit chr17_55019743_r_129 129 FLJ38335 NM_153228 INTRON chr17_550734_r_129 129 FLJ10979 NM_018289 INTRON chr18_27289469_y_129 129 DSG3 NM_001944 INTRON OMIM: 169615 DSG3 Desmoglein-3 (pemphigus vulgaris antigen) MOUSE: 18(Dsg3) chr18_40727140_r_129 129 SETBP1 NM_015559 INTRON chr18_61597956_y_129 129 CDH7 NM_033646 INTRON OMIM: 602988 PCDH7, BHPCDH Protocadherin-7 chr18_61597956_y_129 129 CDH7 NM_004361 INTRON OMIM: 602988 PCDH7, BHPCDH Protocadherin-7 chr19_12458242_r_129 129 FLJ38281 NM_152601 UTR chr19_2543725_r_129 129 FLJ00058 NM_052847 UTR chr19_54055839_r_129 129 PLEKHA4 NM_020904 INTRON OMIM: 607769 PLEKHA4, PEPP1 Pleckstrin homology domain-containing protein, family A, member 4 chr1_56593197_y_129 129 C8A NM_000562 UTR OMIM: 120950 C8A Complement component-8, alpha polypeptide C8 deficiency, type I (2) chr20_41491899_y_129 129 PTPRT NM_007050 INTRON chr20_41491899_y_129 129 PTPRT NM_133170 INTRON chr20_43937707_y_129 129 ADA NM_000022 INTRON OMIM: 604779 ADAM30 A disintegrin and metalloproteinase domain 30 chr2_55146826_y_129 129 RTN4 NM_007008 UTR OMIM: 604475 RTN4, NOGO Neurite outgrowth inhibitor (reticulon 4) chr2_80095652_y_129 129 CTNNA2 NM_004389 INTRON OMIM: 114025 CTNNA2, CAPR, CTNR Catenin, alpha-2 (cadherin-associated protein, related) MOUSE: 6(Capr) chr3_193907958_r_129 129 LOC151963 NM_178496 INTRON chr4_108363250_r_129 129 DKK2 NM_014421 INTRON chr4_30726651_y_129 129 PCDH7 NM_032457 INTRON OMIM: 602988 PCDH7, BHPCDH Protocadherin-7 chr5_175268339_r_129 129 CPLX2 NM_006650 UTR OMIM: 605033 CPLX2 Complexin 2 chr5_45448342_y_129 129 HCN1 NM_021072 INTRON chr5_93332356_r_129 129 DKFZP564D172 NM_032042 INTRON chr6_112140329_r_129 129 FYN NM_002037 UTR OMIM: 137025 FYN FYN oncogene related to SRC, FGR, YES proximal 6q21 MOUSE: 10(Fyn) chr6_76313760_r_129 129 SUSP1 NM_015571 INTRON OMIM: 605003 SUSP1 SUMO1-specific protease 1 chr7_106970944_y_129 129 SLC26A3 NM_000111 INTRON OMIM: 126650 SLC26A3, DRA, CLD Solute carrier family 26 (sulfate transporter), member 3 5' and close to PDS ?Colon cancer (1); Chloride diarrhea, congenital, Finnish type,214700 (3) chr7_120190420_y_129 129 FLJ21986 NM_024913 INTRON chr7_156216819_r_129 129 HLXB9 NM_005515 INTRON OMIM: 142994 HLXB9, HOXHB9, SCRA1 Homeo box-HB9 Currarino syndrome, 176450 (3) chr8_133642948_r_129 129 TSLRP NM_012472 INTRON chr9_35318593_y_129 129 UNC13 NM_006377 INTRON OMIM: 605836 UNC13, MUNC13 UNC13, C. elegans, homolog of chrX_98894598_r_129 129 NOX1 NM_007052 INTRON OMIM: 602100 PKNOX1 PBX/knotted 1 homeo box 1 MOUSE: 17(Pknox1) chrX_98894598_r_129 129 NOX1 NM_013954 INTRON OMIM: 602100 PKNOX1 PBX/knotted 1 homeo box 1 MOUSE: 17(Pknox1) chrX_98894598_r_129 129 NOX1 NM_013955 INTRON OMIM: 602100 PKNOX1 PBX/knotted 1 homeo box 1 MOUSE: 17(Pknox1) chr10_13925707_y_130 130 FLJ10210 NM_018027 INTRON chr11_47000051_r_130 130 MGC4707 NM_024113 INTRON chr11_619154_y_130 130 SIRT3 NM_012239 UTR OMIM: 604481 SIRT3, SIR2L3 Sirtuin, S. cerevisiae, homolog 3 chr12_63763778_y_130 130 WIF1 NM_007191 INTRON OMIM: 605186 WIF1 WNT inhibitory factor 1 chr13_108520370_r_130 130 COL4A1 NM_001845 INTRON OMIM: 120130 COL4A1 Collagen IV, alpha-1 polypeptide MOUSE: 8(Col4a1) chr14_33631650_y_130 130 KIAA0391 NM_014672 INTRON chr15_57291130_r_130 130 MYO1E NM_004998 INTRON OMIM: 601479 MYO1E, MYO1C Myosin IE MOUSE: 9(Myo1e) chr16_10226814_r_130 130 GRIN2A NM_000833 INTRON OMIM: 138253 GRIN2A, NMDAR2A Glutamate receptor, ionotropic, N-methyl D-aspartate 2A chr16_29645274_r_130 130 LAT1-3TM NM_031211 INTRON chr17_54772780_r_130 130 FLJ38335 NM_153228 INTRON chr18_59375187_y_130 130 SERPINB12 NM_080474 INTRON chr19_46597383_y_130 130 BCKDHA NM_000709 INTRON OMIM: 248600 BCKDHA, MSUD1 Branched chain keto acid dehydrogenase E1, alpha polypeptide Maple syrup urine disease, type Ia (3) chr1_159421563_y_130 130 CAPON NM_014697 INTRON OMIM: 605551 CAPON, KIAA0464 C-terminal PDZ domain ligand of neuronal nitric oxide synthase chr1_2939560_r_130 130 PRDM16 NM_022114 INTRON OMIM: 605557 PRDM16, MEL1 PR domain-containing protein 16 chr1_33969037_r_130 130 CSMD2 NM_052896 INTRON OMIM: 608398 CSMD2, KIAA1884 Cub and Sushi multiple domains 2 chr20_38210174_y_130 130 PPP1R16B NM_015568 INTRON chr20_43662468_y_130 130 R3HDML NM_178491 INTRON chr20_46855508_y_130 130 NCOA3 NM_006534 UTR OMIM: 601937 NCOA3, AIB1, TNRC14 Nuclear receptor coactivator 3 (amplified in breast cancer-1) chr20_46855508_y_130 130 NCOA3 NM_181659 UTR OMIM: 601937 NCOA3, AIB1, TNRC14 Nuclear receptor coactivator 3 (amplified in breast cancer-1) chr22_15647149_r_130 130 MGC57211 NM_175878 INTRON chr22_35717846_r_130 130 TMPRSS6 NM_153609 INTRON chr2_115536199_y_130 130 DPP10 NM_020868 INTRON chr2_182088822_y_130 130 UBE2E3 NM_006357 INTRON OMIM: 604151 UBE2E3, UBCH9 Ubiquitin-conjugating enzyme E2E 3 chr2_233145174_y_130 130 MGC42174 NM_152383 INTRON chr3_19925029_r_130 130 FLJ25200 NM_144715 INTRON chr6_87797833_r_130 130 CGA NM_000735 UTR OMIM: 118850 CGA Chorionic gonadotropin, alpha polypeptide shared with LH, FSH, TSH MOUSE: 4(Tsha) chr7_28333710_y_130 130 H_GS165L15.1 NM_004904 INTRON chr7_3105705_y_130 130 SDK1 NM_152744 INTRON chr7_73642359_r_130 130 GTF2IRD2 NM_173537 INTRON chr7_83332622_r_130 130 SEMA3A NM_006080 INTRON chr7_86772184_r_130 130 ABCB1 NM_000927 INTRON OMIM: 605454 ABCB10, MTABC2 ATP-binding cassette, subfamily B, member 10 pseudogene on 15q13-q14 chr8_104139902_r_130 130 BAALC NM_024812 INTRON OMIM: 606602 BAALC Brain and acute leukemia gene, cytoplasmic chr9_110837878_r_130 130 HSPC043 NM_021218 INTRON chr10_22639366_y_131 131 SPAG6 NM_012443 INTRON OMIM: 605730 SPAG6 Sperm-associated antigen 6 chr10_22639366_y_131 131 SPAG6 NM_172242 INTRON OMIM: 605730 SPAG6 Sperm-associated antigen 6 chr12_108088695_y_131 131 ACACB NM_001093 INTRON OMIM: 601557 ACACB, ACCB, ACC2 Acetyl-Coenzyme A carboxylase, beta chr16_19644746_y_131 131 MGC16824 NM_020314 INTRON chr17_66121981_y_131 131 PITPNC1 NM_012417 INTRON chr17_66121981_y_131 131 PITPNC1 NM_181671 INTRON chr19_37838764_r_131 131 DKFZP434L0718 NM_032139 INTRON chr19_8101468_r_131 131 FBN3 NM_032447 INTRON chr1_227922159_r_131 131 CAPN9 NM_006615 INTRON OMIM: 606401 CAPN9 Calpain 9 chr21_34690629_y_131 131 C21orf51 NM_058182 UTR chr22_24509538_y_131 131 MYO18B NM_032608 INTRON OMIM: 607295 MYO18B Myosin XVIIIB chr2_163811955_r_131 131 KCNH7 NM_033272 INTRON chr2_163811955_r_131 131 KCNH7 NM_173162 INTRON chr3_184245605_r_131 131 KIAA0861 NM_015078 INTRON chr4_8260628_r_131 131 ABLIM2 NM_032432 INTRON chr5_172709132_y_131 131 STC2 NM_003714 UTR chr8_30346500_y_131 131 RBPMS NM_006867 INTRON chr9_75713083_r_131 131 GNA14 NM_004297 INTRON OMIM: 604397 GNA14 Guanine nucleotide-binding protein, alpha-14 chrX_100301331_y_131 131 NXF2 NM_017809 UTR OMIM: 300315 NXF2 Nuclear RNA export factor 2 chrX_100301331_y_131 131 NXF2 NM_022053 UTR OMIM: 300315 NXF2 Nuclear RNA export factor 2 chrX_109392918_r_131 131 DCX NM_000555 INTRON OMIM: 300121 DCX, DBCN, LISX Doublecortin Lissencephaly, X-linked, 300067 (3); Subcortical laminalheteropia, X-linked, 300 MOUSE: X(Dcx) chrX_109392918_r_131 131 DCX NM_178151 INTRON OMIM: 300121 DCX, DBCN, LISX Doublecortin Lissencephaly, X-linked, 300067 (3); Subcortical laminalheteropia, X-linked, 300 MOUSE: X(Dcx) chrX_109392918_r_131 131 DCX NM_178152 INTRON OMIM: 300121 DCX, DBCN, LISX Doublecortin Lissencephaly, X-linked, 300067 (3); Subcortical laminalheteropia, X-linked, 300 MOUSE: X(Dcx) chrX_109392918_r_131 131 DCX NM_178153 INTRON OMIM: 300121 DCX, DBCN, LISX Doublecortin Lissencephaly, X-linked, 300067 (3); Subcortical laminalheteropia, X-linked, 300 MOUSE: X(Dcx) chr10_23222158_r_132 132 FLJ32827 NM_173081 UTR chr11_61396050_y_132 132 FADS2 NM_004265 INTRON chr15_67330812_r_132 132 MPRG NM_017705 UTR OMIM: 607781 MPRG Membrane progestin receptor, gamma chr16_3921290_r_132 132 CREBBP NM_004380 INTRON OMIM: 600140 CREBBP, CBP, RSTS CREB binding protein fusion partner with MORF in AML; fusion partner with MLL intherapy-related acute Rubenstein-Taybi syndrome, 180849 (3) chr17_10452869_y_132 132 MYH13 NM_003802 INTRON OMIM: 603487 MYH13 Myosin, heavy polypeptide 13, skeletal muscle MOUSE: 11(Myh13) chr18_54751378_y_132 132 FLJ10697 NM_018181 INTRON chr18_8230440_r_132 132 PTPRM NM_002845 INTRON OMIM: 176888 PTPRM, PTPRL1, RPTPM Protein tyrosine phosphatase, receptor type, mu polypeptide chr1_15844220_r_132 132 EPHA2 NM_004431 INTRON OMIM: 176946 EPHA2, ECK Ephrin receptor EphA2 MOUSE: 4(Epha2) chr1_159446353_y_132 132 CAPON NM_014697 INTRON OMIM: 605551 CAPON, KIAA0464 C-terminal PDZ domain ligand of neuronal nitric oxide synthase chr1_211846776_y_132 132 CENPF NM_016343 INTRON OMIM: 600236 CENPF Centromere autoantigen F, 400kD MOUSE: 1(Cenpf) chr1_22899778_r_132 132 LUZP1 NM_033631 UTR OMIM: 601422 LUZP1 Leucine zipper protein 1 MOUSE: 4(Luzp) chr1_56392540_r_132 132 PPAP2B NM_003713 INTRON chr1_56392540_r_132 132 PPAP2B NM_177414 INTRON chr1_84855965_r_132 132 MCOLN2 NM_153259 UTR OMIM: 607399 MCOLN2 Mucolipin 2 MOUSE: 3(Mcoln2) chr20_17285461_r_132 132 PCSK2 NM_002594 INTRON OMIM: 162151 PCSK2, NEC2, PC2 Proprotein convertase subtilisin/kexin type 2 MOUSE: 2(Nec2) chr2_131726695_r_132 132 FLJ38377 NM_152698 UTR chr2_162895539_r_132 132 SLC4A10 NM_022058 INTRON OMIM: 605556 SLC4A10 Solute carrier family 4 (sodium bicarbonate cotransporter-like),member 10 chr3_120661831_r_132 132 PLA1A NM_015900 INTRON OMIM: 607460 PLA1A, PSPLA1 Phosphatidylserine-specific phospholipase A1-alpha MOUSE: 16(Pla1a) chr3_99910428_r_132 132 ESDN NM_080927 INTRON chr4_110346827_r_132 132 COL25A1 NM_032518 INTRON chr4_177724855_y_132 132 WDR17 NM_170710 INTRON chr4_177724855_y_132 132 WDR17 NM_181265 UTR chr4_8289218_y_132 132 ABLIM2 NM_032432 INTRON chr5_134392224_y_132 132 CACRC NM_178019 INTRON chr5_142359012_y_132 132 GRAF NM_015071 INTRON OMIM: 605370 GRAF GTPase regulator associated with the focal adhesion kinase pp125 Leukemia, juvenile myelomonocytic, 607785 (3) chr5_158506740_r_132 132 EBF NM_024007 INTRON OMIM: 164343 EBF, OLF1 Early B-cell factor (olfactory neuronal transcription factor 1) MOUSE: 11(Ebf) chr5_31749514_y_132 132 PDZK3 NM_015022 UTR chr5_31749514_y_132 132 PDZK3 NM_178140 UTR chr5_43238877_y_132 132 MGC42105 NM_153361 UTR chr5_78807547_y_132 132 HOMER1 NM_004272 INTRON chr6_109405833_r_132 132 PA26 NM_014454 INTRON OMIM: 606103 PA26 p53-activated gene 26 MOUSE: 4(Pa26) chr6_42292438_r_132 132 TReP-132 NM_018415 UTR chr6_42292438_r_132 132 TReP-132 NM_033501 UTR chr6_42292438_r_132 132 TReP-132 NM_033502 UTR chr7_75247206_r_132 132 MK-STYX NM_016086 INTRON chr8_133356779_r_132 132 KCNQ3 NM_004519 INTRON OMIM: 602232 KCNQ3, EBN2, BFNC2 Potassium voltage-gated channel, KQT-like subfamily, member 3 Epilepsy, benign neonatal, type 2, 121201 (3) chr8_3896743_y_132 132 CSMD1 NM_033225 INTRON OMIM: 608397 CSMD1, KIAA1890 Cub and Sushi multiple domains 1 chr8_62302518_r_132 132 MGC34646 NM_173519 INTRON chr10_106241708_y_133 133 SORCS3 NM_014978 INTRON OMIM: 606285 SORCS3, KIAA1059 SORCS receptor 3 chr10_28216881_r_133 133 FLJ10817 NM_018076 INTRON chr13_112474609_y_133 133 GAS6 NM_000820 INTRON OMIM: 600441 GAS6, AXLLG, AXSF Growth arrest-specific 6 MOUSE: 8(Gas6) chr14_19762601_r_133 133 RPGRIP1 NM_020366 INTRON OMIM: 605446 RPGRIP1, LCA6, CORD9 Retinitis pigmentosa GTPase regulator-interacting protein Leber congenital amaurosis, 204000 (3); Cone-rod dystrophy 9,608194 (3) chr14_69999265_y_133 133 KIAA0440 NM_015556 UTR chr16_58133433_r_133 133 CSNK2A2 NM_001896 UTR OMIM: 115442 CSNK2A2 Casein kinase-2, alpha-prime polypeptide MOUSE: 8(Csnk2a2) chr19_14745084_y_133 133 EMR2 NM_013447 INTRON chr19_14745084_y_133 133 EMR2 NM_152916 INTRON chr19_14745084_y_133 133 EMR2 NM_152917 INTRON chr19_14745084_y_133 133 EMR2 NM_152918 INTRON chr19_14745084_y_133 133 EMR2 NM_152919 INTRON chr19_14745084_y_133 133 EMR2 NM_152920 INTRON chr19_14745084_y_133 133 EMR2 NM_152921 INTRON chr19_9955196_r_133 133 COL5A3 NM_015719 INTRON OMIM: 120216 COL5A3 Collagen, type V, alpha-3 polypeptide MOUSE: 9(Col5a3) chr1_206877595_r_133 133 LAMB3 NM_000228 INTRON OMIM: 150310 LAMB3 Laminin, beta-3 (nicein, 125kD; kalinin, 140kD; BM600, 125kD) Epidermolysis bullosa, Herlitz junctional type, 226700 (3);Epidermolysis bullosa chr1_57276833_y_133 133 DAB1 NM_021080 UTR OMIM: 603448 DAB1 Disabled, Drosophila, homolog 1 MOUSE: 4(Dab1) chr20_58132124_r_133 133 GNAS NM_016592 UTR OMIM: 139320 GNAS, GNAS1, GPSA, P GNAS complex locus (guanine nucleotide binding protein (G protein),alpha stimula Pseudohypoparathyroidism, type Ia, 103580 (3); McCune-Albrightsyndrome, 174800 ( MOUSE: 2(Gnas) chr20_58132124_r_133 133 GNAS NM_080425 INTRON OMIM: 139320 GNAS, GNAS1, GPSA, P GNAS complex locus (guanine nucleotide binding protein (G protein),alpha stimula Pseudohypoparathyroidism, type Ia, 103580 (3); McCune-Albrightsyndrome, 174800 ( MOUSE: 2(Gnas) chr22_40578819_r_133 133 C22orf18 NM_024053 INTRON chr2_159163973_r_133 133 LOC151531 NM_173355 INTRON chr2_69586360_r_133 133 GFPT1 NM_002056 INTRON chr2_9074153_r_133 133 LOC129642 NM_138799 UTR chr2_98486669_y_133 133 MGC26733 NM_144992 INTRON chr3_174066672_y_133 133 NYD-SP12 NM_031955 INTRON chr4_47092403_y_133 133 GABRB1 NM_000812 INTRON OMIM: 137190 GABRB1 Gamma-aminobutyric acid (GABA) A receptor, beta-1 MOUSE: 5(Gabrb1) chr4_47092403_y_133 133 COX7B2 NM_130902 UTR chr6_37911130_y_133 133 TEX27 NM_021943 INTRON chr6_38450185_y_133 133 BTBD9 NM_152733 INTRON chr8_53092566_r_133 133 ST18 NM_014682 INTRON chr9_3356623_y_133 133 RFX3 NM_134428 INTRON chr9_3356623_y_133 133 RFX3 NM_002919 INTRON chr9_81551319_r_133 133 MGC20553 NM_174938 INTRON chrX_121092033_r_133 133 GRIA3 NM_000828 INTRON OMIM: 305915 GRIA3, GLUR3 Glutamate receptor, ionotropic, AMPA 3 MOUSE: X(Glur3) chrX_121092033_r_133 133 GRIA3 NM_007325 INTRON OMIM: 305915 GRIA3, GLUR3 Glutamate receptor, ionotropic, AMPA 3 MOUSE: X(Glur3) chrX_66509384_r_133 133 OPHN1 NM_002547 INTRON OMIM: 300127 OPHN1 Oligophrenin-1 Mental retardation, X-linked, 60 (3) chr10_35550115_y_134 134 CFP1 NM_181698 UTR chr11_48129629_y_134 134 PTPRJ NM_002843 INTRON OMIM: 600925 PTPRJ, DEP1 Protein tyrosine phosphatase, receptor type, J polypeptide Colon cancer, somatic, 114500 (3) MOUSE: 2(Ptprj) chr11_76769671_r_134 134 PAK1 NM_002576 INTRON OMIM: 602590 PAK1 p21/CDC42/RAC1-activated kinase 1 chr12_113219990_r_134 134 TBX5 NM_181486 INTRON OMIM: 601620 TBX5 T-box 5 Holt-Oram syndrome, 142900 (3) MOUSE: 5(Tbx5) chr12_113219990_r_134 134 TBX5 NM_000192 INTRON OMIM: 601620 TBX5 T-box 5 Holt-Oram syndrome, 142900 (3) MOUSE: 5(Tbx5) chr12_113219990_r_134 134 TBX5 NM_080717 INTRON OMIM: 601620 TBX5 T-box 5 Holt-Oram syndrome, 142900 (3) MOUSE: 5(Tbx5) chr12_113219990_r_134 134 TBX5 NM_080718 INTRON OMIM: 601620 TBX5 T-box 5 Holt-Oram syndrome, 142900 (3) MOUSE: 5(Tbx5) chr12_38668678_r_134 134 SLC2A13 NM_052885 INTRON chr14_93593500_r_134 134 DICER1 NM_030621 UTR chr14_93593500_r_134 134 DICER1 NM_177438 UTR chr16_20977819_r_134 134 DKFZp434N074 NM_017539 INTRON chr16_83313747_y_134 134 CDH13 NM_001257 INTRON OMIM: 601364 CDH13, CDHH Cadherin-13 (H-cadherin, heart) chr18_8230596_r_134 134 PTPRM NM_002845 INTRON OMIM: 176888 PTPRM, PTPRL1, RPTPM Protein tyrosine phosphatase, receptor type, mu polypeptide chr19_13227484_y_134 134 CACNA1A NM_000068 INTRON OMIM: 601011 CACNA1A, CACNL1A4, S Calcium channel, voltage-dependent, P/Q type, alpha 1A subunit Hemiplegic migraine, familial, 141500 (3); Episodic ataxia, type 2,108500 (3); S MOUSE: 8(tg, Cacl1a4) chr19_13227484_y_134 134 CACNA1A NM_023035 INTRON OMIM: 601011 CACNA1A, CACNL1A4, S Calcium channel, voltage-dependent, P/Q type, alpha 1A subunit Hemiplegic migraine, familial, 141500 (3); Episodic ataxia, type 2,108500 (3); S MOUSE: 8(tg, Cacl1a4) chr1_115174991_y_134 134 NGFB NM_002506 UTR OMIM: 162030 NGFB Nerve growth factor, beta same 310kb fragment as TSHB;order: cen-CD2-CD58-ATP1A1-NGF-TSHB-NRAS-tel MOUSE: 3(Ngfb) chr1_17397083_y_134 134 FLJ10521 NM_018125 INTRON chr1_59682078_y_134 134 HOOK1 NM_015888 INTRON chr22_28829457_y_134 134 MGC26710 NM_152510 INTRON chr3_121007492_y_134 134 GSK3B NM_002093 INTRON OMIM: 605004 GSK3B Glycogen synthase kinase 3-beta chr3_152338016_y_134 134 TRALPUSH NM_053002 INTRON chr3_152338016_y_134 134 GPR87 NM_023915 INTRON OMIM: 606379 GPR87 G protein-coupled receptor 87 chr3_31825973_r_134 134 OSBPL10 NM_017784 INTRON OMIM: 606738 OSBPL10, ORP10 Oxysterol-binding protein-like protein 10 chr4_106970015_r_134 134 FLJ20184 NM_017700 INTRON chr5_149278913_r_134 134 PDE6A NM_000440 INTRON OMIM: 180071 PDE6A, PDEA Phosphodiesterase-6A, cGMP-specific, rod, alpha Retinitis pigmentosa, autosomal recessive (3) MOUSE: 18(Pde6a) chr5_63815289_r_134 134 FLJ36754 NM_173829 UTR chr6_119395705_y_134 134 C6orf60 NM_024581 UTR chr7_116162805_y_134 134 ST7 NM_021908 INTRON OMIM: 600833 ST7, TSG7, RAY1, FAM Suppressor of tumorigenicity 7 (breast) chr7_116162805_y_134 134 ST7 NM_018412 INTRON OMIM: 600833 ST7, TSG7, RAY1, FAM Suppressor of tumorigenicity 7 (breast) chr7_81427530_r_134 134 CACNA2D1 NM_000722 INTRON chr8_145232039_y_134 134 PLEC1 NM_000445 UTR OMIM: 601282 PLEC1, PLTN, EBS1 Plectin 1, intermediate filament binding protein, 500kD Muscular dystrophy with epidermolysis bullosa simplex, 226670 (3);Epidermolysis chr8_6523782_r_134 134 ANGPT2 NM_001147 UTR OMIM: 601922 ANGPT2, ANG2 Angiopoietin 2 close to MCPH1 MOUSE: 8(Angpt2) chr9_131864254_r_134 134 DBH NM_000787 INTRON OMIM: 223360 DBH Dopamine-beta-hydroxylase tightly linked to ABO [Dopamine-beta-hydroxylase activity levels, plasma] (3) MOUSE: 2(Dbh) chr12_39493083_y_135 135 CNTN1 NM_001843 UTR OMIM: 600016 CNTN1 Contactin 1 chr12_39493083_y_135 135 CNTN1 NM_175038 UTR OMIM: 600016 CNTN1 Contactin 1 chr15_27064806_y_135 135 APBA2 NM_005503 INTRON OMIM: 602712 APBA2 Amyloid beta A4 precursor protein-binding, family A, member 2 MOUSE: 7(Apba2) chr17_16424072_r_135 135 PIGL NM_004278 INTRON OMIM: 605947 PIGL Phosphatidylinositol glycan, class L chr17_31937016_y_135 135 ACCN1 NM_001094 INTRON OMIM: 601784 ACCN1, BNC1, MDEG Amiloride-sensitive cation channel 1, neuronal (degenerin) chr17_42209515_y_135 135 MEOX1 NM_004527 INTRON OMIM: 600147 MEOX1, MOX1 Mesenchyme homeo box 1 (Mox1, mouse, homolog of) chr17_42209515_y_135 135 MEOX1 NM_013999 INTRON OMIM: 600147 MEOX1, MOX1 Mesenchyme homeo box 1 (Mox1, mouse, homolog of) chr17_5646596_y_135 135 DEFCAP NM_033004 INTRON OMIM: 606636 DEFCAP, KIAA0926, NA Death effector filament-forming CED4-like apoptosis protein chr17_5646596_y_135 135 DEFCAP NM_014922 INTRON OMIM: 606636 DEFCAP, KIAA0926, NA Death effector filament-forming CED4-like apoptosis protein chr17_5646596_y_135 135 DEFCAP NM_033005 INTRON OMIM: 606636 DEFCAP, KIAA0926, NA Death effector filament-forming CED4-like apoptosis protein chr17_5646596_y_135 135 DEFCAP NM_033006 INTRON OMIM: 606636 DEFCAP, KIAA0926, NA Death effector filament-forming CED4-like apoptosis protein chr17_5646596_y_135 135 DEFCAP NM_033007 INTRON OMIM: 606636 DEFCAP, KIAA0926, NA Death effector filament-forming CED4-like apoptosis protein chr19_6765621_y_135 135 TRIP10 NM_004240 UTR chr19_6765621_y_135 135 VAV1 NM_005428 INTRON OMIM: 164875 VAV1, VAV Oncogene VAV1 close to INSR chr1_211846640_y_135 135 CENPF NM_016343 INTRON OMIM: 600236 CENPF Centromere autoantigen F, 400kD MOUSE: 1(Cenpf) chr1_52091486_y_135 135 MADHIP NM_007323 INTRON chr1_52091486_y_135 135 MADHIP NM_007324 INTRON chr1_52091486_y_135 135 MADHIP NM_004799 INTRON chr1_99827983_y_135 135 AGL NM_000642 INTRON OMIM: 232400 AGL, GDE Amylo-1,6-glucosidase, 4-alpha-glucanotransferase (glycogendebranching enzyme) Glycogen storage disease IIIa (3); Glycogen storage disease IIIb (3) chr1_99827983_y_135 135 AGL NM_000028 INTRON OMIM: 232400 AGL, GDE Amylo-1,6-glucosidase, 4-alpha-glucanotransferase (glycogendebranching enzyme) Glycogen storage disease IIIa (3); Glycogen storage disease IIIb (3) chr1_99827983_y_135 135 AGL NM_000643 INTRON OMIM: 232400 AGL, GDE Amylo-1,6-glucosidase, 4-alpha-glucanotransferase (glycogendebranching enzyme) Glycogen storage disease IIIa (3); Glycogen storage disease IIIb (3) chr1_99827983_y_135 135 AGL NM_000644 INTRON OMIM: 232400 AGL, GDE Amylo-1,6-glucosidase, 4-alpha-glucanotransferase (glycogendebranching enzyme) Glycogen storage disease IIIa (3); Glycogen storage disease IIIb (3) chr1_99827983_y_135 135 AGL NM_000646 INTRON OMIM: 232400 AGL, GDE Amylo-1,6-glucosidase, 4-alpha-glucanotransferase (glycogendebranching enzyme) Glycogen storage disease IIIa (3); Glycogen storage disease IIIb (3) chr1_99827983_y_135 135 AGL NM_000645 INTRON OMIM: 232400 AGL, GDE Amylo-1,6-glucosidase, 4-alpha-glucanotransferase (glycogendebranching enzyme) Glycogen storage disease IIIa (3); Glycogen storage disease IIIb (3) chr20_34256980_y_135 135 GSS NM_000178 UTR OMIM: 601002 GSS, GSHS Glutathione synthetase Hemolytic anemia due to glutathione synthetase deficiency, 231900(3); 5-oxoproli chr20_8515263_y_135 135 PLCB1 NM_015192 INTRON chr2_114107913_r_135 135 PAX8 NM_013952 INTRON OMIM: 167415 PAX8 Paired box homeotic gene-8 Hypothyroidism, congenital, due to thyroid dysgenesis orhypoplasia, 218700 (3) MOUSE: 2(Pax8) chr2_114107913_r_135 135 PAX8 NM_013953 INTRON OMIM: 167415 PAX8 Paired box homeotic gene-8 Hypothyroidism, congenital, due to thyroid dysgenesis orhypoplasia, 218700 (3) MOUSE: 2(Pax8) chr2_114107913_r_135 135 PAX8 NM_013992 INTRON OMIM: 167415 PAX8 Paired box homeotic gene-8 Hypothyroidism, congenital, due to thyroid dysgenesis orhypoplasia, 218700 (3) MOUSE: 2(Pax8) chr2_114107913_r_135 135 PAX8 NM_003466 INTRON OMIM: 167415 PAX8 Paired box homeotic gene-8 Hypothyroidism, congenital, due to thyroid dysgenesis orhypoplasia, 218700 (3) MOUSE: 2(Pax8) chr2_114107913_r_135 135 PAX8 NM_013951 INTRON OMIM: 167415 PAX8 Paired box homeotic gene-8 Hypothyroidism, congenital, due to thyroid dysgenesis orhypoplasia, 218700 (3) MOUSE: 2(Pax8) chr2_183329386_y_135 135 PDE1A NM_005019 INTRON OMIM: 171890 PDE1A Phosphodiesterase-1A chr3_174606832_y_135 135 NLGN1 NM_014932 UTR OMIM: 600568 NLGN1 Neuroligin 1 chr4_167550003_y_135 135 TLL1 NM_012464 INTRON OMIM: 606742 TLL1, TLL Tolloid-like 1 MOUSE: 8(Tll1) chr6_151878196_y_135 135 C6orf97 NM_025059 INTRON chr6_157853209_y_135 135 ZDHHC14 NM_024630 INTRON chr6_157853209_y_135 135 ZDHHC14 NM_153746 INTRON chr6_6452682_r_135 135 FLJ33708 NM_173675 UTR chr8_141728551_r_135 135 PTK2 NM_005607 INTRON OMIM: 601212 PTK2B, FAK2, PYK2 Protein tyrosine kinase-2, beta (focal adhesion kinase 2) chr8_141728551_r_135 135 PTK2 NM_153831 INTRON OMIM: 601212 PTK2B, FAK2, PYK2 Protein tyrosine kinase-2, beta (focal adhesion kinase 2) chr9_6929977_y_135 135 GASC1 NM_015061 INTRON OMIM: 605469 GASC1 Gene amplified in squamous cell carcinoma-1 chrX_10145420_r_135 135 MID1 NM_033290 UTR OMIM: 300000 MID1, OGS1, BBBG1, F Midline-1 type II defect on chr.22 Opitz G syndrome, type I (3) MOUSE: X(Mid1) chrX_43973969_y_135 135 UTX NM_021140 INTRON OMIM: 300128 UTX Ubiquitously-transcribed TPR gene on X chromosome UTY also in mouse and man; escapes inactivation MOUSE: X(Utx) chr10_104923718_y_136 136 NEURL NM_004210 INTRON OMIM: 603804 NEURL Neuralized, Drosophila, homolog-like chr10_6551431_y_136 136 PRKCQ NM_006257 INTRON OMIM: 600448 PRKCQ Protein kinase C, theta MOUSE: 2(Pkcq) chr11_84037451_r_136 136 DLG2 NM_001364 INTRON OMIM: 603583 DLG2 Discs large, Drosophila, homolog of, 2(channel-associated protein of synapses, 1 chr15_55413986_y_136 136 FLJ14957 NM_032866 UTR chr16_19468581_y_136 136 TMC5 NM_024780 INTRON chr17_64206636_y_136 136 MGC33887 NM_145036 INTRON chr17_64767515_r_136 136 APOH NM_000042 INTRON OMIM: 138700 APOH Apolipoprotein H (beta-2-glycoprotein I) [Apolipoprotein H deficiency] (3) MOUSE: 11(Apoh) chr17_67891494_r_136 136 ABCA5 NM_018672 INTRON chr17_67891494_r_136 136 ABCA5 NM_172232 INTRON chr19_2553926_y_136 136 FLJ00058 NM_052847 UTR chr19_3028965_r_136 136 GNA11 NM_002067 UTR OMIM: 139313 GNA11 Guanine nucleotide-binding protein, Gq class, GNA11 MOUSE: 10(Gna11) chr1_195009251_r_136 136 MGC27044 NM_144977 UTR chr1_232616585_y_136 136 TBCE NM_003193 INTRON OMIM: 604934 TBCE, KCS, KCS1, HRD Tubulin-specific chaperone E Kenny-Caffey syndrome-1, 244460 (3);Hypoparathyroidism-retardation-dysmorphism s chr1_238753612_r_136 136 KMO NM_003679 INTRON OMIM: 603538 KMO Kynurenine 3-monooxygenase chr22_42785203_y_136 136 PARVB NM_013327 INTRON chr3_54814105_y_136 136 CACNA2D3 NM_018398 INTRON OMIM: 606399 CACNA2D3 Calcium channel, voltage-dependent, alpha-2/delta subunit 3 chr3_78688827_r_136 136 ROBO1 NM_133631 INTRON OMIM: 602430 ROBO1, DUTT1, SAX3 Roudnabout, Drosophila, homolog of, 1 chr3_78688827_r_136 136 ROBO1 NM_002941 INTRON OMIM: 602430 ROBO1, DUTT1, SAX3 Roudnabout, Drosophila, homolog of, 1 chr5_147172957_r_136 136 KIAA0555 NM_014790 UTR chr5_149492412_r_136 136 CSF1R NM_005211 INTRON OMIM: 164770 CSF1R, FMS Colony-stimulating factor-1 receptor; oncogene FMS (McDonoughfeline sarcoma) FMS2 is 5' end Myeloid malignancy, predisposition to (3) MOUSE: 18(Fim2) chr5_150748126_r_136 136 SLC36A2 NM_181776 INTRON chr5_75876599_y_136 136 IQGAP2 NM_006633 INTRON OMIM: 605401 IQGAP2 IQ motif-containing GTPase-activating protein-2 chr6_20838592_r_136 136 CDKAL1 NM_017774 INTRON chr6_43056597_r_136 136 KIAA0076 NM_014780 INTRON chr7_70557862_y_136 136 WBSCR17 NM_022479 INTRON chr7_71877948_r_136 136 FKBP6 NM_003602 INTRON OMIM: 604839 FKBP6 FK506-binding protein 6 chr7_71877948_r_136 136 DKFZP434A0131 NM_018991 UTR chr7_74611027_y_136 136 DKFZP434A0131 NM_018991 UTR chr8_61570993_y_136 136 RAB2 NM_002865 INTRON OMIM: 602306 RAB2L RAB2, member RAS oncogene family-like chr10_134379539_r_137 137 GPR123 NM_032422 INTRON chr10_30746806_r_137 137 MAP3K8 NM_005204 INTRON OMIM: 191195 MAP3K8, COT, EST, TP Mitogen-activated protein kinase kinase kinase 8(cancer Osaka thyroid oncogene) MOUSE: 18(Tpl2) chr10_71040423_r_137 137 COL13A1 NM_005203 INTRON OMIM: 120350 COL13A1 Collagen XIII, alpha-1 polypeptide ~550kb proximal to P4HA chr10_71040423_r_137 137 COL13A1 NM_080798 INTRON OMIM: 120350 COL13A1 Collagen XIII, alpha-1 polypeptide ~550kb proximal to P4HA chr10_71040423_r_137 137 COL13A1 NM_080799 INTRON OMIM: 120350 COL13A1 Collagen XIII, alpha-1 polypeptide ~550kb proximal to P4HA chr10_71040423_r_137 137 COL13A1 NM_080800 INTRON OMIM: 120350 COL13A1 Collagen XIII, alpha-1 polypeptide ~550kb proximal to P4HA chr10_71040423_r_137 137 COL13A1 NM_080801 INTRON OMIM: 120350 COL13A1 Collagen XIII, alpha-1 polypeptide ~550kb proximal to P4HA chr10_71040423_r_137 137 COL13A1 NM_080802 INTRON OMIM: 120350 COL13A1 Collagen XIII, alpha-1 polypeptide ~550kb proximal to P4HA chr10_71040423_r_137 137 COL13A1 NM_080803 INTRON OMIM: 120350 COL13A1 Collagen XIII, alpha-1 polypeptide ~550kb proximal to P4HA chr10_71040423_r_137 137 COL13A1 NM_080804 INTRON OMIM: 120350 COL13A1 Collagen XIII, alpha-1 polypeptide ~550kb proximal to P4HA chr10_71040423_r_137 137 COL13A1 NM_080805 INTRON OMIM: 120350 COL13A1 Collagen XIII, alpha-1 polypeptide ~550kb proximal to P4HA chr10_71040423_r_137 137 COL13A1 NM_080806 INTRON OMIM: 120350 COL13A1 Collagen XIII, alpha-1 polypeptide ~550kb proximal to P4HA chr10_71040423_r_137 137 COL13A1 NM_080807 INTRON OMIM: 120350 COL13A1 Collagen XIII, alpha-1 polypeptide ~550kb proximal to P4HA chr10_71040423_r_137 137 COL13A1 NM_080808 INTRON OMIM: 120350 COL13A1 Collagen XIII, alpha-1 polypeptide ~550kb proximal to P4HA chr10_71040423_r_137 137 COL13A1 NM_080809 INTRON OMIM: 120350 COL13A1 Collagen XIII, alpha-1 polypeptide ~550kb proximal to P4HA chr10_71040423_r_137 137 COL13A1 NM_080810 INTRON OMIM: 120350 COL13A1 Collagen XIII, alpha-1 polypeptide ~550kb proximal to P4HA chr10_71040423_r_137 137 COL13A1 NM_080811 INTRON OMIM: 120350 COL13A1 Collagen XIII, alpha-1 polypeptide ~550kb proximal to P4HA chr10_71040423_r_137 137 COL13A1 NM_080812 INTRON OMIM: 120350 COL13A1 Collagen XIII, alpha-1 polypeptide ~550kb proximal to P4HA chr10_71040423_r_137 137 COL13A1 NM_080813 INTRON OMIM: 120350 COL13A1 Collagen XIII, alpha-1 polypeptide ~550kb proximal to P4HA chr10_71040423_r_137 137 COL13A1 NM_080814 INTRON OMIM: 120350 COL13A1 Collagen XIII, alpha-1 polypeptide ~550kb proximal to P4HA chr10_71040423_r_137 137 COL13A1 NM_080815 INTRON OMIM: 120350 COL13A1 Collagen XIII, alpha-1 polypeptide ~550kb proximal to P4HA chr15_66677211_r_137 137 CORO2B NM_006091 INTRON OMIM: 605002 CORO2B, CLIPINC Coronin 2B chr16_19442877_y_137 137 TMC5 NM_024780 INTRON chr17_37660831_r_137 137 TEM7 NM_020405 INTRON OMIM: 606827 TEM7R Tumor endothelial marker 7-related protein chr1_115650397_r_137 137 CASQ2 NM_001232 INTRON OMIM: 114251 CASQ2 Calsequestrin, fast-twitch, skeletal muscle-2 Ventricular tachycardia, stress-induced polymorphic, 604772 (3) chr20_51469428_y_137 137 ZFP64 NM_022088 INTRON chr20_51469428_y_137 137 ZFP64 NM_018197 INTRON chr22_35282167_y_137 137 CACNG2 NM_006078 INTRON OMIM: 602911 CACNG2 Calcium channel, voltage-dependent, gamma-2 subunit MOUSE: 15(Cacng2) chr2_197112400_r_137 137 DNAH7 NM_018897 INTRON chr2_228261191_r_137 137 COL4A3 NM_000091 INTRON OMIM: 120070 COL4A3 Collagen IV, alpha-3 polypeptide (Goodpasture antigen) noncollagenous domain = Goodpasture antigen Alport syndrome, autosomal recessive, 203780 (3) chr2_228261191_r_137 137 COL4A3 NM_031362 INTRON OMIM: 120070 COL4A3 Collagen IV, alpha-3 polypeptide (Goodpasture antigen) noncollagenous domain = Goodpasture antigen Alport syndrome, autosomal recessive, 203780 (3) chr2_228261191_r_137 137 COL4A3 NM_031363 INTRON OMIM: 120070 COL4A3 Collagen IV, alpha-3 polypeptide (Goodpasture antigen) noncollagenous domain = Goodpasture antigen Alport syndrome, autosomal recessive, 203780 (3) chr2_228261191_r_137 137 COL4A3 NM_031364 INTRON OMIM: 120070 COL4A3 Collagen IV, alpha-3 polypeptide (Goodpasture antigen) noncollagenous domain = Goodpasture antigen Alport syndrome, autosomal recessive, 203780 (3) chr2_228261191_r_137 137 COL4A3 NM_031365 INTRON OMIM: 120070 COL4A3 Collagen IV, alpha-3 polypeptide (Goodpasture antigen) noncollagenous domain = Goodpasture antigen Alport syndrome, autosomal recessive, 203780 (3) chr2_228261191_r_137 137 COL4A3 NM_031366 INTRON OMIM: 120070 COL4A3 Collagen IV, alpha-3 polypeptide (Goodpasture antigen) noncollagenous domain = Goodpasture antigen Alport syndrome, autosomal recessive, 203780 (3) chr2_29999870_r_137 137 ALK NM_004304 INTRON OMIM: 105590 ALK Anaplastic lymphoma kinase (Ki-1) MOUSE: 17(Alk) chr4_119618090_r_137 137 NDST3 NM_004784 INTRON chr5_16849094_r_137 137 MYO10 NM_012334 INTRON OMIM: 601481 MYO10 Myosin X MOUSE: 15(Myo10) chr7_73216518_r_137 137 CYLN2 NM_003388 INTRON OMIM: 603432 CYLN2, WBSCR4, WSCR4 Cytoplasmic linker 2 ?neurodevelpmental defect of Williams syndrome MOUSE: 5(Cyln2) chr7_73216518_r_137 137 CYLN2 NM_032421 INTRON OMIM: 603432 CYLN2, WBSCR4, WSCR4 Cytoplasmic linker 2 ?neurodevelpmental defect of Williams syndrome MOUSE: 5(Cyln2) chr8_32359157_y_137 137 NRG1 NM_013962 INTRON OMIM: 142445 NRG1, HGL, HRGA, ARI Neuregulin 1 (heregulin, alpha, 45kD; ERBB2 p185-activator) {?Schizophrenia, susceptibility to}, 603013 (1) MOUSE: 7(Nrg1) chr8_51622696_r_137 137 SNTG1 NM_018967 INTRON chrX_9588801_y_137 137 CLCN4 NM_001830 INTRON OMIM: 302910 CLCN4 Chloride channel-4 chr10_117991199_y_138 138 PNLIP NM_000936 INTRON OMIM: 246600 PNLIP Pancreatic lipase Pancreatic lipase deficiency (1) chr10_1506258_y_138 138 ADARB2 NM_018702 INTRON OMIM: 602065 ADARB2, RED2 Adenosine deaminase, RNA-specific, B2 (homolog of rat BLUE) chr10_73302656_r_138 138 CGI-18 NM_015947 INTRON chr11_14711112_y_138 138 PDE3B NM_000922 INTRON OMIM: 602047 PDE3B Phosphodiesterase-3B, cGMP-inhibited chr12_123133715_y_138 138 LOC144347 NM_181709 UTR chr12_78204781_r_138 138 SYT1 NM_005639 INTRON OMIM: 608081 SYT15 Synaptotagmin 15 MOUSE: 14(Syt15) chr13_34239978_r_138 138 DCAMKL1 NM_004734 INTRON OMIM: 604742 DCAMKL1 Doublecortin- and calmodulin kinase-like 1 chr13_40564664_y_138 138 DGKH NM_152910 INTRON chr13_40564664_y_138 138 DGKH NM_178009 INTRON chr13_94624159_y_138 138 HS6ST3 NM_153456 INTRON chr15_83179528_y_138 138 SLC28A1 NM_004213 INTRON OMIM: 606207 SLC28A1, CNT1 Solute carrier family 28 (sodium-coupled nucleoside transporter),member 1 chr17_6694859_r_138 138 KIAA0753 NM_014804 INTRON chr1_182070204_r_138 138 C1orf24 NM_052966 INTRON chr1_182070204_r_138 138 C1orf24 NM_022083 UTR chr1_39175695_r_138 138 MACF1 NM_012090 INTRON chr1_50325972_r_138 138 FAF1 NM_007051 INTRON chr1_50325972_r_138 138 FAF1 NM_131917 INTRON chr3_160488572_r_138 138 SCHIP1 NM_014575 INTRON chr3_171150047_r_138 138 PHC3 NM_024947 INTRON chr3_186404554_y_138 138 MAP3K13 NM_004721 UTR OMIM: 604915 MAP3K13, LZK Mitogen-activated protein kinase kinase kinase 13 (leucinezipper-bearing kinase) chr4_129445230_y_138 138 FLJ10378 NM_032239 UTR chr4_129445230_y_138 138 FLJ10378 NM_178043 UTR chr4_129445230_y_138 138 FLJ10378 NM_018078 UTR chr4_186293893_y_138 138 FLJ33167 NM_152683 INTRON chr4_47856506_r_138 138 CNGA1 NM_000087 INTRON OMIM: 123825 CNGA1, CNCG1 Cyclic nucleotide gated channel, alpha 1 Retinitis pigmentosa, autosomal recessive (3) MOUSE: 5(Cncg) chr4_74817509_r_138 138 AFM NM_001133 INTRON OMIM: 104145 AFM, ALBA, ALB2 Afamin 10kb 3' of AFP chr5_146037767_y_138 138 PPP2R2B NM_004576 INTRON OMIM: 604325 PPP2R2B Protein phosphatase 2, regulatory subunit B, beta Spinocerebellar ataxia 12, 604326 (3) chr5_146037767_y_138 138 PPP2R2B NM_181675 INTRON OMIM: 604325 PPP2R2B Protein phosphatase 2, regulatory subunit B, beta Spinocerebellar ataxia 12, 604326 (3) chr5_146037767_y_138 138 PPP2R2B NM_181676 INTRON OMIM: 604325 PPP2R2B Protein phosphatase 2, regulatory subunit B, beta Spinocerebellar ataxia 12, 604326 (3) chr5_146037767_y_138 138 PPP2R2B NM_181674 INTRON OMIM: 604325 PPP2R2B Protein phosphatase 2, regulatory subunit B, beta Spinocerebellar ataxia 12, 604326 (3) chr5_146037767_y_138 138 PPP2R2B NM_181677 INTRON OMIM: 604325 PPP2R2B Protein phosphatase 2, regulatory subunit B, beta Spinocerebellar ataxia 12, 604326 (3) chr5_146037767_y_138 138 PPP2R2B NM_181678 INTRON OMIM: 604325 PPP2R2B Protein phosphatase 2, regulatory subunit B, beta Spinocerebellar ataxia 12, 604326 (3) chr6_144457648_y_138 138 STX11 NM_003764 UTR chr7_102974070_y_138 138 RELN NM_005045 INTRON OMIM: 600514 RELN, RL Reelin Lissencephaly syndrome, Norman-Roberts type, 257320 (3) MOUSE: 5(rl) chr7_102974070_y_138 138 RELN NM_173054 INTRON OMIM: 600514 RELN, RL Reelin Lissencephaly syndrome, Norman-Roberts type, 257320 (3) MOUSE: 5(rl) chr7_40157502_y_138 138 C7orf10 NM_024728 INTRON chr7_41749047_r_138 138 GLI3 NM_000168 INTRON OMIM: 165240 GLI3, PAPA, PAPB GLI-Kruppel family member GLI3 (oncogene GLI3) amplified in glioblastoma Greig cephalopolysyndactyly syndrome, 175700 (3); Pallister-Hallsyndrome, 146510 MOUSE: 13(Xt) chr7_71964032_r_138 138 FKBP6 NM_003602 INTRON OMIM: 604839 FKBP6 FK506-binding protein 6 chr7_73957977_y_138 138 GTF2IRD2 NM_173537 INTRON chr8_118942612_r_138 138 EXT1 NM_000127 INTRON OMIM: 608177 EXT1 Exostosin 1 distal to TRPS1 Exostoses, multiple, type 1, 133700 (3); Chondrosarcoma, 215300 (3) MOUSE: 15(Ext1) chrX_107488092_r_138 138 GUCY2F NM_001522 UTR OMIM: 300041 GUCY2F, GUC2F Guanylate cyclase 2F MOUSE: X(Gucy2f) chr10_15104916_y_139 139 FLJ11106 NM_018324 INTRON chr10_20439343_y_139 139 TEM7R NM_032812 INTRON OMIM: 606827 TEM7R Tumor endothelial marker 7-related protein chr10_38137819_y_139 139 LOC57209 NM_021045 INTRON chr11_98816816_r_139 139 CNTN5 NM_014361 UTR OMIM: 607219 CNTN5, NB2 Contactin 5 chr11_98816816_r_139 139 CNTN5 NM_175566 UTR OMIM: 607219 CNTN5, NB2 Contactin 5 chr12_48815142_r_139 139 LOC91012 NM_147190 INTRON chr12_80110010_y_139 139 FLJ21963 NM_024560 INTRON chr16_57284970_y_139 139 DOK4 NM_018110 INTRON OMIM: 608333 DOK4 Docking protein 4 chr16_7391494_y_139 139 A2BP1 NM_018723 INTRON chr16_7391494_y_139 139 A2BP1 NM_145891 INTRON chr16_7391494_y_139 139 A2BP1 NM_145892 INTRON chr16_7391494_y_139 139 A2BP1 NM_145893 INTRON chr19_8532395_y_139 139 MYO1F NM_012335 INTRON OMIM: 601480 MYO1F Myosin IF MOUSE: 17(Myo1f) chr20_4986831_r_139 139 SLC23A2 NM_005116 UTR OMIM: 603791 SLC23A2, SVCT2 Solute carrier family 23 (nucleobase transporters), member 2(sodium-dependent vi chr2_198692926_y_139 139 FLJ30574 NM_144629 INTRON chr3_112870673_r_139 139 FLJ31579 NM_153268 INTRON chr3_127802960_y_139 139 MGC13016 NM_032343 INTRON chr5_169423680_y_139 139 DOCK2 NM_004946 INTRON chr5_93974705_y_139 139 MGC34713 NM_173665 UTR chr6_24750379_r_139 139 KIAA0319 NM_014809 UTR chr7_100338668_r_139 139 SERPINE1 NM_000602 INTRON chr7_129707405_r_139 139 COPG2 NM_012133 INTRON OMIM: 604355 COPG2 Coatomer protein complex, subunit gamma-2 chr7_131663436_y_139 139 DKFZp434G0625 NM_181775 UTR chr7_70667391_r_139 139 CALN1 NM_031468 INTRON chr7_95482310_r_139 139 SLC25A13 NM_014251 INTRON OMIM: 603859 SLC25A13, CTLN2 Solute carrier family 25 (mitochondrial carrier, citrin), member 13 Citrullinemia, adult-onset type II, 603471 (3); Citrullinemia,type II, neonatal- chr9_34406169_r_139 139 C9orf25 NM_147202 INTRON chrX_1377318_y_139 139 ASMT NM_004043 UTR OMIM: 300015 ASMT, HIOMT Acetylserotonin methyltransferase pseudoautosomal chrY_1377318_y_139 139 ASMT NM_004043 UTR OMIM: 300015 ASMT, HIOMT Acetylserotonin methyltransferase pseudoautosomal chr10_100219307_r_140 140 HPSE2 NM_021828 INTRON chr10_106301047_y_140 140 SORCS3 NM_014978 INTRON OMIM: 606285 SORCS3, KIAA1059 SORCS receptor 3 chr10_34554623_r_140 140 PARD3 NM_019619 INTRON OMIM: 606745 PARD3, PAR3 Partitioning-defective protein 3, C. elegans, homolog of chr14_28667518_r_140 140 PRKCM NM_002742 UTR OMIM: 605435 PRKCM Protein kinase C, mu also assigned to chr.21 chr16_88273027_y_140 140 ZFPM1 NM_153813 INTRON OMIM: 601950 ZFPM1, FOG, FOG1 Zinc finger protein, multitype 1(friend of GATA1) chr17_4560118_y_140 140 MGC29671 NM_182538 INTRON chr17_74057790_y_140 140 KIAA0195 NM_014738 UTR chr18_19930309_y_140 140 FLJ33761 NM_153211 INTRON chr18_3541655_y_140 140 DLGAP1 NM_004746 INTRON chr19_59101088_y_140 140 PRKCG NM_002739 INTRON OMIM: 176980 PRKCG, PKCC, PKCG, S Protein kinase C, gamma polypeptide Spinocerebellar ataxia 14, 605361 (3) MOUSE: 7(Pkcc) chr1_154947207_r_140 140 SPAP1 NM_030764 INTRON OMIM: 606509 SPAP1, SPAP1A, SPAP1 SH2 domain-containing phosphatase anchor protein 1 chr1_154947207_r_140 140 SPAP1 NM_138738 INTRON OMIM: 606509 SPAP1, SPAP1A, SPAP1 SH2 domain-containing phosphatase anchor protein 1 chr2_32660671_y_140 140 BIRC6 NM_016252 INTRON OMIM: 605638 BIRC6, KIAA1289 Baculoviral IAP repeat-containing protein-6 chr3_13885025_r_140 140 WNT7A NM_004625 INTRON OMIM: 601570 WNT7A Wingless-type MMTV integration site family, member 7A chr3_186561127_r_140 140 LIPH NM_139248 INTRON OMIM: 607365 LIPH Lipase H chr4_141572907_r_140 140 MAML3 NM_018717 INTRON chr5_149649764_y_140 140 CAMK2A NM_015981 INTRON OMIM: 114078 CAMK2A, KIAA0968, CA Calcium/calmodulin-dependent protein kinase II-alpha MOUSE: 18(Camk2a) chr5_149649764_y_140 140 CAMK2A NM_171825 INTRON OMIM: 114078 CAMK2A, KIAA0968, CA Calcium/calmodulin-dependent protein kinase II-alpha MOUSE: 18(Camk2a) chr7_101646716_y_140 140 C7orf19 NM_032831 INTRON chr7_70198933_y_140 140 WBSCR17 NM_022479 INTRON chr8_113752202_r_140 140 CSMD3 NM_052900 INTRON OMIM: 608399 CSMD3, KIAA1894 Cub and Sushi multiple domains 3 chr8_17067476_y_140 140 ZDHHC2 NM_016353 INTRON chr8_4765772_r_140 140 CSMD1 NM_033225 INTRON OMIM: 608397 CSMD1, KIAA1890 Cub and Sushi multiple domains 1 chrX_134515072_y_140 140 ARHGEF6 NM_004840 INTRON OMIM: 300267 ARHGEF6, MRX46, COOL Rho guanine nucleotide exchange factor-6 Mental retardation, X-linked nonspecific, type 46, 300436 (3) chr10_11242928_r_141 141 CUGBP2 NM_006561 INTRON chr10_113724576_r_141 141 TECTB NM_058222 INTRON chr12_45897470_r_141 141 MGC16044 NM_138371 UTR chr14_90799965_y_141 141 SLC24A4 NM_153648 INTRON chr14_90799965_y_141 141 SLC24A4 NM_153646 INTRON chr14_90799965_y_141 141 SLC24A4 NM_153647 INTRON chr16_7322940_y_141 141 A2BP1 NM_018723 INTRON chr16_74356132_r_141 141 GLG1 NM_012201 INTRON OMIM: 600753 GLG1 Golgi apparatus protein 1 MOUSE: 8(Glg1) chr17_28873884_y_141 141 CPD NM_001304 INTRON OMIM: 603102 CPD Carboxypeptidase D MOUSE: 11(Cpd) chr18_70391239_r_141 141 CPGL2 NM_032649 INTRON chr19_8532234_y_141 141 MYO1F NM_012335 INTRON OMIM: 601480 MYO1F Myosin IF MOUSE: 17(Myo1f) chr1_166506767_r_141 141 NME7 NM_013330 INTRON chr1_18939064_r_141 141 RBAF600 NM_020765 INTRON chr20_52531819_r_141 141 FLJ33887 NM_173485 INTRON chr21_30160584_r_141 141 GRIK1 NM_175611 INTRON OMIM: 138245 GRIK1, GLUR5 Glutamate receptor, ionotropic, kainate 1 MOUSE: 16(Glur5) chr21_30160584_r_141 141 GRIK1 NM_000830 INTRON OMIM: 138245 GRIK1, GLUR5 Glutamate receptor, ionotropic, kainate 1 MOUSE: 16(Glur5) chr2_17786980_y_141 141 VSNL1 NM_003385 INTRON OMIM: 600817 VSNL1 Visinin-like 1 chr2_212763238_y_141 141 ERBB4 NM_005235 INTRON OMIM: 600543 ERBB4, HER4 Avian erythroblastic leukemia viral (v-erb-b2) oncogene homolog 4 chr2_50575254_r_141 141 NRXN1 NM_004801 INTRON OMIM: 600565 NRXN1 Neurexin 1 chr2_70103851_y_141 141 RY1 NM_006857 INTRON OMIM: 600515 P2RY12, P2Y12 Purinergic receptor P2Y, G protein-coupled, 12 Platelet ADP receptor defect (3) chr3_13885779_r_141 141 WNT7A NM_004625 INTRON OMIM: 601570 WNT7A Wingless-type MMTV integration site family, member 7A chr3_186703871_r_141 141 IMP-2 NM_006548 INTRON chr4_70808757_r_141 141 UGT2A1 NM_006798 INTRON OMIM: 604716 UGT2A1 Uridine diphosphate glycosyltransferase 2 family, member A1 chr5_156452482_r_141 141 HAVCR1 NM_012206 INTRON OMIM: 606518 HAVCR1, HAVCR Hepatitis A virus cellular receptor 1 chr5_64587050_r_141 141 ADAMTS6 NM_014273 INTRON OMIM: 605008 ADAMTS6 A disintegrin-like and metalloproteinase with thrombospondin type 1motif, 6 chr5_77531906_y_141 141 AP3B1 NM_003664 INTRON OMIM: 603401 AP3B1, ADTB3A, HPS2 Adaptor-related protein complex 3, beta 1 subunit (adaptin, beta-3a) Hermansky-Pudlak syndrome, 608233 (3) MOUSE: 13(Ap3bi, pe) chr7_107457980_r_141 141 NRCAM NM_005010 UTR OMIM: 601581 NRCAM Neuronal cell adhesion molecule chr9_110374022_r_141 141 ROD1 NM_005156 INTRON OMIM: 601724 NEUROD1, NIDDM Neurogenic differentiation 1 {Diabetes mellitus, noninsulin-dependent}, 125853 (3) MOUSE: 2(Neurod) chr9_114929254_r_141 141 ASTN2 NM_014010 INTRON chr9_34006209_r_141 141 UBAP2 NM_018449 INTRON chr9_34006209_r_141 141 UBAP2 NM_020867 INTRON chr9_34006209_r_141 141 UBAP2 NM_148171 INTRON chr9_34210009_y_141 141 UBAP1 NM_016525 UTR chrX_127942452_r_141 141 RAB33A NM_004794 UTR OMIM: 300333 RAB33A Ras-associated protein RAB33A chrX_127942452_r_141 141 ELF4 NM_001421 UTR chrX_90358119_y_141 141 PCDH11X NM_032968 INTRON OMIM: 300246 PCDH11X, PCDH11, PCD Protocadherin 11, X-linked chrX_90358119_y_141 141 PCDH11X NM_032969 INTRON OMIM: 300246 PCDH11X, PCDH11, PCD Protocadherin 11, X-linked chrX_9912854_r_141 141 MID1 NM_000381 INTRON OMIM: 300000 MID1, OGS1, BBBG1, F Midline-1 type II defect on chr.22 Opitz G syndrome, type I (3) MOUSE: X(Mid1) chrX_9912854_r_141 141 MID1 NM_033291 INTRON OMIM: 300000 MID1, OGS1, BBBG1, F Midline-1 type II defect on chr.22 Opitz G syndrome, type I (3) MOUSE: X(Mid1) chrX_9912854_r_141 141 MID1 NM_033290 INTRON OMIM: 300000 MID1, OGS1, BBBG1, F Midline-1 type II defect on chr.22 Opitz G syndrome, type I (3) MOUSE: X(Mid1) chr10_12136364_y_142 142 KIAA1630 NM_018706 INTRON chr11_119682379_r_142 142 POU2F3 NM_014352 INTRON OMIM: 607394 POU2F3, OCT11 POU domain, class 2, transcription factor 3 MOUSE: 9(Oct11) chr11_75931982_y_142 142 C11ORF30 NM_020193 INTRON chr12_3699610_r_142 142 MGC4266 NM_032680 UTR chr13_19085015_y_142 142 IL17D NM_138284 INTRON OMIM: 607587 IL17D Interleukin 17D ?associated with Hodgkin lymphoma chr14_63462193_y_142 142 FNTB NM_002028 INTRON OMIM: 134636 FNTB Farnesyltransferase, CAAX box, beta related FNTBL1 on 9 chr16_19468739_y_142 142 TMC5 NM_024780 INTRON chr16_56945237_r_142 142 CPNE2 NM_152727 INTRON chr16_61577413_y_142 142 CDH8 NM_001796 INTRON OMIM: 603580 PCDH8 Protocadherin 8 MOUSE: 14(Pcdh8) chr17_62063919_r_142 142 ACE NM_152831 UTR OMIM: 608192 PACE1 Protein associated with the C-terminal domain of ezrin chr19_41797603_y_142 142 ZNF382 NM_032825 INTRON chr19_63165046_y_142 142 MGC41906 NM_152474 INTRON chr19_7143184_r_142 142 INSR NM_000208 INTRON OMIM: 147671 INSRR, IRR Insulin receptor-related receptor chr1_234720093_y_142 142 RYR2 NM_001035 INTRON OMIM: 180902 RYR2, VTSIP Ryanodine receptor-2 (cardiac) Ventricular tachycardia, stress-induced polymorphic, 604772 (3);Arrhythmogenic r MOUSE: 13(Ryr2) chr2_170358105_r_142 142 LRP2 NM_004525 INTRON OMIM: 600073 LRP2 Low density lipoprotein-related protein 2 chr3_99878843_y_142 142 ESDN NM_080927 INTRON chr4_102504215_r_142 142 PPP3CA NM_000944 INTRON OMIM: 114105 PPP3CA, PPP2B, CALNA Protein phosphatase-3 (formerly 2B), catalytic subunit, alpha isoform(calcineuri chr4_124224491_y_142 142 FGF2 NM_002006 INTRON OMIM: 134920 FGF2, FGFB Fibroblast growth factor-2 (basic) many alternate names MOUSE: 3(Fgf2) chr4_20658511_y_142 142 KCNIP4 NM_147183 INTRON OMIM: 608182 KCNIP4, KCHIP4 Kv channel-interacting protein 4 chr4_20658511_y_142 142 KCNIP4 NM_147182 UTR OMIM: 608182 KCNIP4, KCHIP4 Kv channel-interacting protein 4 chr4_22554118_y_142 142 GBA3 NM_020973 INTRON chr5_175498091_r_142 142 NY-REN-7 NM_173663 INTRON chr5_52793930_y_142 142 FST NM_006350 INTRON OMIM: 136470 FST, FS Follistatin Polycystic ovary syndrome, 184700 (2) chr5_52793930_y_142 142 FST NM_013409 INTRON OMIM: 136470 FST, FS Follistatin Polycystic ovary syndrome, 184700 (2) chr5_64631370_r_142 142 ADAMTS6 NM_014273 INTRON OMIM: 605008 ADAMTS6 A disintegrin-like and metalloproteinase with thrombospondin type 1motif, 6 chr6_108760803_y_142 142 LACE1 NM_145315 INTRON chr6_157391741_y_142 142 ELD/OSA1 NM_175863 INTRON chr6_157391741_y_142 142 ELD/OSA1 NM_020732 INTRON chr6_163182220_r_142 142 PACRG NM_152410 INTRON chr7_16664421_y_142 142 BCMP11 NM_176813 UTR chr8_113533087_y_142 142 CSMD3 NM_052900 INTRON OMIM: 608399 CSMD3, KIAA1894 Cub and Sushi multiple domains 3 chr8_113815069_y_142 142 CSMD3 NM_052900 INTRON OMIM: 608399 CSMD3, KIAA1894 Cub and Sushi multiple domains 3 chr8_119065420_r_142 142 EXT1 NM_000127 INTRON OMIM: 608177 EXT1 Exostosin 1 distal to TRPS1 Exostoses, multiple, type 1, 133700 (3); Chondrosarcoma, 215300 (3) MOUSE: 15(Ext1) chr8_30464912_y_142 142 RBPMS NM_006867 INTRON chr8_40756273_r_142 142 FLJ13842 NM_024645 UTR chr10_108489743_y_143 143 SORCS1 NM_052918 INTRON OMIM: 606283 SORCS1 SORCS receptor 1 chr10_132558109_r_143 143 LOC256536 NM_174937 INTRON chr10_15105056_y_143 143 FLJ11106 NM_018324 INTRON chr10_22203881_r_143 143 DNAJC1 NM_022365 INTRON chr12_80262210_y_143 143 PPFIA2 NM_003625 INTRON chr12_98035443_y_143 143 EB-1 NM_152788 UTR chr12_98035443_y_143 143 EB-1 NM_020140 INTRON chr14_71318420_r_143 143 DPF3 NM_012074 INTRON chr16_1236897_r_143 143 TPSG1 NM_012467 UTR chr1_39026176_y_143 143 MACF1 NM_012090 INTRON chr1_99784772_y_143 143 AGL NM_000642 INTRON OMIM: 232400 AGL, GDE Amylo-1,6-glucosidase, 4-alpha-glucanotransferase (glycogendebranching enzyme) Glycogen storage disease IIIa (3); Glycogen storage disease IIIb (3) chr1_99784772_y_143 143 AGL NM_000028 INTRON OMIM: 232400 AGL, GDE Amylo-1,6-glucosidase, 4-alpha-glucanotransferase (glycogendebranching enzyme) Glycogen storage disease IIIa (3); Glycogen storage disease IIIb (3) chr1_99784772_y_143 143 AGL NM_000643 INTRON OMIM: 232400 AGL, GDE Amylo-1,6-glucosidase, 4-alpha-glucanotransferase (glycogendebranching enzyme) Glycogen storage disease IIIa (3); Glycogen storage disease IIIb (3) chr1_99784772_y_143 143 AGL NM_000644 INTRON OMIM: 232400 AGL, GDE Amylo-1,6-glucosidase, 4-alpha-glucanotransferase (glycogendebranching enzyme) Glycogen storage disease IIIa (3); Glycogen storage disease IIIb (3) chr1_99784772_y_143 143 AGL NM_000646 INTRON OMIM: 232400 AGL, GDE Amylo-1,6-glucosidase, 4-alpha-glucanotransferase (glycogendebranching enzyme) Glycogen storage disease IIIa (3); Glycogen storage disease IIIb (3) chr20_13551902_r_143 143 C20orf13 NM_017714 INTRON chr20_43590402_r_143 143 GDAP1L1 NM_024034 INTRON chr20_59228279_y_143 143 CDH26 NM_177980 INTRON chr22_35717977_r_143 143 TMPRSS6 NM_153609 INTRON chr2_15715628_y_143 143 NAG NM_015909 UTR OMIM: 606828 NAGK, GNK N-acetylglucosamine kinase chr2_74527494_r_143 143 SLC4A5 NM_133478 UTR OMIM: 606757 SLC4A5, NBC4 Solute carrier family 4, sodium bicarbonate cotransporter, member 5 chr2_74527494_r_143 143 SLC4A5 NM_133479 UTR OMIM: 606757 SLC4A5, NBC4 Solute carrier family 4, sodium bicarbonate cotransporter, member 5 chr2_74527494_r_143 143 SLC4A5 NM_033323 UTR OMIM: 606757 SLC4A5, NBC4 Solute carrier family 4, sodium bicarbonate cotransporter, member 5 chr2_84755002_y_143 143 FLJ37357 NM_173645 INTRON chr4_15757312_y_143 143 PROM1 NM_006017 INTRON OMIM: 604365 PROM1, PROML1, AC133 Prominin 1 Retinal degeneration, autosomal recessive, prominin-related (3) chr4_96720998_r_143 143 UNC5C NM_003728 INTRON OMIM: 603610 UNC5C, UNC5H3 UNC5, C. elegans, homolog of, C MOUSE: 3(Unc5c) chr7_27830851_y_143 143 JAZF1 NM_175061 INTRON OMIM: 606246 JAZF1 JAZF1 gene Endometrial stromal tumors (2) chr8_131815392_y_143 143 ADCY8 NM_001115 INTRON OMIM: 103070 ADCY8, ADCY3 Adenylyl cyclase-8, brain chr8_13347642_r_143 143 DLC1 NM_182643 INTRON OMIM: 604050 DLEC1, DLC1 Deleted in lung and esophageal cancer 1 Lung cancer, 211980 (1); Esophageal cancer, 133239 (1) chr8_13347642_r_143 143 DLC1 NM_024767 INTRON OMIM: 604050 DLEC1, DLC1 Deleted in lung and esophageal cancer 1 Lung cancer, 211980 (1); Esophageal cancer, 133239 (1) chr8_17743262_y_143 143 FGL1 NM_147203 INTRON OMIM: 605776 FGL1, HFREP1 Fibrinogen-like 1 chr8_17743262_y_143 143 FGL1 NM_004467 INTRON OMIM: 605776 FGL1, HFREP1 Fibrinogen-like 1 chr8_76428767_y_143 143 HNF4G NM_004133 UTR OMIM: 605966 HNF4G Hepatocyte nuclear factor 4-gamma MOUSE: 3(Hnf4g) chr9_83076010_r_143 143 NTRK2 NM_006180 INTRON OMIM: 600456 NTRK2, TRKB Neurotrophic tyrosine kinase, receptor, type 2 chr9_96351829_y_143 143 TBC1D2 NM_018421 INTRON chrX_14730284_y_143 143 FIGF NM_004469 INTRON OMIM: 300091 FIGF, VEGFD c-fos induced growth factor (vascular endothelial growth factor D) chr12_120802349_y_144 144 MGC33630 NM_144668 INTRON chr17_37971149_r_144 144 PPARBP NM_004774 INTRON OMIM: 604311 PPARBP, PBP, TRAP220 Peroxisome proliferator-activated receptor-binding protein chr17_49201626_r_144 144 ABCC3 NM_003786 INTRON OMIM: 604323 ABCC3, CMOAT2, MRP3, ATP-binding cassette, sub-family C, member 3 chr17_49201626_r_144 144 ABCC3 NM_020037 INTRON OMIM: 604323 ABCC3, CMOAT2, MRP3, ATP-binding cassette, sub-family C, member 3 chr17_49201626_r_144 144 ABCC3 NM_020038 INTRON OMIM: 604323 ABCC3, CMOAT2, MRP3, ATP-binding cassette, sub-family C, member 3 chr19_10556889_r_144 144 AP1M2 NM_005498 INTRON OMIM: 607309 AP1M2, MU1B Adaptor-related protein complex 1, mu-2 subunit MOUSE: 9(Ap1m2) chr19_59612053_r_144 144 ILT7 NM_012276 INTRON chr19_9872567_r_144 144 OLFM2 NM_058164 INTRON chr1_50354938_r_144 144 FAF1 NM_007051 INTRON chr1_50354938_r_144 144 FAF1 NM_131917 INTRON chr20_43241658_y_144 144 C20orf100 NM_032883 UTR chr21_30180896_y_144 144 GRIK1 NM_175611 INTRON OMIM: 138245 GRIK1, GLUR5 Glutamate receptor, ionotropic, kainate 1 MOUSE: 16(Glur5) chr21_30180896_y_144 144 GRIK1 NM_000830 INTRON OMIM: 138245 GRIK1, GLUR5 Glutamate receptor, ionotropic, kainate 1 MOUSE: 16(Glur5) chr21_43929245_r_144 144 HSF2BP NM_007031 INTRON OMIM: 604554 HSF2BP Heat-shock transcription factor 2-binding protein chr2_106307064_y_144 144 ECRG4 NM_032411 INTRON chr2_116525339_y_144 144 DPP10 NM_020868 INTRON chr3_2497691_y_144 144 CNTN4 NM_175607 UTR OMIM: 607280 CNTN4 Contactin 4 chr3_36400516_r_144 144 STAC NM_003149 INTRON OMIM: 602317 STAC SRC homology three (SH3) and cysteine-rich domain MOUSE: 9(Stac) chr4_5918132_r_144 144 CRMP1 NM_001313 INTRON OMIM: 602462 CRMP1, DPYSL1, DRP1 Collapsin response mediator protein-1 chr5_65005018_r_144 144 SGT2 NM_019072 INTRON chr6_149344658_y_144 144 UST NM_005715 INTRON OMIM: 604318 GTF2IRD1, GTF3, MUST GTF21 repeat domain-containing protein 1 chr6_53979647_y_144 144 C6orf142 NM_138569 INTRON chr7_158068421_y_144 144 FLJ10300 NM_018051 UTR chr8_70734715_r_144 144 SLC21A15 NM_030958 INTRON chr10_27979272_r_145 145 MGC39616 NM_173576 INTRON chr16_67877153_y_145 145 FLJ20399 NM_017803 INTRON chr17_31734882_r_145 145 ACCN1 NM_001094 INTRON OMIM: 601784 ACCN1, BNC1, MDEG Amiloride-sensitive cation channel 1, neuronal (degenerin) chr18_10452557_y_145 145 APCDD1 NM_153000 INTRON OMIM: 607479 APCDD1 Adenomatosis polyposis coli down-regulated 1 chr19_16000827_r_145 145 FLJ25328 NM_152483 UTR chr19_53470211_r_145 145 MGC17986 NM_153608 UTR chr19_54359254_y_145 145 TRPM4 NM_017636 INTRON OMIM: 606936 TRPM4 Transient receptor potential cation channel, subfamily M, member 4 chr19_7408862_y_145 145 P114-RHO-GEF NM_015318 UTR chr1_152485534_y_145 145 PKLR NM_181871 INTRON OMIM: 266200 PKLR, PK1 Pyruvate kinase, liver and RBC type Anemia, hemolytic, due to PK deficiency (3) MOUSE: 3(Pk1) chr1_152485534_y_145 145 PKLR NM_000298 INTRON OMIM: 266200 PKLR, PK1 Pyruvate kinase, liver and RBC type Anemia, hemolytic, due to PK deficiency (3) MOUSE: 3(Pk1) chr1_234769532_y_145 145 RYR2 NM_001035 INTRON OMIM: 180902 RYR2, VTSIP Ryanodine receptor-2 (cardiac) Ventricular tachycardia, stress-induced polymorphic, 604772 (3);Arrhythmogenic r MOUSE: 13(Ryr2) chr1_2858194_y_145 145 PRDM16 NM_022114 INTRON OMIM: 605557 PRDM16, MEL1 PR domain-containing protein 16 chr1_50753158_r_145 145 FAF1 NM_007051 INTRON chr1_50753158_r_145 145 FAF1 NM_131917 INTRON chr1_99994027_y_145 145 HIAT1 NM_033055 INTRON chr20_4203292_y_145 145 ADRA1D NM_000678 INTRON OMIM: 104219 ADRA1D, ADRA1A Adrenergic, alpha-1D-, receptor incorrectly assigned to 5q MOUSE: 11(Adra1a) chr2_111795957_r_145 145 FLJ11042 NM_018308 INTRON chr2_112823462_y_145 145 MERTK NM_006343 INTRON OMIM: 604705 MERTK Mer tyrosine kinase protooncogene Retinitis pigmentosa, MERTK-related, 268000 (3) chr2_115334588_r_145 145 DPP10 NM_020868 INTRON chr2_50752670_r_145 145 NRXN1 NM_004801 INTRON OMIM: 600565 NRXN1 Neurexin 1 chr2_98180822_r_145 145 PRO1048 NM_018497 UTR chr3_21650701_r_145 145 FLJ22419 NM_024697 INTRON chr3_24249935_r_145 145 THRB NM_000461 UTR OMIM: 190160 THRB, ERBA2, THR1 Thyroid hormone receptor, beta (avian erythroblastic leukemia viral(v-erb-a) onc Thyroid hormone resistance, 274300, 188570 (3) chr7_145374668_y_145 145 CNTNAP2 NM_014141 INTRON OMIM: 604569 CNTNAP2, CASPR2, NRX Contactin-associated protein-like 2 chr8_133721581_r_145 145 FLJ33069 NM_144649 INTRON chr8_55054006_r_145 145 LYPLA1 NM_006330 INTRON OMIM: 605599 LYPLA1 Lysophospholipase I chr9_103493651_r_145 145 CDW92 NM_080546 INTRON chr9_103493651_r_145 145 CDW92 NM_022109 INTRON chr9_131857277_y_145 145 DBH NM_000787 INTRON OMIM: 223360 DBH Dopamine-beta-hydroxylase tightly linked to ABO [Dopamine-beta-hydroxylase activity levels, plasma] (3) MOUSE: 2(Dbh) chrY_4944035_y_145 145 PCDH11Y NM_032973 INTRON OMIM: 400022 PCDH11Y, PCDH22, PCD Protocadherin 22 chr11_106851137_r_146 146 FLJ32343 NM_152434 UTR chr11_59377056_y_146 146 GIF NM_005142 INTRON OMIM: 261000 GIF Gastric intrinsic factor Anemia, pernicious, congenital, due to deficiency of intrinsicfactor (1) MOUSE: 19(Gif) chr12_49273736_y_146 146 FLJ34278 NM_173602 INTRON chr13_22651005_y_146 146 FLJ31208 NM_153023 INTRON chr15_25618458_y_146 146 OCA2 NM_000275 INTRON OMIM: 120436 MLH1, COCA2, HNPCC2 mutL, E. coli, homolog of, 1 Colorectal cancer, hereditary nonpolyposis, type 2, 114500 (3);Turcot syndrome w chr15_46425637_y_146 146 FBN1 NM_000138 INTRON OMIM: 134797 FBN1, MFS1 Fibrillin-1 Marfan syndrome, 154700 (3); Shprintzen-Goldberg syndrome,182212 (3); Ectopia le MOUSE: 2(Fbn1) chr17_46957374_y_146 146 SCAP1 NM_003726 INTRON OMIM: 604969 SCAP1, SKAP55 SRC kinase-associated phosphoprotein 1, 55kD chr19_6783630_y_146 146 TRIP10 NM_004240 UTR chr19_6783630_y_146 146 VAV1 NM_005428 INTRON OMIM: 164875 VAV1, VAV Oncogene VAV1 close to INSR chr1_116918133_r_146 146 IGSF2 NM_004258 INTRON chr1_11943725_y_146 146 TNFRSF1B NM_001066 INTRON OMIM: 191191 TNFRSF1B, TNFR2, TNF Tumor necrosis factor receptor superfamily, member 1B MOUSE: 4(Tnfr1) chr1_213607646_r_146 146 USH2A NM_007123 INTRON OMIM: 608400 USH2A Usherin unlinked = USH2B Usher syndrome, type 2A, 276901 (3); Retinitis pigmentosa, AR,without hearing lo MOUSE: 1(Ush2a) chr1_39066849_y_146 146 MACF1 NM_012090 INTRON chr1_59881758_y_146 146 MGC34837 NM_152377 INTRON chr2_128423311_y_146 146 PROC NM_000312 UTR OMIM: 176860 PROC Protein C (inactivator of coagulation factors Va and VIIIa) Thrombophilia due to protein C deficiency (3); Purpura fulminans,neonatal (1) chr3_137604791_r_146 146 STAG1 NM_005862 INTRON chr3_95083280_y_146 146 DKFZp761H079 NM_144996 UTR chr5_19595300_r_146 146 CDH18 NM_004934 INTRON OMIM: 608287 PCDH18, KIAA1562 Protocadherin 18 chr6_129507738_r_146 146 LAMA2 NM_000426 INTRON OMIM: 156225 LAMA2, LAMM Laminin, alpha-2 (merosin) Muscular dystrophy, congenital merosin-deficient, 607855 (3);Muscular dystrophy, MOUSE: 10(dy, Lamm) chr7_139012048_y_146 146 TBXAS1 NM_001061 INTRON OMIM: 274180 TBXAS1 Thromboxane A synthase 1, platelet Thromboxane synthase deficiency (2) MOUSE: 6(Tbxas1) chr7_139012048_y_146 146 TBXAS1 NM_030984 INTRON OMIM: 274180 TBXAS1 Thromboxane A synthase 1, platelet Thromboxane synthase deficiency (2) MOUSE: 6(Tbxas1) chr8_106502568_y_146 146 ZFPM2 NM_012082 INTRON OMIM: 603693 ZFPM2, FOG2 Zinc finger protein, multitype 2 (friend of GATA2) chr8_70602263_r_146 146 SULF1 NM_015170 INTRON chr9_67730249_y_146 146 APBA1 NM_001163 UTR OMIM: 602414 APBA1, X11 Amyloid beta A4 precursor protein-binding, family A, member 1 chrX_16019273_r_146 146 CTPS2 NM_175859 INTRON OMIM: 300380 CTPS2 Cytidine 5-prime triphosphate synthetase 2 chrX_16019273_r_146 146 CTPS2 NM_019857 INTRON OMIM: 300380 CTPS2 Cytidine 5-prime triphosphate synthetase 2 chrX_84573176_y_146 146 DACH2 NM_053281 INTRON chr10_18160231_y_147 147 MRC1 NM_002438 INTRON OMIM: 153618 MRC1 Mannose receptor, C type 1 MOUSE: 2(Mrc1) chr11_98609770_y_147 147 CNTN5 NM_014361 UTR OMIM: 607219 CNTN5, NB2 Contactin 5 chr11_98609770_y_147 147 CNTN5 NM_175566 UTR OMIM: 607219 CNTN5, NB2 Contactin 5 chr12_46551314_y_147 147 VDR NM_000376 INTRON OMIM: 601769 VDR Vitamin D (1,25-dihydroxyvitamin D3) receptor Rickets, vitamin D-resistant, type IIA, 277440 (3); Rickets, vitaminD-resistant, chr13_26449137_r_147 147 FLT3 NM_004119 INTRON OMIM: 136351 FLT3 fms-related tyrosine kinase-3 Leukemia, acute myeloid, reduced survival in (3); Leukemia,acute myeloid (3) MOUSE: 5(Flt3) chr17_41600101_r_147 147 BRCA1 NM_007295 INTRON OMIM: 113705 BRCA1, PSCP Breast cancer-1 gene Breast cancer-1 (3); Ovarian cancer (3); Breast-ovarian cancer (3);Papillary ser MOUSE: 11(Brca1) chr17_41600101_r_147 147 BRCA1 NM_007294 INTRON OMIM: 113705 BRCA1, PSCP Breast cancer-1 gene Breast cancer-1 (3); Ovarian cancer (3); Breast-ovarian cancer (3);Papillary ser MOUSE: 11(Brca1) chr17_41600101_r_147 147 BRCA1 NM_007296 INTRON OMIM: 113705 BRCA1, PSCP Breast cancer-1 gene Breast cancer-1 (3); Ovarian cancer (3); Breast-ovarian cancer (3);Papillary ser MOUSE: 11(Brca1) chr17_41600101_r_147 147 BRCA1 NM_007297 INTRON OMIM: 113705 BRCA1, PSCP Breast cancer-1 gene Breast cancer-1 (3); Ovarian cancer (3); Breast-ovarian cancer (3);Papillary ser MOUSE: 11(Brca1) chr17_41600101_r_147 147 BRCA1 NM_007298 INTRON OMIM: 113705 BRCA1, PSCP Breast cancer-1 gene Breast cancer-1 (3); Ovarian cancer (3); Breast-ovarian cancer (3);Papillary ser MOUSE: 11(Brca1) chr17_41600101_r_147 147 BRCA1 NM_007299 INTRON OMIM: 113705 BRCA1, PSCP Breast cancer-1 gene Breast cancer-1 (3); Ovarian cancer (3); Breast-ovarian cancer (3);Papillary ser MOUSE: 11(Brca1) chr17_41600101_r_147 147 BRCA1 NM_007300 INTRON OMIM: 113705 BRCA1, PSCP Breast cancer-1 gene Breast cancer-1 (3); Ovarian cancer (3); Breast-ovarian cancer (3);Papillary ser MOUSE: 11(Brca1) chr17_41600101_r_147 147 BRCA1 NM_007301 INTRON OMIM: 113705 BRCA1, PSCP Breast cancer-1 gene Breast cancer-1 (3); Ovarian cancer (3); Breast-ovarian cancer (3);Papillary ser MOUSE: 11(Brca1) chr17_41600101_r_147 147 BRCA1 NM_007302 INTRON OMIM: 113705 BRCA1, PSCP Breast cancer-1 gene Breast cancer-1 (3); Ovarian cancer (3); Breast-ovarian cancer (3);Papillary ser MOUSE: 11(Brca1) chr17_41600101_r_147 147 BRCA1 NM_007303 INTRON OMIM: 113705 BRCA1, PSCP Breast cancer-1 gene Breast cancer-1 (3); Ovarian cancer (3); Breast-ovarian cancer (3);Papillary ser MOUSE: 11(Brca1) chr17_41600101_r_147 147 BRCA1 NM_007304 INTRON OMIM: 113705 BRCA1, PSCP Breast cancer-1 gene Breast cancer-1 (3); Ovarian cancer (3); Breast-ovarian cancer (3);Papillary ser MOUSE: 11(Brca1) chr17_41600101_r_147 147 BRCA1 NM_007305 INTRON OMIM: 113705 BRCA1, PSCP Breast cancer-1 gene Breast cancer-1 (3); Ovarian cancer (3); Breast-ovarian cancer (3);Papillary ser MOUSE: 11(Brca1) chr17_41600101_r_147 147 BRCA1 NM_007306 UTR OMIM: 113705 BRCA1, PSCP Breast cancer-1 gene Breast cancer-1 (3); Ovarian cancer (3); Breast-ovarian cancer (3);Papillary ser MOUSE: 11(Brca1) chr19_53218326_r_147 147 ELSPBP1 NM_022142 UTR chr1_143156774_r_147 147 LOC64182 NM_022359 UTR chr1_229057484_y_147 147 DISC1 NM_018662 INTRON OMIM: 605210 DISC1 Disrupted in schizophrenia 1 Schizophrenia, 181500 (2) MOUSE: 8(Disc1) chr20_18671068_y_147 147 HARS2 NM_080820 INTRON chr2_10842138_r_147 147 FLJ14075 NM_024894 INTRON chr2_116534429_y_147 147 DPP10 NM_020868 INTRON chr2_212906385_r_147 147 ERBB4 NM_005235 INTRON OMIM: 600543 ERBB4, HER4 Avian erythroblastic leukemia viral (v-erb-b2) oncogene homolog 4 chr2_217141695_r_147 147 PECR NM_018441 INTRON chr4_147377382_r_147 147 LOC152485 NM_178835 INTRON chr4_152157409_y_147 147 LRBA NM_006726 INTRON chr4_170326549_r_147 147 KIAA0992 NM_016081 INTRON OMIM: 608092 KIAA0992 Palladin, mouse, homolog of chr5_140755052_y_147 147 PCDHGA1 NM_018912 INTRON OMIM: 606288 PCDHGA1 Protocadherin-gamma, subfamily A, member 1 chr5_140755052_y_147 147 PCDHGA2 NM_018915 INTRON OMIM: 606289 PCDHGA2 Protocadherin-gamma, subfamily A, member 2 chr5_140755052_y_147 147 PCDHGA3 NM_018916 INTRON OMIM: 606290 PCDHGA3 Protocadherin-gamma, subfamily A, member 3 chr5_146471027_r_147 147 PPP2R2B NM_181677 UTR OMIM: 604325 PPP2R2B Protein phosphatase 2, regulatory subunit B, beta Spinocerebellar ataxia 12, 604326 (3) chr5_146471027_r_147 147 PPP2R2B NM_181678 UTR OMIM: 604325 PPP2R2B Protein phosphatase 2, regulatory subunit B, beta Spinocerebellar ataxia 12, 604326 (3) chr8_97895329_y_147 147 PGCP NM_016134 INTRON chrX_10197038_y_147 147 MID1 NM_033290 UTR OMIM: 300000 MID1, OGS1, BBBG1, F Midline-1 type II defect on chr.22 Opitz G syndrome, type I (3) MOUSE: X(Mid1) chrX_133776173_y_147 147 SLC9A6 NM_006359 INTRON OMIM: 300231 SLC9A6, NHE6 Solute carrier family 9 (sodium/hydrogen exchanger), isoform 6 chrX_5400525_y_147 147 NLGN4 NM_020742 INTRON OMIM: 300427 NLGN4, KIAA1260 Neuroligin 4 Autism, X-linked, 300425 (3); Asperger syndrome, 300425 (3) chrX_5400525_y_147 147 NLGN4 NM_181332 INTRON OMIM: 300427 NLGN4, KIAA1260 Neuroligin 4 Autism, X-linked, 300425 (3); Asperger syndrome, 300425 (3) chr10_102442131_r_148 148 FLJ23209 NM_024895 INTRON chr10_134358166_y_148 148 GPR123 NM_032422 INTRON chr11_19930442_y_148 148 NAV2 NM_145117 INTRON OMIM: 607026 NAV2, RAINB1, KIAA14 Neuron navigator 2 chr12_24881203_r_148 148 BCAT1 NM_005504 INTRON OMIM: 113520 BCAT1, BCT1 Branched chain aminotransferase-1, cytosolic ?Hyperleucinemia-isoleucinemia or hypervalinemia (1) MOUSE: 6(Bcat1) chr14_66882690_y_148 148 RAD51L1 NM_133510 INTRON OMIM: 602948 RAD51L1 RAD51. S. cerevisiae, homolog of, like 1 chr14_66882690_y_148 148 RAD51L1 NM_002877 INTRON OMIM: 602948 RAD51L1 RAD51. S. cerevisiae, homolog of, like 1 chr14_66882690_y_148 148 RAD51L1 NM_133509 INTRON OMIM: 602948 RAD51L1 RAD51. S. cerevisiae, homolog of, like 1 chr17_33588436_r_148 148 RAD51L3 NM_002878 INTRON OMIM: 602954 RAD51L3, RAD51D RAD51, S. cerevisiae, homolog of, D MOUSE: 11(Rad51d) chr17_33588436_r_148 148 RAD51L3 NM_133627 INTRON OMIM: 602954 RAD51L3, RAD51D RAD51, S. cerevisiae, homolog of, D MOUSE: 11(Rad51d) chr17_33588436_r_148 148 RAD51L3 NM_133628 INTRON OMIM: 602954 RAD51L3, RAD51D RAD51, S. cerevisiae, homolog of, D MOUSE: 11(Rad51d) chr17_33588436_r_148 148 RAD51L3 NM_133629 INTRON OMIM: 602954 RAD51L3, RAD51D RAD51, S. cerevisiae, homolog of, D MOUSE: 11(Rad51d) chr17_33588436_r_148 148 RAD51L3 NM_133630 INTRON OMIM: 602954 RAD51L3, RAD51D RAD51, S. cerevisiae, homolog of, D MOUSE: 11(Rad51d) chr17_38496376_r_148 148 GSDM NM_178171 UTR chr1_154114998_y_148 148 FLJ32884 NM_144702 INTRON chr1_62111404_r_148 148 LOC163782 NM_181712 INTRON chr2_125522831_y_148 148 caspr5 NM_130773 INTRON chr2_125522831_y_148 148 caspr5 NM_138996 INTRON chr5_118535227_r_148 148 DMXL1 NM_005509 INTRON OMIM: 605671 DMXL1 DMX-like 1 chr5_169697486_y_148 148 LCP2 NM_005565 INTRON OMIM: 601603 LCP2, SLP76 Lymphocyte cytosolic protein-2 (SH2 domain-containing leukocyteprotein of 76kD) chr5_83540610_y_148 148 EDIL3 NM_005711 INTRON chr6_162041097_y_148 148 PARK2 NM_004562 INTRON OMIM: 602544 PRKN, PARK2, PDJ Parkin Parkinson disease, juvenile, type 2, 600116 (3); Adenocarcinoma oflung, somatic, MOUSE: 17(Park2) chr6_162041097_y_148 148 PARK2 NM_013987 INTRON OMIM: 602544 PRKN, PARK2, PDJ Parkin Parkinson disease, juvenile, type 2, 600116 (3); Adenocarcinoma oflung, somatic, MOUSE: 17(Park2) chr6_162041097_y_148 148 PARK2 NM_013988 INTRON OMIM: 602544 PRKN, PARK2, PDJ Parkin Parkinson disease, juvenile, type 2, 600116 (3); Adenocarcinoma oflung, somatic, MOUSE: 17(Park2) chr6_73646621_y_148 148 KCNQ5 NM_019842 INTRON OMIM: 607357 KCNQ5 Potassium channel, voltage-gated, KQT-like subfamily, member 5 chr7_106887334_y_148 148 SLC26A4 NM_000441 INTRON OMIM: 605646 SLC26A4, PDS, DFNB4 Solute carrier family 26 (sulfate transporter), member 4 3' and close to DRA Pendred syndrome, 274600 (3); Enlarged vestibular aqueduct, 603545(3); Deafness, chr7_44299305_y_148 148 NPC1L1 NM_013389 INTRON chr7_74836593_y_148 148 HIP1 NM_005338 UTR OMIM: 601767 HIP1 Huntingtin interacting protein-1 {Prostate cancer, progression of}, 176807 (1) MOUSE: 5(Hip1) chr8_4765913_r_148 148 CSMD1 NM_033225 INTRON OMIM: 608397 CSMD1, KIAA1890 Cub and Sushi multiple domains 1 chr8_51622837_r_148 148 SNTG1 NM_018967 INTRON chr11_19930857_y_149 149 NAV2 NM_145117 INTRON OMIM: 607026 NAV2, RAINB1, KIAA14 Neuron navigator 2 chr12_20951579_y_149 149 SLC21A8 NM_019844 INTRON chr15_76640313_y_149 149 CHRNB4 NM_000750 INTRON OMIM: 118509 CHRNB4 Cholinergic receptor, neuronal nicotinic, beta polypeptide-4 MOUSE: 9(Acrb4) chr19_46046686_r_149 149 CYP2A6 NM_000762 INTRON OMIM: 122720 CYP2A6, CYP2A3, CYP2 Cytochrome P450, subfamily IIA, phenobarbital-inducible, polypeptide6 Coumarin resistance, 122700 (3); {Nicotine addiction, protectionfrom} (3) MOUSE: 7(Cyp2a) chr1_209917775_r_149 149 SNFT NM_018664 INTRON chr2_11492600_r_149 149 ROCK2 NM_004850 INTRON OMIM: 604002 ROCK2 RHO-associated coiled-coil-containing protein kinase 2 chr2_236768365_y_149 149 CENTG2 NM_014914 INTRON chr3_187886881_r_149 149 APM1 NM_004797 UTR OMIM: 605441 APM1, GBP28 Adiponectin (gelatin-binding protein, 28kD) conflicting assignment 1q21.3-q23 Adiponectin deficiency (3) MOUSE: 16(Apm1) chr3_55013895_y_149 149 CACNA2D3 NM_018398 INTRON OMIM: 606399 CACNA2D3 Calcium channel, voltage-dependent, alpha-2/delta subunit 3 chr5_7642286_r_149 149 ADCY2 NM_020546 INTRON OMIM: 103071 ADCY2 Adenylyl cyclase-2, brain MOUSE: 13(Adcy2) chr6_129510330_r_149 149 LAMA2 NM_000426 INTRON OMIM: 156225 LAMA2, LAMM Laminin, alpha-2 (merosin) Muscular dystrophy, congenital merosin-deficient, 607855 (3);Muscular dystrophy, MOUSE: 10(dy, Lamm) chr8_41639980_y_149 149 ANK1 NM_000037 INTRON OMIM: 182900 ANK1, SPH2 Ankyrin-1, erythrocytic Spherocytosis-2 (3) MOUSE: 8(nb) chr8_41639980_y_149 149 ANK1 NM_020475 INTRON OMIM: 182900 ANK1, SPH2 Ankyrin-1, erythrocytic Spherocytosis-2 (3) MOUSE: 8(nb) chr8_41639980_y_149 149 ANK1 NM_020476 INTRON OMIM: 182900 ANK1, SPH2 Ankyrin-1, erythrocytic Spherocytosis-2 (3) MOUSE: 8(nb) chr8_41639980_y_149 149 ANK1 NM_020477 INTRON OMIM: 182900 ANK1, SPH2 Ankyrin-1, erythrocytic Spherocytosis-2 (3) MOUSE: 8(nb) chr9_131873323_y_149 149 SARDH NM_007101 INTRON OMIM: 604455 SARDH, SARD, SAR Sarcosine dehydrogenase [Sarcosinemia], 268900 (2) MOUSE: 2(sar) chrX_29950724_r_149 149 FLJ11577 NM_025159 UTR chrY_4943675_y_149 149 PCDH11Y NM_032973 INTRON OMIM: 400022 PCDH11Y, PCDH22, PCD Protocadherin 22 chr10_17913311_y_150 150 MRC1 NM_002438 INTRON OMIM: 153618 MRC1 Mannose receptor, C type 1 MOUSE: 2(Mrc1) chr12_1561549_r_150 150 MGC40195 NM_152441 INTRON chr13_26825130_y_150 150 FLT1 NM_002019 INTRON OMIM: 165070 FLT1 fms-related tyrosine kinase-1 (vascular endothelial growthfactor/vascular permea 150kb from FLT3 chr14_87870100_r_150 150 CHES1 NM_005197 UTR OMIM: 602628 CHES1 Checkpoint suppressor 1 chr15_98742193_y_150 150 MGC27091 NM_178842 INTRON chr16_23859819_y_150 150 PRKCB1 NM_002738 INTRON OMIM: 176970 PRKCB1, PKCB Protein kinase C, beta 1 polypeptide chr16_30532476_y_150 150 ITGAL NM_002209 INTRON OMIM: 153370 ITGAL, CD11A, LFA1A Integrin, alpha-L (antigen CD11A (p180), lymphocytefunction-associated antigen-1 MOUSE: 7(Ly15) chr18_50746805_y_150 150 SE57-1 NM_025214 INTRON chr19_19149434_r_150 150 MEF2B NM_005919 UTR OMIM: 600661 MEF2B MADS box transcription enhancer factor 2, polypeptide B (myocyteenhancer factor MOUSE: ?8(Mef2b) chr19_4164198_y_150 150 FLJ10374 NM_018074 UTR chr1_8743302_y_150 150 CA6 NM_001215 INTRON OMIM: 114780 CA6 Carbonic anhydrase VI chr22_25037347_r_150 150 SEZ6L NM_021115 INTRON OMIM: 607021 SEZ6L Seizure-related 6-like chr22_31156841_r_150 150 BPIL2 NM_174932 INTRON chr3_161993583_y_150 150 PP2CE NM_139245 UTR chr6_112557638_y_150 150 LAMA4 NM_002290 INTRON OMIM: 600133 LAMA4, LAMA3 Laminin, alpha-4 chr6_73755546_r_150 150 KCNQ5 NM_019842 INTRON OMIM: 607357 KCNQ5 Potassium channel, voltage-gated, KQT-like subfamily, member 5 chr8_14112000_y_150 150 SGCZ NM_139167 INTRON chr9_34172590_y_150 150 UBAP1 NM_016525 UTR chrX_115987872_r_150 150 KIAA1309 NM_033495 UTR chr10_98021590_y_151 151 PIK3AP1 NM_152309 INTRON chr11_58271635_r_151 151 GLYAT NM_005838 UTR OMIM: 607424 GLYAT, ACGNAT, CAT Glycine-N-acyltransferase chr12_55780660_r_151 151 STAT6 NM_003153 INTRON OMIM: 601512 STAT6 Signal transducer and activator of transcription-6, interleukin-4induced MOUSE: 10(Stat6) chr15_31344675_r_151 151 RYR3 NM_001036 INTRON OMIM: 180903 RYR3 Ryanodine receptor-3 MOUSE: 2(Ryr3) chr15_43675205_y_151 151 SQRDL NM_021199 INTRON chr18_54758081_y_151 151 FLJ10697 NM_018181 INTRON chr19_16920586_r_151 151 VIP NM_015692 INTRON OMIM: 192321 VIPR1 Vasoactive intestinal peptide receptor 1 incorrectly assigned to 2q37 MOUSE: 9(Vipr1) chr2_116237334_r_151 151 DPP10 NM_020868 INTRON chr2_182088639_y_151 151 UBE2E3 NM_006357 INTRON OMIM: 604151 UBE2E3, UBCH9 Ubiquitin-conjugating enzyme E2E 3 chr2_80198958_r_151 151 CTNNA2 NM_004389 INTRON OMIM: 114025 CTNNA2, CAPR, CTNR Catenin, alpha-2 (cadherin-associated protein, related) MOUSE: 6(Capr) chr3_38739843_y_151 151 SCN10A NM_006514 INTRON OMIM: 604427 SCN10A Sodium channel, voltage-gated, type X, alpha subunit chr4_102703651_r_151 151 PPP3CA NM_000944 INTRON OMIM: 114105 PPP3CA, PPP2B, CALNA Protein phosphatase-3 (formerly 2B), catalytic subunit, alpha isoform(calcineuri chr4_186293736_y_151 151 FLJ33167 NM_152683 INTRON chr5_146308549_y_151 151 PPP2R2B NM_181676 INTRON OMIM: 604325 PPP2R2B Protein phosphatase 2, regulatory subunit B, beta Spinocerebellar ataxia 12, 604326 (3) chr5_146308549_y_151 151 PPP2R2B NM_181674 UTR OMIM: 604325 PPP2R2B Protein phosphatase 2, regulatory subunit B, beta Spinocerebellar ataxia 12, 604326 (3) chr5_146308549_y_151 151 PPP2R2B NM_181677 INTRON OMIM: 604325 PPP2R2B Protein phosphatase 2, regulatory subunit B, beta Spinocerebellar ataxia 12, 604326 (3) chr5_146308549_y_151 151 PPP2R2B NM_181678 UTR OMIM: 604325 PPP2R2B Protein phosphatase 2, regulatory subunit B, beta Spinocerebellar ataxia 12, 604326 (3) chr6_62649729_r_151 151 SLM1 NM_152688 INTRON chr7_90269103_y_151 151 PFTK1 NM_012395 INTRON chr8_126273714_r_151 151 FLJ32440 NM_173685 INTRON chr8_6512555_r_151 151 ANGPT2 NM_001147 UTR OMIM: 601922 ANGPT2, ANG2 Angiopoietin 2 close to MCPH1 MOUSE: 8(Angpt2) chr9_110381850_r_151 151 ROD1 NM_005156 INTRON OMIM: 601724 NEUROD1, NIDDM Neurogenic differentiation 1 {Diabetes mellitus, noninsulin-dependent}, 125853 (3) MOUSE: 2(Neurod) chr9_18527877_r_151 151 ADAMTSL1 NM_139264 INTRON chr9_18527877_r_151 151 ADAMTSL1 NM_052866 INTRON chr9_18527877_r_151 151 ADAMTSL1 NM_139238 INTRON chrX_28460465_y_151 151 IL1RAPL1 NM_014271 INTRON chrX_84694327_r_151 151 DACH2 NM_053281 INTRON chr11_84151874_y_152 152 DLG2 NM_001364 INTRON OMIM: 603583 DLG2 Discs large, Drosophila, homolog of, 2(channel-associated protein of synapses, 1 chr12_62885693_r_152 152 FLJ32549 NM_152440 INTRON chr12_68312076_y_152 152 CCT2 NM_006431 UTR OMIM: 605139 CCT2, CCTB Chaperonin containing T-complex polypeptide 1, subunit 2 chr16_22796761_y_152 152 HS3ST2 NM_006043 INTRON OMIM: 604056 HS3ST2, 30ST2 Heparan sulfate D-glucosaminyl 3-0-sulfotransferase 2 MOUSE: 7(30st2) chr16_23310948_r_152 152 SCNN1B NM_000336 UTR OMIM: 600760 SCNN1B Sodium channel, nonvoltage-gated 1, beta Liddle syndrome, 177200 (3); Pseudohypoaldosteronism, type I, 264350(3) MOUSE: 7(Scnn1b) chr19_2612210_r_152 152 FLJ00058 NM_052847 UTR chr19_45122798_r_152 152 FCGBP NM_003890 INTRON chr1_42264753_y_152 152 MGC47816 NM_173642 INTRON chr1_64074643_r_152 152 MGC35130 NM_152489 INTRON chr2_175423766_r_152 152 CIR NM_004882 INTRON OMIM: 604592 TCIRG1, TIRC7, OC116 T-cell immune regulator 1 Osteopetrosis, recessive, 259700 (3) MOUSE: 19(oc) chr3_117200146_r_152 152 LSAMP NM_002338 INTRON OMIM: 603241 LSAMP, LAMP Limbic system-associated membrane protein MOUSE: 16(Lsamp) chr3_128765961_r_152 152 MGLL NM_007283 INTRON chr5_139238604_y_152 152 DKFZp761B0514 NM_032289 INTRON chr6_38692931_r_152 152 GLO1 NM_006708 INTRON OMIM: 138750 GLO1 Glyoxalase I ~3cM proximal to HLA MOUSE: 17(Glo1) chr6_6314390_r_152 152 FLJ33708 NM_173675 UTR chr7_16664000_y_152 152 BCMP11 NM_176813 UTR chr8_50901078_y_152 152 SNTG1 NM_018967 UTR chr11_72727602_r_153 153 P2RY6 NM_176796 UTR OMIM: 602451 P2RY6, P2Y6 Pyrimidinergic receptor P2Y, G protein-coupled, 6 chr11_72727602_r_153 153 P2RY6 NM_176797 UTR OMIM: 602451 P2RY6, P2Y6 Pyrimidinergic receptor P2Y, G protein-coupled, 6 chr11_72727602_r_153 153 P2RY6 NM_176798 UTR OMIM: 602451 P2RY6, P2Y6 Pyrimidinergic receptor P2Y, G protein-coupled, 6 chr11_72727602_r_153 153 P2RY6 NM_004154 UTR OMIM: 602451 P2RY6, P2Y6 Pyrimidinergic receptor P2Y, G protein-coupled, 6 chr12_21356158_r_153 153 SLC21A3 NM_021094 INTRON OMIM: 602883 SLC21A3, OATP Solute carrier family 21 (organic anion transporter), member 3 chr12_21356158_r_153 153 SLC21A3 NM_134431 INTRON OMIM: 602883 SLC21A3, OATP Solute carrier family 21 (organic anion transporter), member 3 chr12_21356158_r_153 153 SLC21A3 NM_005075 INTRON OMIM: 602883 SLC21A3, OATP Solute carrier family 21 (organic anion transporter), member 3 chr13_70120971_y_153 153 DACH NM_004392 INTRON OMIM: 603803 DACH Dachshund, Drosophila, homolog of MOUSE: 13(Dach) chr13_70120971_y_153 153 DACH NM_080759 INTRON OMIM: 603803 DACH Dachshund, Drosophila, homolog of MOUSE: 13(Dach) chr13_70120971_y_153 153 DACH NM_080760 INTRON OMIM: 603803 DACH Dachshund, Drosophila, homolog of MOUSE: 13(Dach) chr16_23960097_y_153 153 PRKCB1 NM_002738 INTRON OMIM: 176970 PRKCB1, PKCB Protein kinase C, beta 1 polypeptide chr16_58291967_y_153 153 CSNK2A2 NM_001896 UTR OMIM: 115442 CSNK2A2 Casein kinase-2, alpha-prime polypeptide MOUSE: 8(Csnk2a2) chr16_58291967_y_153 153 NDRG4 NM_020465 UTR chr17_65110163_y_153 153 PRKCA NM_002737 INTRON OMIM: 176960 PRKCA, PKCA Protein kinase C, alpha polypeptide cen-COL1A1-PKCA-GH1 Pituitary tumor, invasive (3) MOUSE: 11(Pkca) chr17_6594848_r_153 153 PITPNM3 NM_031220 INTRON chr19_9895231_r_153 153 OLFM2 NM_058164 INTRON chr1_21350784_y_153 153 ALPL NM_000478 INTRON OMIM: 171760 ALPL, HOPS, TNSALP Alkaline phosphatase, liver/bone/kidney Hypophosphatasia, infantile, 241500 (3); Hypophosphatasia, childhood,241510 (3); MOUSE: 4(Akp2) chr1_65204242_y_153 153 DNAJC6 NM_014787 INTRON OMIM: 608375 DNAJC6, DJC6, KIAA04 DNAJ, E. coli, homolog of, subfamily C, member 6 chr21_37160846_r_153 153 HLCS NM_000411 INTRON OMIM: 253270 HLCS, HCS Holocarboxylase synthetase Multiple carboxylase deficiency, biotin-responsive (3);Multiple carboxylase defi MOUSE: 16(Hlcs) chr2_31575427_r_153 153 XDH NM_000379 INTRON OMIM: 607633 XDH Xanthine dehydrogenase (xanthine oxidase) Xanthinuria, type I, 278300 (3) MOUSE: 17(Xd) chr2_69179884_r_153 153 AMP18 NM_019617 INTRON chr2_69179884_r_153 153 GDDR NM_182536 UTR chr2_69297922_r_153 153 TEM8 NM_018153 INTRON OMIM: 606410 TEM8, ATR Tumor endothelial marker 8 (anthrax toxin receptor) chr2_69297922_r_153 153 TEM8 NM_053034 INTRON OMIM: 606410 TEM8, ATR Tumor endothelial marker 8 (anthrax toxin receptor) chr2_69297922_r_153 153 TEM8 NM_032208 INTRON OMIM: 606410 TEM8, ATR Tumor endothelial marker 8 (anthrax toxin receptor) chr5_177288459_y_153 153 NY-REN-7 NM_173663 INTRON chr6_73646770_y_153 153 KCNQ5 NM_019842 INTRON OMIM: 607357 KCNQ5 Potassium channel, voltage-gated, KQT-like subfamily, member 5 chr8_113338744_r_153 153 CSMD3 NM_052900 INTRON OMIM: 608399 CSMD3, KIAA1894 Cub and Sushi multiple domains 3 chr9_37225434_y_153 153 FLJ22611 NM_032226 INTRON chr10_120715608_y_154 154 GPRK5 NM_005308 INTRON OMIM: 600870 GPRK5, GRK5 G protein-coupled receptor kinase-5 chr11_20760112_y_154 154 NELL1 NM_006157 INTRON OMIM: 602319 NELL1 Nel-like 1 chr11_2292296_r_154 154 PHEMX NM_139022 INTRON OMIM: 603853 PHEMX, TSSC6 Pan-hematopoietic expression gene not imprinted chr11_2292296_r_154 154 PHEMX NM_139023 INTRON OMIM: 603853 PHEMX, TSSC6 Pan-hematopoietic expression gene not imprinted chr11_2292296_r_154 154 PHEMX NM_005705 INTRON OMIM: 603853 PHEMX, TSSC6 Pan-hematopoietic expression gene not imprinted chr11_2292296_r_154 154 PHEMX NM_139024 INTRON OMIM: 603853 PHEMX, TSSC6 Pan-hematopoietic expression gene not imprinted chr12_119680122_r_154 154 SPPL3 NM_139015 INTRON chr16_7071730_y_154 154 A2BP1 NM_018723 UTR chr17_16424208_r_154 154 PIGL NM_004278 INTRON OMIM: 605947 PIGL Phosphatidylinositol glycan, class L chr17_45162314_y_154 154 NSF NM_006178 INTRON OMIM: 601633 NSF N-ethylmaleimide-sensitive factor MOUSE: 11(Nsf) chr18_19721546_r_154 154 LAMA3 NM_000227 INTRON OMIM: 600133 LAMA4, LAMA3 Laminin, alpha-4 chr19_52921531_y_154 154 EHD2 NM_014601 INTRON OMIM: 605890 EHD2 EH domain-containing 2 chr1_229202018_r_154 154 DISC1 NM_018662 INTRON OMIM: 605210 DISC1 Disrupted in schizophrenia 1 Schizophrenia, 181500 (2) MOUSE: 8(Disc1) chr2_178380530_y_154 154 DKFZp451M2119 NM_182585 UTR chr3_125668165_y_154 154 TRAD NM_007064 INTRON OMIM: 603500 TRADD TNRF1-associated death domain protein MOUSE: 8(Tradd) chr3_143005243_r_154 154 TFDP2 NM_006286 INTRON OMIM: 602160 TFDP2, DP2 Transcription factor Dp-2 (E2F dimerization partner 2) chr3_152144903_y_154 154 TRALPUSH NM_053002 INTRON chr3_89204966_y_154 154 EPHA3 NM_005233 INTRON OMIM: 179611 EPHA3, ETK1, HEK Ephrin receptor EphA3 (human embryo kinase 1) chr3_89204966_y_154 154 EPHA3 NM_182644 INTRON OMIM: 179611 EPHA3, ETK1, HEK Ephrin receptor EphA3 (human embryo kinase 1) chr5_140349268_y_154 154 PCDHA1 NM_018900 INTRON OMIM: 606307 PCDHA1 Protocadherin-alpha 1 chr5_140349268_y_154 154 PCDHA1 NM_031411 INTRON OMIM: 606307 PCDHA1 Protocadherin-alpha 1 chr5_140349268_y_154 154 PCDHA2 NM_018905 INTRON OMIM: 606308 PCDHA2 Protocadherin-alpha 2 chr5_140349268_y_154 154 PCDHA3 NM_018906 INTRON OMIM: 606309 PCDHA3 Protocadherin-alpha 3 chr5_140349268_y_154 154 PCDHA4 NM_018907 INTRON OMIM: 606310 PCDHA4 Protocadherin-alpha 4 chr5_140349268_y_154 154 PCDHA5 NM_018908 INTRON OMIM: 606311 PCDHA5 Protocadherin-alpha 5 chr5_140349268_y_154 154 PCDHA6 NM_018909 INTRON OMIM: 606312 PCDHA6 Protocadherin-alpha 6 chr5_140349268_y_154 154 PCDHA6 NM_031849 INTRON OMIM: 606312 PCDHA6 Protocadherin-alpha 6 chr5_140349268_y_154 154 PCDHA7 NM_018910 INTRON OMIM: 606313 PCDHA7 Protocadherin-alpha 7 chr5_140349268_y_154 154 PCDHA8 NM_018911 INTRON OMIM: 606314 PCDHA8 Protocadherin-alpha 8 chr5_140349268_y_154 154 PCDHA9 NM_031857 INTRON OMIM: 606315 PCDHA9 Protocadherin-alpha 9 chr5_140349268_y_154 154 PCDHA10 NM_018901 INTRON OMIM: 606316 PCDHA10 Protocadherin-alpha 10 chr5_140349268_y_154 154 PCDHA10 NM_031860 INTRON OMIM: 606316 PCDHA10 Protocadherin-alpha 10 chr5_140349268_y_154 154 PCDHA11 NM_018902 INTRON OMIM: 606317 PCDHA11 Protocadherin-alpha 11 chr5_140349268_y_154 154 PCDHA12 NM_018903 INTRON OMIM: 606318 PCDHA12 Protocadherin-alpha 12 chr5_140349268_y_154 154 PCDHA13 NM_018904 INTRON OMIM: 606319 PCDHA13 Protocadherin-alpha 13 chr5_140349268_y_154 154 PCDHAC1 NM_018898 INTRON OMIM: 606320 PCDHAC1 Protocadherin-alpha, subfamily C, member 1 chr8_27798361_r_154 154 MGC45780 NM_173833 INTRON chrX_105189100_y_154 154 FLJ20130 NM_017681 INTRON chrX_7924805_r_154 154 KAL1 NM_000216 INTRON OMIM: 308700 KAL1, KMS, ADMLX Kallmann syndrome-1 sequence (anosmin-1) with ichthyosis in probable microdeletion syndrome Kallmann syndrome (3) chr14_54072538_y_155 155 KTN1 NM_004986 INTRON OMIM: 600381 KTN1, CG1 Kinectin chr14_90829251_y_155 155 SLC24A4 NM_153648 INTRON chr14_90829251_y_155 155 SLC24A4 NM_153646 INTRON chr14_90829251_y_155 155 SLC24A4 NM_153647 INTRON chr16_74283713_y_155 155 GLG1 NM_012201 INTRON OMIM: 600753 GLG1 Golgi apparatus protein 1 MOUSE: 8(Glg1) chr17_28702601_r_155 155 SLC6A4 NM_001045 UTR OMIM: 182138 SLC6A4, HTT Solute carrier family 6 (neurotransmitter transporter, serotonin),member 4 Anxiety-related personality traits (3) MOUSE: 11(Htt) chr3_166028038_r_155 155 SI NM_001041 INTRON OMIM: 181590 SIL SCL interrupting locus within about 250kb of SCL chr3_166835891_y_155 155 BCHE NM_000055 INTRON OMIM: 177400 BCHE, CHE1 Butyrylcholinesterase distal to CP, TF Apnea, postanesthetic (3) chr3_193285526_r_155 155 FGF12 NM_021032 INTRON OMIM: 601513 FGF12, FHF1 Fibroblast growth factor-12 MOUSE: 16(Fhf1) chr3_193285526_r_155 155 FGF12 NM_004113 INTRON OMIM: 601513 FGF12, FHF1 Fibroblast growth factor-12 MOUSE: 16(Fhf1) chr4_154276276_r_155 155 TIGD4 NM_145720 UTR chr6_162566190_r_155 155 PARK2 NM_004562 INTRON OMIM: 602544 PRKN, PARK2, PDJ Parkin Parkinson disease, juvenile, type 2, 600116 (3); Adenocarcinoma oflung, somatic, MOUSE: 17(Park2) chr6_162566190_r_155 155 PARK2 NM_013987 INTRON OMIM: 602544 PRKN, PARK2, PDJ Parkin Parkinson disease, juvenile, type 2, 600116 (3); Adenocarcinoma oflung, somatic, MOUSE: 17(Park2) chr6_162566190_r_155 155 PARK2 NM_013988 INTRON OMIM: 602544 PRKN, PARK2, PDJ Parkin Parkinson disease, juvenile, type 2, 600116 (3); Adenocarcinoma oflung, somatic, MOUSE: 17(Park2) chr6_20780373_y_155 155 CDKAL1 NM_017774 INTRON chr7_110739707_r_155 155 IMMP2L NM_032549 UTR OMIM: 605977 IMP2, IMMP2L Inner mitochondrial membrane peptidase, subunit 2, yeast, homolog of chrX_10970322_r_155 155 ARHGAP6 NM_001174 UTR OMIM: 300118 ARHGAP6 Rho GTPase-activating protein-6 chrX_10970322_r_155 155 ARHGAP6 NM_013427 INTRON OMIM: 300118 ARHGAP6 Rho GTPase-activating protein-6 chrX_10970322_r_155 155 ARHGAP6 NM_006125 INTRON OMIM: 300118 ARHGAP6 Rho GTPase-activating protein-6 chrX_66754822_y_155 155 STARD8 NM_014725 UTR chr10_119477213_y_156 156 C10orf5 NM_178816 UTR chr11_6499973_y_156 156 FLJ35709 NM_173589 INTRON chr12_26560411_r_156 156 ITPR2 NM_002223 INTRON OMIM: 600144 ITPR2 Inositol 1,4,5-triphosphate receptor, type 2 chr19_40330736_r_156 156 FXYD7 NM_022006 INTRON OMIM: 606684 FXYD7 FXYD domain-containing ion transport regulator 7 chr1_180133188_r_156 156 C1orf14 NM_030933 INTRON chr1_213798991_r_156 156 ESRRG NM_001438 INTRON OMIM: 602969 ESRRG Estrogen-related receptor, gamma chr1_75100064_y_156 156 MGC34032 NM_152697 INTRON chr1_97743456_r_156 156 DPYD NM_000110 INTRON OMIM: 274270 DPYD, DPD Dihydropyrimidine dehydrogenase Thymine-uraciluria (3); {Fluorouracil toxicity, sensitivity to} (3) chr20_17367513_r_156 156 PCSK2 NM_002594 INTRON OMIM: 162151 PCSK2, NEC2, PC2 Proprotein convertase subtilisin/kexin type 2 MOUSE: 2(Nec2) chr21_33101952_y_156 156 C21orf62 NM_019596 UTR chr3_100988315_r_156 156 MGC4308 NM_032359 INTRON chr5_139346928_r_156 156 NRG2 NM_004883 INTRON OMIM: 603818 NRG2 Neruregulin 2 chr5_139346928_r_156 156 NRG2 NM_013981 INTRON OMIM: 603818 NRG2 Neruregulin 2 chr5_139346928_r_156 156 NRG2 NM_013982 INTRON OMIM: 603818 NRG2 Neruregulin 2 chr5_139346928_r_156 156 NRG2 NM_013983 INTRON OMIM: 603818 NRG2 Neruregulin 2 chr5_139346928_r_156 156 NRG2 NM_013984 INTRON OMIM: 603818 NRG2 Neruregulin 2 chr5_139346928_r_156 156 NRG2 NM_013985 INTRON OMIM: 603818 NRG2 Neruregulin 2 chr11_83209764_r_157 157 DLG2 NM_001364 INTRON OMIM: 603583 DLG2 Discs large, Drosophila, homolog of, 2(channel-associated protein of synapses, 1 chr12_111527991_r_157 157 RPH3A NM_014954 UTR OMIM: 604881 RPH3AL, NOC2 Rabphilin 3A-like chr12_2050401_y_157 157 CACNA1C NM_000719 INTRON OMIM: 114205 CACNA1C, CACNL1A1, C Calcium channel, voltage-dependent, L type, alpha 1C subunit chr17_32271909_y_157 157 ACCN1 NM_001094 INTRON OMIM: 601784 ACCN1, BNC1, MDEG Amiloride-sensitive cation channel 1, neuronal (degenerin) chr22_25069228_r_157 157 SEZ6L NM_021115 INTRON OMIM: 607021 SEZ6L Seizure-related 6-like chr3_193197004_y_157 157 FGF12 NM_021032 INTRON OMIM: 601513 FGF12, FHF1 Fibroblast growth factor-12 MOUSE: 16(Fhf1) chr3_193197004_y_157 157 FGF12 NM_004113 INTRON OMIM: 601513 FGF12, FHF1 Fibroblast growth factor-12 MOUSE: 16(Fhf1) chr4_89856764_r_157 157 CEB1 NM_016323 INTRON OMIM: 600695 TCEB1L, OCP2 Transcription elongation factor B (SIII), polypeptide 1-like chr8_126289007_r_157 157 FLJ32440 NM_173685 INTRON chr8_51664231_y_157 157 SNTG1 NM_018967 INTRON chrX_84637160_y_157 157 DACH2 NM_053281 INTRON chr13_98648841_y_158 158 PCCA NM_000282 INTRON OMIM: 232000 PCCA Propionyl Coenzyme A carboxylase, alpha polypeptide Propionicacidemia, 606054 (3) MOUSE: 14(Pcca) chr14_28379248_r_158 158 PRKCM NM_002742 INTRON OMIM: 605435 PRKCM Protein kinase C, mu also assigned to chr.21 chr15_61235883_y_158 158 LOC51762 NM_016530 INTRON chr19_59671889_y_158 158 CDC42EP5 NM_145057 UTR chr1_165455377_y_158 158 TBX19 NM_005149 INTRON chr4_7361211_y_158 158 SORCS2 NM_020777 INTRON OMIM: 606284 SORCS2, KIAA1329 SORCS receptor 2 chr9_72911861_r_158 158 TRPM6 NM_017662 INTRON OMIM: 607009 TRPM6, CHAK2 Transient receptor potential cation channel, subfamily M, member 6 Hypomagnesemia with secondary hypocalcemia, 602014 (3) chr9_81434814_y_158 158 MGC20553 NM_174938 INTRON chr11_107981446_r_159 159 SLAC2-B NM_015065 INTRON chr11_122271589_r_159 159 CRTAM NM_019604 INTRON chr11_99498881_y_159 159 CNTN5 NM_014361 INTRON OMIM: 607219 CNTN5, NB2 Contactin 5 chr11_99498881_y_159 159 CNTN5 NM_175566 INTRON OMIM: 607219 CNTN5, NB2 Contactin 5 chr12_127809221_y_159 159 FLJ31978 NM_144669 INTRON chr14_86656341_y_159 159 KCNK10 NM_138318 INTRON OMIM: 605873 KCNK10, TREK2 Potassium channel, subfamily K, member 10 chr14_86656341_y_159 159 KCNK10 NM_138317 INTRON OMIM: 605873 KCNK10, TREK2 Potassium channel, subfamily K, member 10 chr14_86656341_y_159 159 KCNK10 NM_021161 INTRON OMIM: 605873 KCNK10, TREK2 Potassium channel, subfamily K, member 10 chr15_76223813_r_159 159 BG1 NM_015162 INTRON OMIM: 142200 HBG1 Hemoglobin, gamma A HPFH, nondeletion type A (3) chr16_46541638_r_159 159 LOC91807 NM_182493 INTRON chr16_6264943_r_159 159 A2BP1 NM_018723 UTR chr17_40631369_r_159 159 LGP2 NM_024119 INTRON chr18_65710579_r_159 159 DNAM-1 NM_006566 INTRON chr1_200916975_r_159 159 LAX NM_017773 UTR chr1_244551096_y_159 159 CIAS1 NM_004895 INTRON OMIM: 606416 CIAS1, C1orf7, FCU, Cryopyrin Cold-induced autoinflammatory syndrome, familial, 120100 (3);Muckle-Wells syndro chr2_223347468_r_159 159 PAX3 NM_181457 INTRON OMIM: 606597 PAX3, WS1, HUP2, CDH Paired box homeotic gene-3 Waardenburg syndrome, type I, 193500 (3); Waardenburg syndrome, typeIII, 148820 MOUSE: 1(Sp) chr2_223347468_r_159 159 PAX3 NM_181458 INTRON OMIM: 606597 PAX3, WS1, HUP2, CDH Paired box homeotic gene-3 Waardenburg syndrome, type I, 193500 (3); Waardenburg syndrome, typeIII, 148820 MOUSE: 1(Sp) chr2_223347468_r_159 159 PAX3 NM_181459 INTRON OMIM: 606597 PAX3, WS1, HUP2, CDH Paired box homeotic gene-3 Waardenburg syndrome, type I, 193500 (3); Waardenburg syndrome, typeIII, 148820 MOUSE: 1(Sp) chr2_223347468_r_159 159 PAX3 NM_181460 INTRON OMIM: 606597 PAX3, WS1, HUP2, CDH Paired box homeotic gene-3 Waardenburg syndrome, type I, 193500 (3); Waardenburg syndrome, typeIII, 148820 MOUSE: 1(Sp) chr2_223347468_r_159 159 PAX3 NM_181461 INTRON OMIM: 606597 PAX3, WS1, HUP2, CDH Paired box homeotic gene-3 Waardenburg syndrome, type I, 193500 (3); Waardenburg syndrome, typeIII, 148820 MOUSE: 1(Sp) chr2_231564714_r_159 159 SP100 NM_003113 INTRON OMIM: 604585 SP100 Nuclear antigen SP100 chr2_26145985_r_159 159 KIF3C NM_002254 INTRON OMIM: 602845 KIF3C Kinesin family member 3C MOUSE: 12(Kif3c) chr2_9699738_r_159 159 ADAM17 NM_003183 INTRON OMIM: 603639 ADAM17, TACE A disintegrin and metalloproteinase domain 17 MOUSE: 12(Tace) chr2_9699738_r_159 159 ADAM17 NM_021832 INTRON OMIM: 603639 ADAM17, TACE A disintegrin and metalloproteinase domain 17 MOUSE: 12(Tace) chr3_120647896_r_159 159 PLA1A NM_015900 INTRON OMIM: 607460 PLA1A, PSPLA1 Phosphatidylserine-specific phospholipase A1-alpha MOUSE: 16(Pla1a) chr3_189400119_y_159 159 LPP NM_005578 UTR OMIM: 171800 ALPP Alkaline phosphatase, placental (Regan isozyme) MOUSE: 4(Akp2) chr4_81395403_r_159 159 CMG2 NM_058172 UTR chr5_64108446_y_159 159 SDCCAG10 NM_005869 INTRON chr6_10570316_r_159 159 PAK1IP1 NM_017906 UTR chr7_115949373_r_159 159 MET NM_000245 INTRON OMIM: 601916 ARMET, ARP Arginine-rich protein, mutated in early stage tumors Pancreatic cancer, 260350 (3) chr7_139091682_r_159 159 TBXAS1 NM_001061 INTRON OMIM: 274180 TBXAS1 Thromboxane A synthase 1, platelet Thromboxane synthase deficiency (2) MOUSE: 6(Tbxas1) chr7_139091682_r_159 159 TBXAS1 NM_030984 INTRON OMIM: 274180 TBXAS1 Thromboxane A synthase 1, platelet Thromboxane synthase deficiency (2) MOUSE: 6(Tbxas1) chr12_26610041_r_160 160 ITPR2 NM_002223 INTRON OMIM: 600144 ITPR2 Inositol 1,4,5-triphosphate receptor, type 2 chr13_26383793_y_160 160 FLT3 NM_004119 INTRON OMIM: 136351 FLT3 fms-related tyrosine kinase-3 Leukemia, acute myeloid, reduced survival in (3); Leukemia,acute myeloid (3) MOUSE: 5(Flt3) chr15_50240475_r_160 160 MYO5C NM_018728 INTRON chr1_43696286_y_160 160 SIAT6 NM_006279 INTRON OMIM: 606494 SIAT6, ST3GALII Sialyltransferase 6 chr1_43696286_y_160 160 SIAT6 NM_174963 INTRON OMIM: 606494 SIAT6, ST3GALII Sialyltransferase 6 chr1_43696286_y_160 160 SIAT6 NM_174964 INTRON OMIM: 606494 SIAT6, ST3GALII Sialyltransferase 6 chr1_43696286_y_160 160 SIAT6 NM_174965 INTRON OMIM: 606494 SIAT6, ST3GALII Sialyltransferase 6 chr1_43696286_y_160 160 SIAT6 NM_174966 INTRON OMIM: 606494 SIAT6, ST3GALII Sialyltransferase 6 chr1_43696286_y_160 160 SIAT6 NM_174967 INTRON OMIM: 606494 SIAT6, ST3GALII Sialyltransferase 6 chr1_43696286_y_160 160 SIAT6 NM_174968 INTRON OMIM: 606494 SIAT6, ST3GALII Sialyltransferase 6 chr1_43696286_y_160 160 SIAT6 NM_174969 INTRON OMIM: 606494 SIAT6, ST3GALII Sialyltransferase 6 chr1_43696286_y_160 160 SIAT6 NM_174970 INTRON OMIM: 606494 SIAT6, ST3GALII Sialyltransferase 6 chr1_43696286_y_160 160 SIAT6 NM_174971 INTRON OMIM: 606494 SIAT6, ST3GALII Sialyltransferase 6 chr1_43696286_y_160 160 SIAT6 NM_174972 INTRON OMIM: 606494 SIAT6, ST3GALII Sialyltransferase 6 chr2_62220691_y_160 160 MURR1 NM_152516 INTRON OMIM: 607238 MURR1 Copper metabolism gene chr4_186293575_y_160 160 FLJ33167 NM_152683 INTRON chr4_41077439_r_160 160 APBB2 NM_173075 UTR OMIM: 602710 APBB2, FE65L1 Amyloid beta A4 precursor protein-binding, family B, member 2(Fe65-like 1) chr4_46894773_r_160 160 GABRA4 NM_000809 INTRON OMIM: 137141 GABRA4 Gamma-aminobutyric acid (GABA) A receptor, alpha-4 cluster with GABRA2, B1, G1 MOUSE: 7(Gabra4) chr4_46894773_r_160 160 COX7B2 NM_130902 UTR chr6_129350144_y_160 160 LAMA2 NM_000426 INTRON OMIM: 156225 LAMA2, LAMM Laminin, alpha-2 (merosin) Muscular dystrophy, congenital merosin-deficient, 607855 (3);Muscular dystrophy, MOUSE: 10(dy, Lamm) chr7_143825850_r_160 160 TPK1 NM_022445 INTRON OMIM: 606370 TPK1 Thiamine pyrophosphokinase chr7_86789460_r_160 160 ABCB1 NM_000927 INTRON OMIM: 605454 ABCB10, MTABC2 ATP-binding cassette, subfamily B, member 10 pseudogene on 15q13-q14 chrX_47368140_r_160 160 SLC38A5 NM_033518 INTRON chr13_100511917_r_161 161 FGF14 NM_175929 INTRON OMIM: 601515 FGF14, FHF4 Fibroblast growth factor-14 Cerebellar ataxia, autosomal dominant, FGF14-related (3) MOUSE: 14(Fhf4) chr14_75726048_y_161 161 NGB NM_021257 INTRON OMIM: 605080 CNGB3, ACHM3 Cyclic nucleotide-gated channel, beta-3 Achromatopsia-3, 262300 (3) chr15_71896693_y_161 161 MGC34741 NM_153356 INTRON chr19_53415978_r_161 161 TUCAN NM_014959 INTRON chr1_32234774_y_161 161 LCK NM_005356 UTR OMIM: 153390 LCK Lymphocyte-specific protein tyrosine kinase LCK/TCRB fusion in leukemia SCID due to LCK deficiency (1) MOUSE: 4(Lck) chr1_42100916_r_161 161 KIAA1041 NM_014947 INTRON chr22_28878993_y_161 161 MGC26710 NM_152510 INTRON chr3_112820004_r_161 161 FLJ31579 NM_153268 INTRON chr3_160751856_r_161 161 SCHIP1 NM_014575 INTRON chr6_20865014_y_161 161 CDKAL1 NM_017774 INTRON chr7_131662498_y_161 161 DKFZp434G0625 NM_181775 UTR chr9_133000358_y_161 161 COL5A1 NM_000093 INTRON OMIM: 120215 COL5A1 Collagen V, alpha-1 polypeptide Ehlers-Danlos syndrome, type II, 130010 (3); Ehlers-Danlos syndrome,type I, 1300 MOUSE: 2(Col5a1) chr9_85678715_y_161 161 DAPK1 NM_004938 INTRON OMIM: 600831 DAPK1 Death-associated protein kinase-1 chrX_1144752_r_161 161 IL3RA NM_002183 INTRON OMIM: 308385 IL3RA Interleukin-3 receptor, alpha subunit same 190kb segment as CSF2RA MOUSE: 14(Il3ra) chrX_146560693_r_161 161 FMR2 NM_002025 INTRON OMIM: 309548 FMR2, FRAXE, MRX2 Fragile site, X-linked, E Mental retardation, X-linked, FRAXE type (3) chrY_1144752_r_161 161 IL3RA NM_002183 INTRON OMIM: 308385 IL3RA Interleukin-3 receptor, alpha subunit same 190kb segment as CSF2RA MOUSE: 14(Il3ra) chr11_16359647_r_162 162 SOX6 NM_033326 UTR OMIM: 607257 SOX6 SRY-box 6 MOUSE: 7(Sox6) chr17_17690018_r_162 162 PEMT NM_148172 INTRON chr18_40543311_y_162 162 SETBP1 NM_015559 INTRON chr18_53529371_y_162 162 ATP8B1 NM_005603 INTRON OMIM: 602397 ATP8B1, FIC1, BRIC, ATPase, class I, type 8B, member 1 Cholestasis, progressive familial intrahepatic 1, 211600 (3);Cholestasis, benign chr19_6275776_r_162 162 LOC125981 NM_133492 INTRON chr1_234720236_y_162 162 RYR2 NM_001035 INTRON OMIM: 180902 RYR2, VTSIP Ryanodine receptor-2 (cardiac) Ventricular tachycardia, stress-induced polymorphic, 604772 (3);Arrhythmogenic r MOUSE: 13(Ryr2) chr1_65354530_y_162 162 LEPR NM_002303 UTR OMIM: 601007 LEPR, OBR Leptin receptor Obesity, morbid, with hypogonadism (3) MOUSE: 4(Lepr) chr21_25969679_r_162 162 JAM2 NM_021219 INTRON OMIM: 606870 JAM2, VEJAM Junctional adhesion molecule 2 chr4_169855422_r_162 162 FLJ20035 NM_017631 INTRON chr5_151257448_y_162 162 GLRA1 NM_000171 INTRON OMIM: 138491 GLRA1, STHE Glycine receptor, alpha-1 polypeptide Startle disease/hyperekplexia, autosomal dominant, 149400 (3);Startle disease, a MOUSE: 11(spd) chr6_44378173_y_162 162 FLJ25442 NM_145026 INTRON chr7_151070362_y_162 162 GALNT15 NM_145292 INTRON chr8_141165008_r_162 162 MGC4737 NM_031466 UTR chrX_105204875_r_162 162 FLJ20130 NM_017681 UTR chr10_111343122_r_163 163 XPNPEP1 NM_020383 UTR OMIM: 602443 XPNPEP1, SAMP, XPNPE X-prolyl aminopeptidase P1 chr12_1397992_y_163 163 ELKS NM_015064 UTR chr12_54520369_r_163 163 MMP19 NM_002429 INTRON OMIM: 601807 MMP19, MMP18 Matrix metalloproteinase-19 chr12_54520369_r_163 163 MMP19 NM_022791 INTRON OMIM: 601807 MMP19, MMP18 Matrix metalloproteinase-19 chr13_26784414_y_163 163 FLT1 NM_002019 INTRON OMIM: 165070 FLT1 fms-related tyrosine kinase-1 (vascular endothelial growthfactor/vascular permea 150kb from FLT3 chr1_21432780_r_163 163 RAP1GA1 NM_002885 UTR OMIM: 600278 RAP1GA1 RAP1, GTPase activating protein 1 chr1_238072447_r_163 163 RGS7 NM_002924 INTRON chr1_99611486_r_163 163 PALMD NM_017734 INTRON chr2_28512389_r_163 163 BRE NM_004899 INTRON OMIM: 275355 TGFBRE, TGFR Transforming growth factor, beta-1 response element distal 18q chr4_102485915_r_163 163 PPP3CA NM_000944 INTRON OMIM: 114105 PPP3CA, PPP2B, CALNA Protein phosphatase-3 (formerly 2B), catalytic subunit, alpha isoform(calcineuri chr5_139827806_y_163 163 FLJ20288 NM_024668 UTR chr5_52146195_r_163 163 ITGA1 NM_181501 INTRON OMIM: 192968 ITGA1, VLA1 Integrin, alpha-1 close to Ctla-3 in mouse MOUSE: 13(Vla1) chr6_22401771_r_163 163 PRL NM_000948 INTRON OMIM: 601584 PTP4A2, PTP4A, PRL2, Protein tyrosine phosphatase, type 4A, 2 chr8_102584838_y_163 163 FLJ13782 NM_024915 INTRON chr9_105431127_y_163 163 RAD23B NM_002874 INTRON OMIM: 600062 RAD23B RAD23 (Saccharomyces cerevisiae) homolog of, B previously 3p25.1 MOUSE: 4(Rad23b) chr9_3261421_y_163 163 RFX3 NM_134428 INTRON chr9_3261421_y_163 163 RFX3 NM_002919 INTRON chrX_148607049_r_163 163 CD99L2 NM_031462 INTRON chr10_69607169_r_164 164 SLC25A16 NM_152707 INTRON OMIM: 139080 SLC25A16, D10S105E, Solute carrier family 25 (mitochondrial carrier), member 16(Graves disease autoa chr11_57052427_r_164 164 POV1 NM_003627 INTRON OMIM: 603733 POV1 Prostate cancer overexpressed gene 1 chr11_9462968_y_164 164 ZNF143 NM_003442 INTRON OMIM: 603433 ZNF143, SBF Zinc finger protein-143 chr1_148293817_y_164 164 MGC29891 NM_144618 INTRON chr1_204171332_y_164 164 TOSO NM_005449 INTRON chr1_54655355_y_164 164 FLJ40201 NM_152607 INTRON chr20_45755695_r_164 164 DKFZp547G0215 NM_173643 UTR chr21_46420525_y_164 164 FTCD NM_006657 INTRON OMIM: 606806 FTCD Formiminotransferase cyclodeminase Glutamate formiminotransferase deficiency, 229100 (3) MOUSE: 10(Ftcd) chr4_91200780_r_164 164 SNCA NM_000345 INTRON OMIM: 163890 SNCA, NACP, PARK1 Synuclein, alpha (non A4 component of amyloid precursor) Parkinson disease, familial, 168601 (3) chr4_91200780_r_164 164 SNCA NM_007308 INTRON OMIM: 163890 SNCA, NACP, PARK1 Synuclein, alpha (non A4 component of amyloid precursor) Parkinson disease, familial, 168601 (3) chr5_155851957_y_164 164 SGCD NM_172244 INTRON OMIM: 601411 SGCD, SGD, LGMD2F, C Sarcoglycan, delta (35kD dystrophin-associated glycoprotein) mutant in Syrian hamster cardiomyopathy Muscular dystrophy, limb-girdle, type 2F, 601287 (3); Cardiomyopathy,dilated, 1L chr5_155851957_y_164 164 SGCD NM_000337 INTRON OMIM: 601411 SGCD, SGD, LGMD2F, C Sarcoglycan, delta (35kD dystrophin-associated glycoprotein) mutant in Syrian hamster cardiomyopathy Muscular dystrophy, limb-girdle, type 2F, 601287 (3); Cardiomyopathy,dilated, 1L chr6_135646320_y_164 164 FLJ20069 NM_017651 INTRON chr7_110481744_r_164 164 IMMP2L NM_032549 INTRON OMIM: 605977 IMP2, IMMP2L Inner mitochondrial membrane peptidase, subunit 2, yeast, homolog of chr7_131663883_y_164 164 DKFZp434G0625 NM_181775 UTR chr8_32182233_r_164 164 NRG1 NM_013962 INTRON OMIM: 142445 NRG1, HGL, HRGA, ARI Neuregulin 1 (heregulin, alpha, 45kD; ERBB2 p185-activator) {?Schizophrenia, susceptibility to}, 603013 (1) MOUSE: 7(Nrg1) chrX_112639658_y_164 164 HTR2C NM_000868 UTR OMIM: 312861 HTR2C 5-hydroxytryptamine (serotonin) receptor-2C formerly HTR1C MOUSE: X(Htr2c) chr15_86925381_y_165 165 ISG20 NM_002201 INTRON OMIM: 604533 ISG20, HEM45 Interferon-stimulated gene, 20kD chr1_56956685_r_165 165 DAB1 NM_021080 INTRON OMIM: 603448 DAB1 Disabled, Drosophila, homolog 1 MOUSE: 4(Dab1) chr22_24720026_y_165 165 MYO18B NM_032608 INTRON OMIM: 607295 MYO18B Myosin XVIIIB chr2_228260958_r_165 165 COL4A3 NM_000091 INTRON OMIM: 120070 COL4A3 Collagen IV, alpha-3 polypeptide (Goodpasture antigen) noncollagenous domain = Goodpasture antigen Alport syndrome, autosomal recessive, 203780 (3) chr2_228260958_r_165 165 COL4A3 NM_031362 INTRON OMIM: 120070 COL4A3 Collagen IV, alpha-3 polypeptide (Goodpasture antigen) noncollagenous domain = Goodpasture antigen Alport syndrome, autosomal recessive, 203780 (3) chr2_228260958_r_165 165 COL4A3 NM_031363 INTRON OMIM: 120070 COL4A3 Collagen IV, alpha-3 polypeptide (Goodpasture antigen) noncollagenous domain = Goodpasture antigen Alport syndrome, autosomal recessive, 203780 (3) chr2_228260958_r_165 165 COL4A3 NM_031364 INTRON OMIM: 120070 COL4A3 Collagen IV, alpha-3 polypeptide (Goodpasture antigen) noncollagenous domain = Goodpasture antigen Alport syndrome, autosomal recessive, 203780 (3) chr2_228260958_r_165 165 COL4A3 NM_031365 INTRON OMIM: 120070 COL4A3 Collagen IV, alpha-3 polypeptide (Goodpasture antigen) noncollagenous domain = Goodpasture antigen Alport syndrome, autosomal recessive, 203780 (3) chr2_228260958_r_165 165 COL4A3 NM_031366 INTRON OMIM: 120070 COL4A3 Collagen IV, alpha-3 polypeptide (Goodpasture antigen) noncollagenous domain = Goodpasture antigen Alport syndrome, autosomal recessive, 203780 (3) chr2_71015149_y_165 165 CLECSF13 NM_173535 INTRON chr3_121279132_y_165 165 GABABL NM_153002 INTRON chr3_123492249_r_165 165 KPNA1 NM_002264 INTRON OMIM: 600686 KPNA1, RCH2, SRP1 Karyopherin, alpha-1 chr5_81373174_y_165 165 APG10L NM_031482 INTRON chr6_38888853_y_165 165 DNAH8 NM_001371 INTRON chr6_47710639_y_165 165 GPR115 NM_153838 INTRON chr7_5539041_r_165 165 TRIAD3 NM_019011 UTR chr8_140779315_r_165 165 MGC4737 NM_031466 INTRON chr10_93501093_r_166 166 CPEB3 NM_014912 INTRON chr19_53300918_y_166 166 PLA2G4C NM_003706 INTRON OMIM: 603602 PLA2G4C Phospholipase A2, group IVC chr1_164662827_y_166 166 CD3Z NM_000734 INTRON OMIM: 186780 CD3Z, TCRZ CD3Z antigen, zeta polypeptide (TiT3 complex) CD3, zeta chain, deficiency (1) MOUSE: 1(T3z, Cd3z) chr1_234795526_y_166 166 RYR2 NM_001035 INTRON OMIM: 180902 RYR2, VTSIP Ryanodine receptor-2 (cardiac) Ventricular tachycardia, stress-induced polymorphic, 604772 (3);Arrhythmogenic r MOUSE: 13(Ryr2) chr2_142512634_y_166 166 LRP1B NM_018557 INTRON chr2_161485272_r_166 166 RBMS1 NM_002897 INTRON chr2_161485272_r_166 166 RBMS1 NM_016836 INTRON chr2_161485272_r_166 166 RBMS1 NM_016837 INTRON chr2_161485272_r_166 166 RBMS1 NM_016839 UTR chr2_240375746_r_166 166 HDAC4 NM_006037 INTRON OMIM: 605314 HDAC4, HDACA Histone deacetylase 4 chr6_42277028_r_166 166 TReP-132 NM_018415 INTRON chr6_42277028_r_166 166 TReP-132 NM_033501 INTRON chr6_42277028_r_166 166 TReP-132 NM_033502 INTRON chr7_150871110_r_166 166 PRKAG2 NM_016203 INTRON OMIM: 602743 PRKAG2, WPWS Protein kinase, AMP-activated, noncatalytic, gamma-2 Wolff-Parkinson-White syndrome, 194200 (3); Cardiomyopathy,hypertrophic, with WP chr7_37662893_r_166 166 TXNDC3 NM_016616 INTRON chr7_88412632_y_166 166 FLJ32110 NM_181646 INTRON chr8_77700786_y_166 166 ZFH4 NM_024721 INTRON OMIM: 606940 ZFH4 Zinc finger homeodomain 4 ?Ptosis, congenital, 178300 (2) chr10_67370373_r_167 167 VR22 NM_013266 INTRON chr13_110985380_r_167 167 LOC122258 NM_145248 INTRON chr18_54050237_y_167 167 NEDD4L NM_015277 INTRON OMIM: 606384 NEDD4L, KIAA0439, RS Ubiquitin protein ligase NEDD4-like chr1_199181255_r_167 167 LMOD1 NM_012134 INTRON chr1_199181255_r_167 167 ELF3 NM_004433 UTR OMIM: 602191 ELF3, ESX E74-like factor 3 (ETS domain transcription factor, serine box,epithelial-specif chr1_28860845_y_167 167 OPRD1 NM_000911 INTRON OMIM: 165195 OPRD1 Opioid receptor, delta-1 MOUSE: 4(Nbor, Oprd1) chr1_41601369_y_167 167 HIVEP3 NM_024503 UTR OMIM: 606649 HIVEP3, KRC Human immunodeficiency virus type 1 enhancer-binding protein 3 chr20_32599189_r_167 167 C20orf114 NM_033197 INTRON chr2_162992184_y_167 167 SLC4A10 NM_022058 INTRON OMIM: 605556 SLC4A10 Solute carrier family 4 (sodium bicarbonate cotransporter-like),member 10 chr2_175694666_y_167 167 WASPIP NM_003387 UTR chr4_53788986_r_167 167 STXBP1L1 NM_152540 INTRON chr9_125859153_y_167 167 FLJ32780 NM_144965 INTRON chrY_5174804_r_167 167 PCDH11Y NM_032973 INTRON OMIM: 400022 PCDH11Y, PCDH22, PCD Protocadherin 22 chr11_83655542_r_168 168 DLG2 NM_001364 INTRON OMIM: 603583 DLG2 Discs large, Drosophila, homolog of, 2(channel-associated protein of synapses, 1 chr11_88362759_r_168 168 GRM5 NM_000842 INTRON chr12_51522965_r_168 168 K5B NM_173352 INTRON chr15_86225126_r_168 168 NTRK3 NM_002530 INTRON OMIM: 191316 NTRK3, TRKC Neurotrophic tyrosine kinase, receptor, type 3 chr18_11997553_y_168 168 IMPA2 NM_014214 INTRON OMIM: 605922 IMPA2 Myo-inositol monophosphatase 2 chr2_113973683_y_168 168 IL1RN NM_000577 INTRON OMIM: 147679 IL1RN Interleukin-1 receptor antagonist chr2_113973683_y_168 168 IL1RN NM_173841 INTRON OMIM: 147679 IL1RN Interleukin-1 receptor antagonist chr2_113973683_y_168 168 IL1RN NM_173843 UTR OMIM: 147679 IL1RN Interleukin-1 receptor antagonist chr2_163373391_y_168 168 MDA5 NM_022168 INTRON chr2_183452975_y_168 168 PDE1A NM_005019 INTRON OMIM: 171890 PDE1A Phosphodiesterase-1A chr3_110080102_r_168 168 MORC NM_014429 INTRON OMIM: 603205 MORC Microrchidia, mouse, homolog of MOUSE: 16(Morc) chr3_189663364_y_168 168 LPP NM_005578 INTRON OMIM: 171800 ALPP Alkaline phosphatase, placental (Regan isozyme) MOUSE: 4(Akp2) chr3_45128185_y_168 168 CDCP1 NM_022842 INTRON chr3_45128185_y_168 168 CDCP1 NM_178181 INTRON chr3_85077603_y_168 168 LOC253559 NM_153184 INTRON chr4_53414579_r_168 168 FLJ12552 NM_022832 INTRON chr5_56561535_y_168 168 DKFZp761C169 NM_022913 INTRON chr6_10678041_y_168 168 GCNT2 NM_145649 INTRON OMIM: 600429 GCNT2 Glucosaminyl (N-acetyl) transferase 2, I-branching enzyme previously assigned to 9q21 [Blood group, Ii], 110800 (3); Adult i phenotype with congenitalcataract, 110800 chr6_10678041_y_168 168 GCNT2 NM_001491 INTRON OMIM: 600429 GCNT2 Glucosaminyl (N-acetyl) transferase 2, I-branching enzyme previously assigned to 9q21 [Blood group, Ii], 110800 (3); Adult i phenotype with congenitalcataract, 110800 chr6_10678041_y_168 168 PAK1IP1 NM_017906 UTR chr7_100693215_y_168 168 COL26A1 NM_133457 INTRON chr7_156985995_y_168 168 PTPRN2 NM_002847 INTRON chr7_156985995_y_168 168 PTPRN2 NM_130842 INTRON chr7_156985995_y_168 168 PTPRN2 NM_130843 INTRON chr8_69734848_y_168 168 VEST1 NM_052958 INTRON chr9_114913993_r_168 168 ASTN2 NM_014010 INTRON chr12_127711688_y_169 169 FLJ31978 NM_144669 INTRON chr12_46539865_y_169 169 VDR NM_000376 INTRON OMIM: 601769 VDR Vitamin D (1,25-dihydroxyvitamin D3) receptor Rickets, vitamin D-resistant, type IIA, 277440 (3); Rickets, vitaminD-resistant, chr2_219382257_y_169 169 MR-1 NM_015488 INTRON chr3_12771623_y_169 169 FLJ11036 NM_018306 UTR chr4_73881919_r_169 169 ADAMTS3 NM_014243 INTRON OMIM: 605011 ADAMTS3 A Disintegrin-like and metalloproteinase with thrombospondin type 1motif, 3 chr5_52892402_y_169 169 NDUFS4 NM_002495 INTRON OMIM: 602694 NDUFS4, AQDQ NADH dehydrogenase (ubiquinone) Fe-S protein 4, 18kD (NADH-coenzyme Qreductase) Complex I deficiency, 252010 (3); Leigh syndrome, 256000(3) chr6_124487847_r_169 169 TCBA1 NM_153355 INTRON chr7_88397308_y_169 169 FLJ32110 NM_181646 INTRON chr7_98067997_r_169 169 DKFZp761L1417 NM_152913 INTRON chrX_106636089_y_169 169 COL4A5 NM_000495 INTRON OMIM: 303630 COL4A5, ATS, ASLN Collagen IV, alpha-5 polypeptide diffuse leiomyomatosis with Alport syndrome = contiguous genesyndrome with COL4A Alport syndrome, 301050 (3) MOUSE: X(Col4a5) chrX_106636089_y_169 169 COL4A5 NM_033380 INTRON OMIM: 303630 COL4A5, ATS, ASLN Collagen IV, alpha-5 polypeptide diffuse leiomyomatosis with Alport syndrome = contiguous genesyndrome with COL4A Alport syndrome, 301050 (3) MOUSE: X(Col4a5) chrX_106636089_y_169 169 COL4A5 NM_033381 INTRON OMIM: 303630 COL4A5, ATS, ASLN Collagen IV, alpha-5 polypeptide diffuse leiomyomatosis with Alport syndrome = contiguous genesyndrome with COL4A Alport syndrome, 301050 (3) MOUSE: X(Col4a5) chr12_274656_r_170 170 RBBP2 NM_005056 INTRON OMIM: 605393 RBBP2H1A Retinoblastoma-binding protein 2, homolog 1A chr14_94673004_r_170 170 BDKRB2 NM_000623 UTR OMIM: 113503 BDKRB2 Bradykinin receptor B2 chr17_71597345_r_170 170 C17orf26 NM_139177 INTRON chr17_8840814_r_170 170 FLJ32734 NM_144681 INTRON chr19_15144770_y_170 170 NOTCH3 NM_000435 INTRON OMIM: 600276 NOTCH3, CADASIL, CAS Notch, Drosophila, homolog of, 3 Cerebral arteriopathy with subcortical infarcts andleukoencephalopathy, 125310 ( MOUSE: 17(Notch3) chr19_18874474_r_170 170 COPE NM_007263 INTRON OMIM: 602053 COPEB, BCD1, ZF9 Core promoter element binding protein chr1_41517210_r_170 170 HIVEP3 NM_024503 UTR OMIM: 606649 HIVEP3, KRC Human immunodeficiency virus type 1 enhancer-binding protein 3 chr2_11275052_y_170 170 FLJ33534 NM_182586 INTRON chr2_125713125_y_170 170 caspr5 NM_130773 INTRON chr2_125713125_y_170 170 caspr5 NM_138996 INTRON chr2_47663568_y_170 170 MSH2 NM_000251 INTRON OMIM: 120435 MSH2, COCA1, FCC1, H mutS, E. coli, homolog of, 2 Colorectal cancer, hereditary nonpolyposis, type 1, 114500 (3);Ovarian cancer (3 chr2_47681846_y_170 170 MSH2 NM_000251 INTRON OMIM: 120435 MSH2, COCA1, FCC1, H mutS, E. coli, homolog of, 2 Colorectal cancer, hereditary nonpolyposis, type 1, 114500 (3);Ovarian cancer (3 chr5_147110619_r_170 170 KIAA0555 NM_014790 UTR chr7_104252012_y_170 170 MLL5 NM_018682 INTRON chr7_142511713_y_170 170 CLCN1 NM_000083 INTRON OMIM: 118425 CLCN1 Chloride channel-1, skeletal muscle Myotonia congenita, recessive, 255700 (3); Myotonia congenita,dominant, 160800 ( MOUSE: 6(adr, Clc1) chr8_126332330_r_170 170 FLJ32440 NM_173685 INTRON chrX_72525784_y_170 170 SLC16A2 NM_006517 INTRON OMIM: 300095 SLC16A2, DXS128, XPC Solute carrier family 16 (monocarboxylic acid transporters),member 2 chr10_100556457_r_171 171 HPSE2 NM_021828 INTRON chr10_132529571_r_171 171 LOC256536 NM_174937 INTRON chr10_18618535_y_171 171 CACNB2 NM_000724 INTRON OMIM: 600003 CACNB2 Calcium channel, voltage-dependent, beta 2 subunit chr10_55296451_r_171 171 PCDH15 NM_033056 INTRON OMIM: 605514 PCDH15 Protocadherin 15 Usher syndrome, type 1F, 602083 (3) MOUSE: 10(av) chr14_77476497_y_171 171 NRXN3 NM_004796 INTRON OMIM: 600567 NRXN3 Neurexin 3 chr16_31349746_y_171 171 ITGAM NM_000632 INTRON OMIM: 120980 ITGAM, CR3A, CD11B, Integrin, alpha-M (complement component receptor-3, alpha; antigenCD11B (p170); ?in same restriction fragment as LFA1A chr17_39776995_r_171 171 KRTAP9-9 NM_030975 INTRON chr17_62351608_y_171 171 DDX42 NM_007372 INTRON chr20_796077_y_171 171 C20orf55 NM_031424 UTR chr22_42059173_r_171 171 C22orf1 NM_001585 INTRON chr2_166725317_r_171 171 TAIP-2 NM_024969 INTRON chr2_230206234_r_171 171 FLJ20701 NM_017933 INTRON chr3_102295799_r_171 171 IMPG2 NM_016247 INTRON OMIM: 607056 IMPG2, IPM200 Interphotoreceptor matrix proteoglycan 2 chr5_43243735_y_171 171 MGC42105 NM_153361 UTR chr8_40476264_r_171 171 FLJ13842 NM_024645 INTRON chrX_2842458_r_171 171 DKFZp564I1922 NM_015419 INTRON chrX_66748492_y_171 171 STARD8 NM_014725 UTR chr11_117266991_y_172 172 SCN2B NM_004588 UTR OMIM: 601327 SCN2B Sodium channel, voltage-gated, type II, beta polypeptide MOUSE: 9(Scn2b) chr11_117266991_y_172 172 FXYD6 NM_022003 UTR OMIM: 606683 FXYD6 FXYD domain-containing ion transport regulator 6 chr15_43534328_y_172 172 FLJ39426 NM_173609 UTR chr15_67363424_y_172 172 MPRG NM_017705 UTR OMIM: 607781 MPRG Membrane progestin receptor, gamma chr16_20413943_y_172 172 FLJ20581 NM_017888 INTRON chr3_113382020_y_172 172 MOX2 NM_005944 INTRON OMIM: 155970 MOX2 MRC OX-2 antigen chr5_35710282_r_172 172 FLJ25395 NM_144722 INTRON chr6_157391900_y_172 172 ELD/OSA1 NM_175863 INTRON chr6_157391900_y_172 172 ELD/OSA1 NM_020732 INTRON chr7_136618006_r_172 172 DGKI NM_004717 INTRON OMIM: 604072 DGKI Diacylglycerol kinase, iota, 130-kD chr7_86146407_r_172 172 FLJ31340 NM_152748 UTR chrX_109832301_y_172 172 TRPC5 NM_012471 INTRON OMIM: 300334 TRPC5, TRP5 Transient receptor potential channel 5 chrX_23972910_y_172 172 PCYT1B NM_004845 INTRON chrX_66437014_y_172 172 OPHN1 NM_002547 INTRON OMIM: 300127 OPHN1 Oligophrenin-1 Mental retardation, X-linked, 60 (3) chr12_111527087_y_173 173 RPH3A NM_014954 UTR OMIM: 604881 RPH3AL, NOC2 Rabphilin 3A-like chr14_31400429_y_173 173 NPAS3 NM_022123 INTRON chr16_76336034_y_173 173 CASPR4 NM_033401 INTRON chr18_65696462_r_173 173 DNAM-1 NM_006566 INTRON chr19_35566953_y_173 173 KIAA0390 NM_014717 UTR chr19_7170524_r_173 173 INSR NM_000208 INTRON OMIM: 147671 INSRR, IRR Insulin receptor-related receptor chr20_36477883_y_173 173 C20orf132 NM_152503 INTRON chr22_35294738_y_173 173 CACNG2 NM_006078 INTRON OMIM: 602911 CACNG2 Calcium channel, voltage-dependent, gamma-2 subunit MOUSE: 15(Cacng2) chr2_49329411_y_173 173 FSHR NM_000145 INTRON OMIM: 136435 FSHR, ODG1 Follicle stimulating hormone receptor Premature ovarian failure, 233300 (3); Ovarian sex cord tumors (3);Twinning, diz chr2_49329411_y_173 173 FSHR NM_181446 INTRON OMIM: 136435 FSHR, ODG1 Follicle stimulating hormone receptor Premature ovarian failure, 233300 (3); Ovarian sex cord tumors (3);Twinning, diz chr5_102400499_r_173 173 PAM NM_000919 INTRON OMIM: 170270 PAM Peptidylglycine alpha-amidating monooxygenase MOUSE: 1(Pam) chr5_102400499_r_173 173 PAM NM_138766 INTRON OMIM: 170270 PAM Peptidylglycine alpha-amidating monooxygenase MOUSE: 1(Pam) chr5_102400499_r_173 173 PAM NM_138821 INTRON OMIM: 170270 PAM Peptidylglycine alpha-amidating monooxygenase MOUSE: 1(Pam) chr5_102400499_r_173 173 PAM NM_138822 INTRON OMIM: 170270 PAM Peptidylglycine alpha-amidating monooxygenase MOUSE: 1(Pam) chr7_90252059_y_173 173 PFTK1 NM_012395 INTRON chr11_12823502_y_174 174 TEAD1 NM_021961 INTRON chr12_32190987_y_174 174 BICD1 NM_001714 INTRON OMIM: 602204 BICD1 Bicaudal-D, Drosophila, homolog of, 1 second homolog on 9q chr18_19829503_r_174 174 FLJ33761 NM_153211 UTR chr1_181767971_y_174 174 C1orf21 NM_030806 INTRON chr1_220979574_r_174 174 TP53BP2 NM_005426 UTR OMIM: 602143 TP53BP2, ASPP2 Tumor protein p53-binding protein-2 chr3_134489687_r_174 174 BFSP2 NM_003571 INTRON OMIM: 603212 BFSP2, CP49, CP47 Beaded filament structural protein 2 (cytoskeletal protein, 49 kD) Cataract, juvenile-onset, 604219 (3); Cataract, congenital, 604219(3) chr5_61910103_y_174 174 IPO11 NM_016338 INTRON chr7_21573688_y_174 174 DNAH11 NM_003777 INTRON OMIM: 603339 DNAH11, DNAHC11 Dynein, axonemal, heavy chain-11 Situs inversus viscerum, 270100 (3); Kartagener syndrome, 244400 (3) chr7_83332447_r_174 174 SEMA3A NM_006080 INTRON chrX_108024597_y_174 174 FLJ22679 NM_032227 INTRON chr10_98590862_r_175 175 SLIT1 NM_003061 INTRON chr12_21972511_r_175 175 ABCC9 NM_020297 INTRON chr12_21972511_r_175 175 ABCC9 NM_005691 INTRON chr12_21972511_r_175 175 ABCC9 NM_020298 INTRON chr15_55016003_y_175 175 TCF12 NM_003205 INTRON OMIM: 600480 TCF12, HTF4 Transcription factor-12 (HTF4, helix-loop-helix transcriptionfactors-4) chr16_66662603_r_175 175 CA7 NM_005182 INTRON OMIM: 607640 SCA7, OPCA3 Ataxin 7 Spinocerebellar ataxia-7, 164500 (3) chr19_43402647_r_175 175 DPF1 NM_004647 INTRON chr19_56139991_y_175 175 KLK5 NM_012427 INTRON OMIM: 605643 KLK5, SCTE, KLKL2 Kallikrein 5 chr1_43736430_y_175 175 SIAT6 NM_006279 INTRON OMIM: 606494 SIAT6, ST3GALII Sialyltransferase 6 chr1_43736430_y_175 175 SIAT6 NM_174963 INTRON OMIM: 606494 SIAT6, ST3GALII Sialyltransferase 6 chr1_43736430_y_175 175 SIAT6 NM_174964 INTRON OMIM: 606494 SIAT6, ST3GALII Sialyltransferase 6 chr1_43736430_y_175 175 SIAT6 NM_174965 INTRON OMIM: 606494 SIAT6, ST3GALII Sialyltransferase 6 chr1_43736430_y_175 175 SIAT6 NM_174966 INTRON OMIM: 606494 SIAT6, ST3GALII Sialyltransferase 6 chr1_43736430_y_175 175 SIAT6 NM_174967 INTRON OMIM: 606494 SIAT6, ST3GALII Sialyltransferase 6 chr1_43736430_y_175 175 SIAT6 NM_174968 INTRON OMIM: 606494 SIAT6, ST3GALII Sialyltransferase 6 chr1_43736430_y_175 175 SIAT6 NM_174969 INTRON OMIM: 606494 SIAT6, ST3GALII Sialyltransferase 6 chr1_43736430_y_175 175 SIAT6 NM_174970 INTRON OMIM: 606494 SIAT6, ST3GALII Sialyltransferase 6 chr1_43736430_y_175 175 SIAT6 NM_174971 INTRON OMIM: 606494 SIAT6, ST3GALII Sialyltransferase 6 chr1_43736430_y_175 175 SIAT6 NM_174972 INTRON OMIM: 606494 SIAT6, ST3GALII Sialyltransferase 6 chr21_46779684_y_175 175 DIP2 NM_015151 INTRON OMIM: 607711 DIP2, KIAA0184 Disco-interacting protein 2, Drosophila, homolog of MOUSE: 10(Dip2) chr2_69750117_y_175 175 AAK1 NM_014911 INTRON chr5_170026298_r_175 175 KCNIP1 NM_014592 INTRON chr7_72879196_r_175 175 ELN NM_000501 INTRON OMIM: 606210 SEPN1, SELN, RSMD1 Selenoprotein N Muscular dystrophy, rigid spine, 1, 602771 (3) chr8_100328932_y_175 175 COH1 NM_017890 INTRON OMIM: 607817 COH1 COH1 gene Cohen syndrome, 216550 (3) chr8_100328932_y_175 175 COH1 NM_152564 INTRON OMIM: 607817 COH1 COH1 gene Cohen syndrome, 216550 (3) chr8_126281932_r_175 175 FLJ32440 NM_173685 INTRON chr8_2035218_y_175 175 MYOM2 NM_003970 INTRON OMIM: 603509 MYOM2 Myomesin 2 chr8_31568067_y_175 175 NRG1 NM_013962 INTRON OMIM: 142445 NRG1, HGL, HRGA, ARI Neuregulin 1 (heregulin, alpha, 45kD; ERBB2 p185-activator) {?Schizophrenia, susceptibility to}, 603013 (1) MOUSE: 7(Nrg1) chrX_104646789_r_175 175 FLJ10178 NM_018015 INTRON chr11_131965824_y_176 176 OPCML NM_002545 INTRON OMIM: 600632 OPCML Opioid-binding protein/cell adhesion molecule-like ?on 11q22-q23 MOUSE: 9(Obcam) chr12_116456079_y_176 176 FLJ25965 NM_173598 INTRON chr12_2156919_y_176 176 CACNA1C NM_000719 INTRON OMIM: 114205 CACNA1C, CACNL1A1, C Calcium channel, voltage-dependent, L type, alpha 1C subunit chr16_81313468_y_176 176 KIAA1694 NM_030629 INTRON chr1_119888882_r_176 176 NOTCH2 NM_024408 INTRON OMIM: 600275 NOTCH2 Notch, Drosophila, homolog of, 2 MOUSE: 3(Notch2) chr1_184157369_r_176 176 PLA2G4A NM_024420 INTRON OMIM: 600522 PLA2G4A, PLA2G4 Phospholipase A2, group IVA, cytosolic chr20_20271630_y_176 176 C20orf26 NM_015585 INTRON chr20_58895541_y_176 176 H17739 NM_080672 INTRON chr2_125565942_y_176 176 caspr5 NM_130773 INTRON chr2_125565942_y_176 176 caspr5 NM_138996 INTRON chr3_26653297_y_176 176 LRP15 NM_052953 UTR chr8_51446579_y_176 176 SNTG1 NM_018967 INTRON chrX_1257662_r_176 176 P2RY8 NM_178129 UTR chrY_1257662_r_176 176 P2RY8 NM_178129 UTR chr11_122533805_y_177 177 ASAM NM_024769 INTRON chr13_30148172_y_177 177 GREAT NM_130806 INTRON chr14_59910238_y_177 177 PRKCH NM_006255 INTRON OMIM: 605437 PRKCH, PKCL, PRKCL Protein kinase C, eta chr14_61852194_r_177 177 PPP2R5E NM_006246 INTRON OMIM: 601647 PPP2R5E Protein phosphatase-2, regulatory subunit B (B56), epsilon isoform chr16_10971478_y_177 177 MHC2TA NM_000246 INTRON OMIM: 600005 MHC2TA, C2TA MHC class II transactivator MHC class II deficiency, complementation group A, 209920 (3) chr17_4568412_y_177 177 MGC29671 NM_182538 INTRON chr19_48845543_r_177 177 PLAUR NM_002659 INTRON OMIM: 173391 PLAUR, URKR Plasminogen activator, urokinase, receptor chr1_238531439_r_177 177 RGS7 NM_002924 INTRON chr22_32442768_r_177 177 LARGE NM_004737 INTRON OMIM: 603590 LARGE Acetylglucosaminyltransferase-like protein ?Meningioma (2) chr22_32442768_r_177 177 LARGE NM_133642 INTRON OMIM: 603590 LARGE Acetylglucosaminyltransferase-like protein ?Meningioma (2) chr8_106502715_y_177 177 ZFPM2 NM_012082 INTRON OMIM: 603693 ZFPM2, FOG2 Zinc finger protein, multitype 2 (friend of GATA2) chrX_127597390_r_177 177 XPNPEP2 NM_003399 INTRON OMIM: 300145 XPNPEP2 X-prolyl aminopeptidase 2 (aminopeptidase P) chr10_34756042_r_178 178 PARD3 NM_019619 INTRON OMIM: 606745 PARD3, PAR3 Partitioning-defective protein 3, C. elegans, homolog of chr10_99067141_y_178 178 PI4KII NM_018425 INTRON chr11_66578586_y_178 178 SYT12 NM_177963 INTRON chr15_63998727_r_178 178 MEGF11 NM_032445 INTRON chr18_616865_r_178 178 CLUL1 NM_014410 INTRON chr1_85985694_y_178 178 COL24A1 NM_152890 INTRON chr22_35715007_r_178 178 TMPRSS6 NM_153609 INTRON chr2_230622105_r_178 178 DNER NM_139072 INTRON OMIM: 607299 DNER Delta-and notch-like egf-related receptor chr9_82998106_y_178 178 NTRK2 NM_006180 INTRON OMIM: 600456 NTRK2, TRKB Neurotrophic tyrosine kinase, receptor, type 2 chrX_100439247_r_178 178 NXF2 NM_022053 UTR OMIM: 300315 NXF2 Nuclear RNA export factor 2 chrX_100439247_r_178 178 NXF2 NM_017809 UTR OMIM: 300315 NXF2 Nuclear RNA export factor 2 chr10_20454956_r_179 179 TEM7R NM_032812 INTRON OMIM: 606827 TEM7R Tumor endothelial marker 7-related protein chr13_23080940_r_179 179 ATP12A NM_001676 INTRON OMIM: 182360 ATP12A, ATP1AL1 ATPase, H+/K+ transporting, nongastric, alpha polypeptide chr17_63119337_r_179 179 SMURF2 NM_022739 INTRON chr17_65514745_y_179 179 CACNG4 NM_014405 INTRON chr18_57312233_y_179 179 CDH20 NM_031891 INTRON OMIM: 605807 CDH20 Cadherin 20 chr1_173359754_r_179 179 COP1 NM_022457 INTRON OMIM: 608067 COP1 Constitutive photomorphogenesis protein, Arabidopsis, homolog of pseudogenes on chr. 3, 9, 18 chr4_66334535_r_179 179 EPHA5 NM_004439 INTRON chr4_66334535_r_179 179 EPHA5 NM_182472 INTRON chr5_36682041_y_179 179 SLC1A3 NM_004172 INTRON OMIM: 600111 SLC1A3, EAAT1 Solute carrier family 1 (glial high affinity glutamate transporter),member 3 MOUSE: 15(Eaat1) chr9_109034769_r_179 179 EDG2 NM_057159 INTRON chr9_109034769_r_179 179 EDG2 NM_001401 INTRON chr9_115198633_r_179 179 ASTN2 NM_014010 UTR chr10_101746004_r_180 180 PKD2L1 NM_016112 INTRON OMIM: 604532 PKD2L1, PKDL, PKD2L Polycystin L MOUSE: 19(Pkdl) chr14_35223270_r_180 180 SLC25A21 NM_030631 INTRON OMIM: 607571 SLC25A21, ODC Solute carrier family 25 (mitochondrial oxodicarbosylate carrier),member 21 chr3_160751400_r_180 180 SCHIP1 NM_014575 INTRON chr3_170472238_r_180 180 MDS1 NM_004991 INTRON OMIM: 600049 MDS1 Myelodysplasia syndrome-1 cen--EVI1--MDS1--EAP--tel Myelodysplasia syndrome-1 (3) chr3_32734083_y_180 180 FLJ12890 NM_015442 INTRON chr4_163282376_y_180 180 DKFZp566D234 NM_020116 INTRON chr7_102052397_y_180 180 MGC21636 NM_145032 INTRON chr9_66448801_y_180 180 PGM5 NM_021965 INTRON OMIM: 600981 PGM5 Phosphoglucomutase-5 chrX_66488882_r_180 180 OPHN1 NM_002547 INTRON OMIM: 300127 OPHN1 Oligophrenin-1 Mental retardation, X-linked, 60 (3) chr10_98675969_r_181 181 MGC14258 NM_032900 INTRON chr11_113643962_y_181 181 ZNF145 NM_006006 INTRON chr12_106748499_r_181 181 PRDM4 NM_012406 UTR OMIM: 605780 PRDM4, PFM1 PR domain-containing protein 4 chr14_69366784_y_181 181 PCNX NM_014982 INTRON chr15_79113381_y_181 181 FLJ38615 NM_173528 UTR chr17_9431124_r_181 181 STX8 NM_004853 INTRON OMIM: 604203 STX8 Syntaxin 8 chr1_70875635_r_181 181 PTGER3 NM_000957 INTRON OMIM: 176806 PTGER3, EP3 Prostaglandin E receptor 3, EP3 subtype MOUSE: 3(Ptger3) chr20_31427488_r_181 181 HCK NM_002110 INTRON OMIM: 142370 HCK Hemopoietic cell kinase chr22_29443145_y_181 181 OSBP2 NM_030758 INTRON OMIM: 606729 OSBP2, ORP4, KIAA166 Oxysterol-binding protein 2 chr3_13885166_r_181 181 WNT7A NM_004625 INTRON OMIM: 601570 WNT7A Wingless-type MMTV integration site family, member 7A chr6_109405651_r_181 181 PA26 NM_014454 INTRON OMIM: 606103 PA26 p53-activated gene 26 MOUSE: 4(Pa26) chr6_160914489_y_181 181 LPA NM_005577 INTRON OMIM: 603099 LPAATA Lysophosphatidic acid acyltransferase-alpha chr6_160914489_y_181 181 LPA NM_005577 INTRON OMIM: 603099 LPAATA Lysophosphatidic acid acyltransferase-alpha chr6_160914489_y_181 181 LPA NM_005577 INTRON OMIM: 603099 LPAATA Lysophosphatidic acid acyltransferase-alpha chr7_150861812_r_181 181 PRKAG2 NM_016203 INTRON OMIM: 602743 PRKAG2, WPWS Protein kinase, AMP-activated, noncatalytic, gamma-2 Wolff-Parkinson-White syndrome, 194200 (3); Cardiomyopathy,hypertrophic, with WP chr7_20495704_y_181 181 LOC340273 NM_178559 INTRON chr9_72621514_r_181 181 RORB NM_006914 INTRON OMIM: 601972 RORB, RZRB RAR-related orphan receptor B MOUSE: 4(Rorb) chrX_10554053_y_181 181 ARHGAP6 NM_013423 INTRON OMIM: 300118 ARHGAP6 Rho GTPase-activating protein-6 chrX_10554053_y_181 181 ARHGAP6 NM_001174 INTRON OMIM: 300118 ARHGAP6 Rho GTPase-activating protein-6 chrX_10554053_y_181 181 ARHGAP6 NM_013427 INTRON OMIM: 300118 ARHGAP6 Rho GTPase-activating protein-6 chrX_10554053_y_181 181 ARHGAP6 NM_013422 INTRON OMIM: 300118 ARHGAP6 Rho GTPase-activating protein-6 chrX_10554053_y_181 181 ARHGAP6 NM_006125 INTRON OMIM: 300118 ARHGAP6 Rho GTPase-activating protein-6 chrX_28116637_y_181 181 IL1RAPL1 NM_014271 UTR chr10_28004311_y_182 182 MGC39616 NM_173576 INTRON chr11_122527279_y_182 182 ASAM NM_024769 INTRON chr13_111664041_y_182 182 MCF2L NM_024979 INTRON chr15_42308353_r_182 182 H63 NM_138423 INTRON chr15_42308353_r_182 182 H63 NM_177974 INTRON chr16_81616806_y_182 182 PLCG2 NM_002661 INTRON OMIM: 600220 PLCG2 Phospholipase C, gamma 2 (phosphatidylyinositol-specific) MOUSE: 8(Plcg2) chr18_45171352_r_182 182 FLJ20071 NM_017653 INTRON chr19_60402785_r_182 182 PTPRH NM_002842 INTRON OMIM: 602510 PTPRH Protein tyrosine phosphatase, receptor type, H chr1_234322026_y_182 182 RYR2 NM_001035 INTRON OMIM: 180902 RYR2, VTSIP Ryanodine receptor-2 (cardiac) Ventricular tachycardia, stress-induced polymorphic, 604772 (3);Arrhythmogenic r MOUSE: 13(Ryr2) chr20_32304989_y_182 182 SPAG4L NM_080675 INTRON chr6_76679560_y_182 182 IMPG1 NM_001563 INTRON OMIM: 602870 IMPG1, IPM150 Interphotoreceptor matrix proteoglycan-1 chr8_3316472_y_182 182 CSMD1 NM_033225 INTRON OMIM: 608397 CSMD1, KIAA1890 Cub and Sushi multiple domains 1 chrX_16048201_r_182 182 CTPS2 NM_175859 INTRON OMIM: 300380 CTPS2 Cytidine 5-prime triphosphate synthetase 2 chrX_16048201_r_182 182 CTPS2 NM_019857 INTRON OMIM: 300380 CTPS2 Cytidine 5-prime triphosphate synthetase 2 chr11_83750868_r_183 183 DLG2 NM_001364 INTRON OMIM: 603583 DLG2 Discs large, Drosophila, homolog of, 2(channel-associated protein of synapses, 1 chr12_5882039_r_183 183 C12orf3 NM_020373 INTRON chr15_67308998_y_183 183 MPRG NM_017705 UTR OMIM: 607781 MPRG Membrane progestin receptor, gamma chr15_80684997_y_183 183 FLJ22795 NM_025084 UTR chr16_23959913_y_183 183 PRKCB1 NM_002738 INTRON OMIM: 176970 PRKCB1, PKCB Protein kinase C, beta 1 polypeptide chr16_50401627_y_183 183 NKD1 NM_033119 INTRON chr19_3859623_y_183 183 KIAA1872 NM_033064 INTRON chr19_3859623_y_183 183 FLJ10374 NM_018074 UTR chr20_18007878_r_183 183 ZNF339 NM_021220 INTRON chr21_39108254_r_183 183 ETS2 NM_005239 INTRON OMIM: 164740 ETS2 Oncogene ETS-2 proximal q22.3 MOUSE: 16(Ets2) chr6_46891792_y_183 183 GPR116 NM_015234 INTRON chr7_2724591_r_183 183 CARD11 NM_032415 INTRON chrX_98880053_y_183 183 NOX1 NM_007052 INTRON OMIM: 602100 PKNOX1 PBX/knotted 1 homeo box 1 MOUSE: 17(Pknox1) chrX_98880053_y_183 183 NOX1 NM_013954 INTRON OMIM: 602100 PKNOX1 PBX/knotted 1 homeo box 1 MOUSE: 17(Pknox1) chrX_98880053_y_183 183 NOX1 NM_013955 INTRON OMIM: 602100 PKNOX1 PBX/knotted 1 homeo box 1 MOUSE: 17(Pknox1) chr12_39396304_y_184 184 CNTN1 NM_001843 UTR OMIM: 600016 CNTN1 Contactin 1 chr12_39396304_y_184 184 CNTN1 NM_175038 UTR OMIM: 600016 CNTN1 Contactin 1 chr16_80942374_y_184 184 PKD1L2 NM_052892 INTRON chr1_228932824_y_184 184 DISC1 NM_018662 INTRON OMIM: 605210 DISC1 Disrupted in schizophrenia 1 Schizophrenia, 181500 (2) MOUSE: 8(Disc1) chr6_144661719_y_184 184 UTRN NM_007124 INTRON OMIM: 128240 UTRN, DMDL, DRP1 Utrophin (homologous to dystrophin) near dy in mouse MOUSE: 10(Dmdl) chr7_38390615_r_184 184 AMPH NM_001635 INTRON OMIM: 601248 BIN1, AMPHL Box-dependent MYC-interacting protein-1 (amphiphysin-like) MOUSE: 18(Bin1) chr7_38390615_r_184 184 AMPH NM_139316 INTRON OMIM: 601248 BIN1, AMPHL Box-dependent MYC-interacting protein-1 (amphiphysin-like) MOUSE: 18(Bin1) chr10_101739285_r_185 185 PKD2L1 NM_016112 INTRON OMIM: 604532 PKD2L1, PKDL, PKD2L Polycystin L MOUSE: 19(Pkdl) chr10_113826094_y_185 185 FACL5 NM_016234 INTRON OMIM: 605677 FACL5, ACS5 Fatty acid CoA ligase, long-chain 5 chr12_49278769_y_185 185 FLJ34278 NM_173602 INTRON chr17_28306315_y_185 185 SSH2 NM_033389 INTRON OMIM: 606779 SSH2, KIAA1725 Slingshot, drosophila, homolog of, 2 chr17_77623634_y_185 185 FLJ21865 NM_022759 INTRON chr1_57388930_r_185 185 DAB1 NM_021080 UTR OMIM: 603448 DAB1 Disabled, Drosophila, homolog 1 MOUSE: 4(Dab1) chr20_8296436_r_185 185 PLCB1 NM_015192 INTRON chr2_102433408_y_185 185 IL1RL2 NM_003854 INTRON OMIM: 604512 IL1RL2, IL1RRP2 Interleukin 1 receptor-like 2 chr6_146572544_y_185 185 GRM1 NM_000838 INTRON OMIM: 604473 GRM1, MGLUR1, GRM1A Glutamate receptor, metabotropic, 1 chr7_78196972_y_185 185 AIP1 NM_012301 INTRON OMIM: 608074 PDCD6IP, AIP1, ALIX, Programmed cell death 6-interacting protein chr9_110272587_r_185 185 DKFZP761E1824 NM_022486 INTRON chr13_99650635_y_186 186 VGCNL1 NM_052867 INTRON chr17_49225899_y_186 186 ABCC3 NM_003786 INTRON OMIM: 604323 ABCC3, CMOAT2, MRP3, ATP-binding cassette, sub-family C, member 3 chr17_49225899_y_186 186 ABCC3 NM_020037 INTRON OMIM: 604323 ABCC3, CMOAT2, MRP3, ATP-binding cassette, sub-family C, member 3 chr17_49225899_y_186 186 ABCC3 NM_020038 UTR OMIM: 604323 ABCC3, CMOAT2, MRP3, ATP-binding cassette, sub-family C, member 3 chr1_39026320_y_186 186 MACF1 NM_012090 INTRON chr1_48433369_r_186 186 FLJ14442 NM_032785 INTRON chr2_125440783_y_186 186 caspr5 NM_130773 INTRON chr2_125440783_y_186 186 caspr5 NM_138996 INTRON chr2_216468448_r_186 186 FN1 NM_002026 INTRON OMIM: 135600 FN1 Fibronectin-1 ?Ehlers-Danlos syndrome, type X, 225310 (1) MOUSE: 1(Fn1) chr3_13873328_r_186 186 WNT7A NM_004625 INTRON OMIM: 601570 WNT7A Wingless-type MMTV integration site family, member 7A chr4_46937107_y_186 186 COX7B2 NM_130902 UTR chr6_107082617_r_186 186 RTN4IP1 NM_032730 INTRON chr7_70724782_r_186 186 CALN1 NM_031468 INTRON chr9_125121092_y_186 186 RALGPS1A NM_014636 INTRON chr9_33929720_r_186 186 UBAP2 NM_018449 INTRON chr9_33929720_r_186 186 UBAP2 NM_020867 INTRON chr9_33929720_r_186 186 UBAP2 NM_148171 UTR chr12_127745962_y_187 187 FLJ31978 NM_144669 INTRON chr14_101088990_y_187 187 RCOR NM_015156 INTRON OMIM: 607675 RCOR, COREST, KIAA00 REST corepressor chr16_56377461_r_187 187 MT4 NM_032935 INTRON OMIM: 606598 GDAP1, CMT4A, CMT2K, Ganglioside-induced differentiation-associated protein 1 Charcot-Marie-Tooth disease, type 4A, 214400 (3);Charcot-Marie-Tooth disease, ty chr19_53211458_y_187 187 ELSPBP1 NM_022142 INTRON chr1_233651540_y_187 187 EDARADD NM_145861 INTRON OMIM: 606603 EDARADD EDAR-associated death domain MOUSE: 13(Edaradd) chr1_233651540_y_187 187 EDARADD NM_080738 INTRON OMIM: 606603 EDARADD EDAR-associated death domain MOUSE: 13(Edaradd) chr7_110584741_r_187 187 IMMP2L NM_032549 INTRON OMIM: 605977 IMP2, IMMP2L Inner mitochondrial membrane peptidase, subunit 2, yeast, homolog of chr8_40476436_r_187 187 FLJ13842 NM_024645 INTRON chr8_40621086_y_187 187 FLJ13842 NM_024645 INTRON chr11_17436086_y_188 188 ABCC8 NM_000352 INTRON OMIM: 600509 ABCC8, SUR, PHHI, SU ATP-binding cassette, subfamily C, member 8 (sulfonylurea receptor) Persistent hyperinsulinemic hypoglycemia of infancy, 256450 (3) chr11_3800256_y_188 188 FRAG1 NM_014489 INTRON chr14_77684070_y_188 188 NRXN3 NM_004796 INTRON OMIM: 600567 NRXN3 Neurexin 3 chr15_57527702_y_188 188 MGC26690 NM_152450 INTRON chr19_46403070_y_188 188 CYP2S1 NM_030622 INTRON chr2_102023517_y_188 188 MAP4K4 NM_004834 INTRON chr2_102023517_y_188 188 MAP4K4 NM_145686 INTRON chr2_102023517_y_188 188 MAP4K4 NM_145687 INTRON chr2_114571515_r_188 188 FLJ22004 NM_025181 INTRON chr2_173993004_r_188 188 CGEF2 NM_007023 INTRON chr6_133093935_r_188 188 dJ55C23.6 NM_052831 INTRON chr8_11430097_r_188 188 BLK NM_001715 UTR OMIM: 191305 BLK BLK nonreceptor tyrosine kinase MOUSE: 14(Blk) chr9_119156943_r_188 188 C5 NM_001735 INTRON OMIM: 176844 PSMA5, PSC5 Proteasome component 5 chr9_121828313_r_188 188 KIAA1608 NM_024820 INTRON chr10_33121322_r_189 189 FLJ13031 NM_024688 INTRON chr19_54392328_y_189 189 TRPM4 NM_017636 INTRON OMIM: 606936 TRPM4 Transient receptor potential cation channel, subfamily M, member 4 chr4_15102691_r_189 189 C1QTNF7 NM_031911 UTR chr7_93129830_r_189 189 TFPI2 NM_006528 INTRON OMIM: 600033 TFPI2 Tissue factor pathway inhibitor-2 chr12_14728701_y_190 190 GUCY2C NM_004963 INTRON OMIM: 601330 GUCY2C, GUC2C Guanylate cyclase 2C (heat stable enterotoxin receptor) MOUSE: 6(Gucy2c) chr16_47408086_r_190 190 PHKB NM_000293 INTRON OMIM: 172490 PHKB Phosphorylase kinase, beta polypeptide Phosphorylase kinase deficiency of liver and muscle, autosomalrecessive, 261750 chr17_79339233_y_190 190 raptor NM_020761 INTRON chr18_7762324_y_190 190 PTPRM NM_002845 INTRON OMIM: 176888 PTPRM, PTPRL1, RPTPM Protein tyrosine phosphatase, receptor type, mu polypeptide chr1_118782241_r_190 190 TBX15 NM_152380 INTRON OMIM: 604127 TBX15 T-box 15 MOUSE: 3(Tbx15) chr1_59326584_y_190 190 FLJ10986 NM_018291 INTRON chr2_163807868_y_190 190 KCNH7 NM_033272 INTRON chr2_163807868_y_190 190 KCNH7 NM_173162 INTRON chr2_50479055_y_190 190 NRXN1 NM_138735 INTRON OMIM: 600565 NRXN1 Neurexin 1 chr2_50479055_y_190 190 NRXN1 NM_004801 INTRON OMIM: 600565 NRXN1 Neurexin 1 chr3_185069872_r_190 190 ABCC5 NM_005688 UTR OMIM: 605251 ABCC5, MRP5, MOATC ATP-binding cassette, subfamily C, member 5 chr4_176720365_r_190 190 ADAM29 NM_021780 INTRON OMIM: 604778 ADAM29 A disintegrin and metalloproteinase domain 29 chr6_69736429_y_190 190 BAI3 NM_001704 INTRON OMIM: 602684 BAI3 Brain-specific angiogenesis inhibitor-3 chr7_47644919_y_190 190 PKD1L1 NM_138295 INTRON chr7_99947860_y_190 190 ZAN NM_003386 INTRON OMIM: 602372 ZAN Zonadhesin MOUSE: 5(Zan) chr7_99947860_y_190 190 ZAN NM_173055 INTRON OMIM: 602372 ZAN Zonadhesin MOUSE: 5(Zan) chr7_99947860_y_190 190 ZAN NM_173056 INTRON OMIM: 602372 ZAN Zonadhesin MOUSE: 5(Zan) chr7_99947860_y_190 190 ZAN NM_173057 INTRON OMIM: 602372 ZAN Zonadhesin MOUSE: 5(Zan) chr7_99947860_y_190 190 ZAN NM_173058 INTRON OMIM: 602372 ZAN Zonadhesin MOUSE: 5(Zan) chr7_99947860_y_190 190 ZAN NM_173059 INTRON OMIM: 602372 ZAN Zonadhesin MOUSE: 5(Zan) chr9_128321962_y_190 190 FREQ NM_014286 INTRON OMIM: 603315 FREQ, NCS1 Frequenin, Drosophila, homolog of chrX_66404061_r_190 190 OPHN1 NM_002547 INTRON OMIM: 300127 OPHN1 Oligophrenin-1 Mental retardation, X-linked, 60 (3) chrX_69255363_r_190 190 NLGN3 NM_018977 INTRON OMIM: 300336 NLGN3 Neuroligin 3 Autism, X-linked, 300425 (3); Asperger syndrome, 300425 (3) chr11_117188501_r_191 191 DSCAML1 NM_020693 INTRON chr11_117188501_r_191 191 SCN2B NM_004588 UTR OMIM: 601327 SCN2B Sodium channel, voltage-gated, type II, beta polypeptide MOUSE: 9(Scn2b) chr14_87967508_y_191 191 CHES1 NM_005197 UTR OMIM: 602628 CHES1 Checkpoint suppressor 1 chr16_31350214_y_191 191 ITGAM NM_000632 INTRON OMIM: 120980 ITGAM, CR3A, CD11B, Integrin, alpha-M (complement component receptor-3, alpha; antigenCD11B (p170); ?in same restriction fragment as LFA1A chr20_44879044_r_191 191 WFDC8 NM_130896 INTRON chr20_44879044_r_191 191 WFDC8 NM_181510 INTRON chr22_21796726_r_191 191 RTDR1 NM_014433 INTRON OMIM: 605663 RTDR1 Rhabdoid tumor deletion region protein 1 chr22_31292950_y_191 191 SYN3 NM_003490 INTRON OMIM: 602705 SYN3 Synapsin III ?relation to schizophrenia chr22_31292950_y_191 191 SYN3 NM_133632 INTRON OMIM: 602705 SYN3 Synapsin III ?relation to schizophrenia chr22_31292950_y_191 191 SYN3 NM_133633 INTRON OMIM: 602705 SYN3 Synapsin III ?relation to schizophrenia chr2_135536864_r_191 191 DKFZP566N034 NM_030923 INTRON chr3_130499344_y_191 191 WDR10 NM_018262 INTRON OMIM: 606045 WDR10 WD repeat-containing protein 10 chr3_130499344_y_191 191 WDR10 NM_052985 INTRON OMIM: 606045 WDR10 WD repeat-containing protein 10 chr3_130499344_y_191 191 WDR10 NM_052989 INTRON OMIM: 606045 WDR10 WD repeat-containing protein 10 chr3_130499344_y_191 191 WDR10 NM_052990 INTRON OMIM: 606045 WDR10 WD repeat-containing protein 10 chr4_62726023_y_191 191 LPHN3 NM_015236 INTRON chr6_13517294_r_191 191 GFOD1 NM_018988 INTRON chrX_102599248_y_191 191 IL1RAPL2 NM_017416 UTR OMIM: 300277 IL1RAPL2 Interleukin 1 receptor accessory protein-like 2 chr12_123675052_r_192 192 SCARB1 NM_005505 INTRON OMIM: 601040 SCARB1, CD36L1, CLA1 Scavenger receptor class B, member 1(CD36 antigen-like 1) chr12_91782771_r_192 192 EEA1 NM_003566 INTRON chr19_3322850_y_192 192 NFIC NM_005597 INTRON OMIM: 600729 NFIC Nuclear factor I/C (CCAAT-binding transcription factor) order: cen-NFIX-NFIC-tel MOUSE: 10(Nfic) chr22_24668925_y_192 192 MYO18B NM_032608 INTRON OMIM: 607295 MYO18B Myosin XVIIIB chr4_66445072_r_192 192 EPHA5 NM_004439 INTRON chr4_66445072_r_192 192 EPHA5 NM_182472 INTRON chr7_70039082_y_192 192 WBSCR17 NM_022479 INTRON chr7_78377306_r_192 192 AIP1 NM_012301 INTRON OMIM: 608074 PDCD6IP, AIP1, ALIX, Programmed cell death 6-interacting protein chrX_149504169_r_192 192 FATE NM_033085 INTRON chr10_113879664_y_193 193 VTI1A NM_145206 INTRON chr13_90877348_r_193 193 GPC5 NM_004466 INTRON OMIM: 602446 GPC5 Glypican 5 chr16_1282515_y_193 193 TPSG1 NM_012467 UTR chr16_56375975_r_193 193 MT4 NM_032935 INTRON OMIM: 606598 GDAP1, CMT4A, CMT2K, Ganglioside-induced differentiation-associated protein 1 Charcot-Marie-Tooth disease, type 4A, 214400 (3);Charcot-Marie-Tooth disease, ty chr17_46756919_y_193 193 SCAP1 NM_003726 INTRON OMIM: 604969 SCAP1, SKAP55 SRC kinase-associated phosphoprotein 1, 55kD chr18_3150011_y_193 193 MYOM1 NM_003803 INTRON chr19_19857026_y_193 193 ZNF253 NM_021047 INTRON OMIM: 606954 ZNF253 Zinc finger protein 253 chr2_170138915_r_193 193 RDHL NM_005771 UTR chr3_12771429_y_193 193 FLJ11036 NM_018306 UTR chrX_127591100_r_193 193 XPNPEP2 NM_003399 INTRON OMIM: 300145 XPNPEP2 X-prolyl aminopeptidase 2 (aminopeptidase P) chr10_70033609_y_194 194 DDX50 NM_024045 INTRON chr12_116114223_y_194 194 NOS1 NM_000620 INTRON OMIM: 163731 NOS1 Nitric oxide synthase 1, neuronal MOUSE: 5(Nos1) chr1_180598250_r_194 194 NMNAT2 NM_015039 INTRON chr5_93283071_r_194 194 DKFZP564D172 NM_032042 INTRON chr9_67708830_r_194 194 APBA1 NM_001163 UTR OMIM: 602414 APBA1, X11 Amyloid beta A4 precursor protein-binding, family A, member 1 chr11_116239558_y_195 195 APOC3 NM_000040 INTRON OMIM: 107720 APOC3 Apolipoprotein C-III 2.6kb 3' to APOA1 Hypertriglyceridemia (3) chr11_991117_y_195 195 AP2A2 NM_012305 INTRON chr18_3176725_r_195 195 MYOM1 NM_003803 INTRON chr1_27184513_y_195 195 KIAA1037 NM_015023 UTR chr3_116900774_y_195 195 LSAMP NM_002338 INTRON OMIM: 603241 LSAMP, LAMP Limbic system-associated membrane protein MOUSE: 16(Lsamp) chr11_100461947_y_196 196 PGR NM_000926 INTRON OMIM: 608197 PGRPIA Peptidoglycan recognition protein, intermediate, alpha chr11_127885786_r_196 196 ETS1 NM_005238 INTRON OMIM: 602011 ST11, PETS1 Suppression of tumorigenicity 11, pancreas ?Pancreatic endocrine tumors (1) chr14_50570366_r_196 196 CGI-99 NM_016039 UTR chr18_42551613_y_196 196 SIAT8E NM_013305 INTRON OMIM: 607162 SIAT8E Sialyltransferase 8E chr1_94054258_y_196 196 ABCA4 NM_000350 INTRON OMIM: 601691 ABCA4, ABCR, STGD1, ATP-binding transporter, retina-specific Stargardt disease-1, 248200 (3); Retinitis pigmentosa-19, 601718 (3);Cone-rod dy chr2_60708869_r_196 196 BCL11A NM_018014 INTRON OMIM: 606557 BCL11A, CTIP1, EVI9, B-cell CLL/lymphoma 11A chr2_60708869_r_196 196 BCL11A NM_138552 INTRON OMIM: 606557 BCL11A, CTIP1, EVI9, B-cell CLL/lymphoma 11A chr2_60708869_r_196 196 BCL11A NM_138553 INTRON OMIM: 606557 BCL11A, CTIP1, EVI9, B-cell CLL/lymphoma 11A chr2_60708869_r_196 196 BCL11A NM_138559 INTRON OMIM: 606557 BCL11A, CTIP1, EVI9, B-cell CLL/lymphoma 11A chr2_60708869_r_196 196 BCL11A NM_022893 INTRON OMIM: 606557 BCL11A, CTIP1, EVI9, B-cell CLL/lymphoma 11A chr3_89178419_r_196 196 EPHA3 NM_005233 INTRON OMIM: 179611 EPHA3, ETK1, HEK Ephrin receptor EphA3 (human embryo kinase 1) chr3_89178419_r_196 196 EPHA3 NM_182644 INTRON OMIM: 179611 EPHA3, ETK1, HEK Ephrin receptor EphA3 (human embryo kinase 1) chr6_36695895_y_196 196 CDKN1A NM_000389 UTR OMIM: 116899 CDKN1A, WAF1, CIP1, Cyclin-dependent kinase inhibitor 1A (p21, Cip1) MOUSE: 17(Waf1) chr6_36695895_y_196 196 CDKN1A NM_078467 UTR OMIM: 116899 CDKN1A, WAF1, CIP1, Cyclin-dependent kinase inhibitor 1A (p21, Cip1) MOUSE: 17(Waf1) chr6_46822086_r_196 196 MEP1A NM_005588 INTRON OMIM: 600388 MEP1A Meprin A, alpha MOUSE: 17(Mep1a) chr9_19626251_y_196 196 SLC24A2 NM_020344 INTRON chr9_69403648_r_196 196 TRPM3 NM_024971 INTRON chr10_22010716_y_197 197 MLLT10 NM_004641 INTRON chr21_18659692_y_197 197 PRSS7 NM_002772 INTRON OMIM: 606635 PRSS7, ENTK Protease, serine, 7 (enterokinase) Enterokinase deficiency, 226200 (3) chr5_145372203_y_197 197 FLJ23654 NM_152550 INTRON chrX_31831878_r_197 197 DMD NM_004007 INTRON OMIM: 605512 ELOVL4, ADMD, STGD2, Elongation of very long chain fatty acids 4 Stargardt disease 3, 600110 (3); Macular dystrophy, autosomaldominant, chromosom chrX_31831878_r_197 197 DMD NM_004009 INTRON OMIM: 605512 ELOVL4, ADMD, STGD2, Elongation of very long chain fatty acids 4 Stargardt disease 3, 600110 (3); Macular dystrophy, autosomaldominant, chromosom chrX_31831878_r_197 197 DMD NM_004010 INTRON OMIM: 605512 ELOVL4, ADMD, STGD2, Elongation of very long chain fatty acids 4 Stargardt disease 3, 600110 (3); Macular dystrophy, autosomaldominant, chromosom chrX_31831878_r_197 197 DMD NM_004006 INTRON OMIM: 605512 ELOVL4, ADMD, STGD2, Elongation of very long chain fatty acids 4 Stargardt disease 3, 600110 (3); Macular dystrophy, autosomaldominant, chromosom chrX_31831878_r_197 197 DMD NM_000109 INTRON OMIM: 605512 ELOVL4, ADMD, STGD2, Elongation of very long chain fatty acids 4 Stargardt disease 3, 600110 (3); Macular dystrophy, autosomaldominant, chromosom chr15_80496315_r_198 198 FLJ22795 NM_025084 UTR chr15_83162627_y_198 198 SLC28A1 NM_004213 INTRON OMIM: 606207 SLC28A1, CNT1 Solute carrier family 28 (sodium-coupled nucleoside transporter),member 1 chr1_53482401_r_198 198 FLJ36155 NM_147193 UTR chr1_70816834_y_198 198 PTGER3 NM_000957 INTRON OMIM: 176806 PTGER3, EP3 Prostaglandin E receptor 3, EP3 subtype MOUSE: 3(Ptger3) chr1_74287200_y_198 198 CARK NM_015978 INTRON OMIM: 605060 CARKL Carbohydrate kinase-like chr6_152957071_r_198 198 SYNE1 NM_033071 INTRON chr9_20711867_y_198 198 FLJ20375 NM_017794 INTRON chrX_37176092_y_198 198 RPGR NM_000328 INTRON OMIM: 605446 RPGRIP1, LCA6, CORD9 Retinitis pigmentosa GTPase regulator-interacting protein Leber congenital amaurosis, 204000 (3); Cone-rod dystrophy 9,608194 (3) chr10_35573248_r_199 199 CFP1 NM_181698 UTR chr14_77235027_y_199 199 NRXN3 NM_004796 INTRON OMIM: 600567 NRXN3 Neurexin 3 chr1_18100519_y_199 199 MGC15730 NM_032880 INTRON chr3_89181699_y_199 199 EPHA3 NM_005233 INTRON OMIM: 179611 EPHA3, ETK1, HEK Ephrin receptor EphA3 (human embryo kinase 1) chr3_89181699_y_199 199 EPHA3 NM_182644 INTRON OMIM: 179611 EPHA3, ETK1, HEK Ephrin receptor EphA3 (human embryo kinase 1) chr4_94828329_y_199 199 GRID2 NM_001510 INTRON OMIM: 602368 GRID2 Glutamate receptor, ionotropic, delta-2 MOUSE: 6(Grid2) chr6_20717425_y_199 199 CDKAL1 NM_017774 INTRON chr7_131664048_y_199 199 DKFZp434G0625 NM_181775 UTR chr7_36000257_r_199 199 KIAA1706 NM_030636 INTRON chr10_115112137_y_200 200 CASP7 NM_033340 UTR OMIM: 601761 CASP7, MCH3 Caspase 7, apoptosis-related cysteine protease chr10_115112137_y_200 200 CASP7 NM_001227 UTR OMIM: 601761 CASP7, MCH3 Caspase 7, apoptosis-related cysteine protease chr10_115112137_y_200 200 CASP7 NM_033339 UTR OMIM: 601761 CASP7, MCH3 Caspase 7, apoptosis-related cysteine protease chr10_115112137_y_200 200 CASP7 NM_033338 UTR OMIM: 601761 CASP7, MCH3 Caspase 7, apoptosis-related cysteine protease chr1_39744899_r_200 200 IPT NM_017646 INTRON OMIM: 607380 MIPT3 Microtubule-interacting protein associated with TRAF3 chr3_19325147_y_200 200 KCNH8 NM_144633 INTRON chr4_36055071_r_200 200 CENTD1 NM_139182 INTRON OMIM: 606645 CENTD1, ARAP2, KIAA0 Centaurin, delta-1 chr4_36055071_r_200 200 CENTD1 NM_015230 INTRON OMIM: 606645 CENTD1, ARAP2, KIAA0 Centaurin, delta-1 chr11_105042798_r_201 201 GRIA4 NM_000829 INTRON OMIM: 138246 GRIA4, GLUR4 Glutamate receptor, ionotropic, AMPA 4 MOUSE: 9(Glur4) chr12_108777029_r_201 201 GLTP NM_016433 INTRON chr13_100676954_r_201 201 FGF14 NM_175929 INTRON OMIM: 601515 FGF14, FHF4 Fibroblast growth factor-14 Cerebellar ataxia, autosomal dominant, FGF14-related (3) MOUSE: 14(Fhf4) chr2_122353028_r_201 201 CLASP1 NM_015282 INTRON OMIM: 605852 CLASP1, KIAA0622 CLIP-associated protein 1 chr2_74446060_y_201 201 SLC4A5 NM_133478 INTRON OMIM: 606757 SLC4A5, NBC4 Solute carrier family 4, sodium bicarbonate cotransporter, member 5 chr2_74446060_y_201 201 SLC4A5 NM_133479 INTRON OMIM: 606757 SLC4A5, NBC4 Solute carrier family 4, sodium bicarbonate cotransporter, member 5 chr2_74446060_y_201 201 SLC4A5 NM_021196 INTRON OMIM: 606757 SLC4A5, NBC4 Solute carrier family 4, sodium bicarbonate cotransporter, member 5 chr2_74446060_y_201 201 SLC4A5 NM_033323 INTRON OMIM: 606757 SLC4A5, NBC4 Solute carrier family 4, sodium bicarbonate cotransporter, member 5 chr4_21281182_r_201 201 KCNIP4 NM_147182 UTR OMIM: 608182 KCNIP4, KCHIP4 Kv channel-interacting protein 4 chr5_172540319_y_201 201 LOC153222 NM_153607 INTRON chr5_79121905_y_201 201 CMYA5 NM_153610 INTRON chrX_134168297_y_201 201 GPR112 NM_153834 INTRON chrX_2286616_r_201 201 XG NM_175569 INTRON OMIM: 600315 TNFRSF4, TXGP1L, OX4 Tumor necrosis factor receptor superfamily, member 4 MOUSE: 4(Ox40) chr22_24537812_y_202 202 MYO18B NM_032608 INTRON OMIM: 607295 MYO18B Myosin XVIIIB chr2_128499756_r_202 202 PROC NM_000312 UTR OMIM: 176860 PROC Protein C (inactivator of coagulation factors Va and VIIIa) Thrombophilia due to protein C deficiency (3); Purpura fulminans,neonatal (1) chr2_128499756_r_202 202 GPR17 NM_005291 UTR OMIM: 603071 GPR17 G protein-coupled receptor-17 chr2_128499756_r_202 202 LIMS2 NM_017980 INTRON chr3_2304286_r_202 202 CNTN4 NM_175607 UTR OMIM: 607280 CNTN4 Contactin 4 chr6_46630655_y_202 202 CYP39A1 NM_016593 INTRON OMIM: 605994 CYP39A1 Cytochrome P450, subfamily XXXIXA (oxysterol 7-alpha-hydroxylase),polypeptide 1 MOUSE: 17(Cyp39a1) chrX_84232239_y_202 202 DACH2 NM_053281 INTRON chr15_80882907_r_203 203 FLJ22795 NM_025084 UTR chr1_238425400_r_203 203 RGS7 NM_002924 INTRON chr22_24999350_r_203 203 SEZ6L NM_021115 INTRON OMIM: 607021 SEZ6L Seizure-related 6-like chr22_25069024_r_203 203 SEZ6L NM_021115 INTRON OMIM: 607021 SEZ6L Seizure-related 6-like chr2_95197324_r_203 203 MAL NM_002371 INTRON OMIM: 188860 MAL T-lymphocyte maturation-associated protein chr2_95197324_r_203 203 MAL NM_022438 INTRON OMIM: 188860 MAL T-lymphocyte maturation-associated protein chr2_95197324_r_203 203 MAL NM_022439 INTRON OMIM: 188860 MAL T-lymphocyte maturation-associated protein chr2_95197324_r_203 203 MAL NM_022440 INTRON OMIM: 188860 MAL T-lymphocyte maturation-associated protein chr4_186293349_y_203 203 FLJ33167 NM_152683 INTRON chr6_136758380_r_203 203 MAP7 NM_003980 INTRON OMIM: 604108 MAP7, EMAP115 Microtubule-associated protein-7 MOUSE: 10(Map7) chr8_131815590_y_203 203 ADCY8 NM_001115 INTRON OMIM: 103070 ADCY8, ADCY3 Adenylyl cyclase-8, brain chr12_590587_y_204 204 NINJ2 NM_016533 INTRON OMIM: 607297 NINJ2 Nerve injury-induced protein 2 chr12_78245144_r_204 204 SYT1 NM_005639 INTRON OMIM: 608081 SYT15 Synaptotagmin 15 MOUSE: 14(Syt15) chr1_173832143_y_204 204 PLAC3 NM_021936 INTRON chr1_173832143_y_204 204 PLAC3 NM_020318 INTRON chr2_25701687_r_204 204 DTNB NM_021907 INTRON OMIM: 602415 DTNB Dystrobrevin, beta MOUSE: 12(Dtnb) chr2_25701687_r_204 204 DTNB NM_033148 INTRON OMIM: 602415 DTNB Dystrobrevin, beta MOUSE: 12(Dtnb) chr2_25701687_r_204 204 DTNB NM_033147 INTRON OMIM: 602415 DTNB Dystrobrevin, beta MOUSE: 12(Dtnb) chr3_135922402_y_204 204 EPHB1 NM_004441 INTRON OMIM: 600600 EPHB1, EPHT2, NET eph tyrosine kinase 2 (ephrin receptor EphB1) chr4_110248462_r_204 204 COL25A1 NM_032518 INTRON chr6_102557679_y_204 204 GRIK2 NM_021956 INTRON OMIM: 138244 GRIK2, GLUR6 Glutamate receptor, ionotropic, kainate 2 chr6_102557679_y_204 204 GRIK2 NM_175768 UTR OMIM: 138244 GRIK2, GLUR6 Glutamate receptor, ionotropic, kainate 2 chr7_88095731_y_204 204 FLJ32110 NM_181646 INTRON chr7_91958683_r_204 204 CDK6 NM_001259 INTRON OMIM: 603368 CDK6, PLSTIRE Cyclin-dependent kinase 6 chr7_98072711_y_204 204 DKFZp761L1417 NM_152913 INTRON chr15_43674970_y_205 205 SQRDL NM_021199 INTRON chr15_88132207_y_205 205 AP3S2 NM_005829 INTRON chr1_174005095_y_205 205 PLAC3 NM_020318 INTRON chr1_44006561_y_205 205 FLJ40160 NM_173484 INTRON chr1_48254323_r_205 205 SPATA6 NM_019073 INTRON chr3_196147712_r_205 205 FLJ35155 NM_152531 INTRON chr19_6661126_r_206 206 C3 NM_000064 INTRON OMIM: 600975 GLC3B Glaucoma 3, primary infantile, B Glaucoma 3, primary infantile, B (2) chr1_97458129_y_206 206 DPYD NM_000110 INTRON OMIM: 274270 DPYD, DPD Dihydropyrimidine dehydrogenase Thymine-uraciluria (3); {Fluorouracil toxicity, sensitivity to} (3) chr5_156452275_r_206 206 HAVCR1 NM_012206 INTRON OMIM: 606518 HAVCR1, HAVCR Hepatitis A virus cellular receptor 1 chr7_99636077_y_206 206 FLJ10057 NM_017984 UTR chr8_70746983_r_206 206 SLC21A15 NM_030958 INTRON chrX_103505489_y_206 206 IL1RAPL2 NM_017416 INTRON OMIM: 300277 IL1RAPL2 Interleukin 1 receptor accessory protein-like 2 chr10_55540341_r_207 207 PCDH15 NM_033056 INTRON OMIM: 605514 PCDH15 Protocadherin 15 Usher syndrome, type 1F, 602083 (3) MOUSE: 10(av) chr11_85354457_r_207 207 MGC34732 NM_173556 INTRON chr13_99710396_y_207 207 VGCNL1 NM_052867 INTRON chr5_22290209_r_207 207 CDH12 NM_004061 UTR OMIM: 600562 CDH12, CDHB Cadherin-12 (N-cadherin 2) pseudogene on 5q13 in SMA region chr7_131664264_y_207 207 DKFZp434G0625 NM_181775 UTR chr12_9651093_y_208 208 KLRB1 NM_002258 INTRON OMIM: 602890 KLRB1, NKRP1A Killer cell lectin-like receptor, subfamily B, member 1 chr16_23844783_y_208 208 PRKCB1 NM_002738 INTRON OMIM: 176970 PRKCB1, PKCB Protein kinase C, beta 1 polypeptide chr19_16878061_y_208 208 VIP NM_015692 INTRON OMIM: 192321 VIPR1 Vasoactive intestinal peptide receptor 1 incorrectly assigned to 2q37 MOUSE: 9(Vipr1) chr1_41441428_y_208 208 HIVEP3 NM_024503 INTRON OMIM: 606649 HIVEP3, KRC Human immunodeficiency virus type 1 enhancer-binding protein 3 chr5_1149509_r_208 208 SLC12A7 NM_006598 INTRON OMIM: 604879 SLC12A7, KCC4 Solute carrier family 12 (potassium/chloride transporters), member 7 chr2_45946067_y_209 209 PRKCE NM_005400 INTRON OMIM: 176975 PRKCE, PKCE Protein kinase C, epsilon chr5_19856633_r_209 209 CDH18 NM_004934 INTRON OMIM: 608287 PCDH18, KIAA1562 Protocadherin 18 chrX_31934343_r_209 209 DMD NM_004007 INTRON OMIM: 605512 ELOVL4, ADMD, STGD2, Elongation of very long chain fatty acids 4 Stargardt disease 3, 600110 (3); Macular dystrophy, autosomaldominant, chromosom chrX_31934343_r_209 209 DMD NM_004009 INTRON OMIM: 605512 ELOVL4, ADMD, STGD2, Elongation of very long chain fatty acids 4 Stargardt disease 3, 600110 (3); Macular dystrophy, autosomaldominant, chromosom chrX_31934343_r_209 209 DMD NM_004010 INTRON OMIM: 605512 ELOVL4, ADMD, STGD2, Elongation of very long chain fatty acids 4 Stargardt disease 3, 600110 (3); Macular dystrophy, autosomaldominant, chromosom chrX_31934343_r_209 209 DMD NM_004006 INTRON OMIM: 605512 ELOVL4, ADMD, STGD2, Elongation of very long chain fatty acids 4 Stargardt disease 3, 600110 (3); Macular dystrophy, autosomaldominant, chromosom chrX_31934343_r_209 209 DMD NM_000109 INTRON OMIM: 605512 ELOVL4, ADMD, STGD2, Elongation of very long chain fatty acids 4 Stargardt disease 3, 600110 (3); Macular dystrophy, autosomaldominant, chromosom chrY_4943825_y_209 209 PCDH11Y NM_032973 INTRON OMIM: 400022 PCDH11Y, PCDH22, PCD Protocadherin 22 chr10_7612694_r_210 210 ITIH5 NM_030569 INTRON chr11_116985744_y_210 210 DSCAML1 NM_020693 INTRON chr15_61520276_y_210 210 USP3 NM_006537 INTRON OMIM: 600183 DUSP3, VHR Dual specificity phosphatase-3 (vaccinia virus phosphataseVH1-related) chr1_113279107_y_210 210 MAGI-3 NM_152900 INTRON chr1_113279107_y_210 210 MAGI-3 NM_020965 INTRON chr1_180133408_r_210 210 C1orf14 NM_030933 INTRON chr1_51343771_r_210 210 EPS15 NM_001981 INTRON OMIM: 600051 EPS15 Epidermal growth factor receptor pathway substrate-15 chr6_53217827_r_210 210 ELOVL5 NM_021814 UTR chr8_114121818_r_210 210 CSMD3 NM_052900 INTRON OMIM: 608399 CSMD3, KIAA1894 Cub and Sushi multiple domains 3 chr17_11798581_y_211 211 DNAH9 NM_001372 INTRON OMIM: 603330 DNAH9, DNAH17L, DNEL Dynein, axonemal, heavy chain 9 chr20_44629810_r_211 211 RBPSUHL NM_014276 INTRON chr2_158613250_r_211 211 ACVR1C NM_145259 INTRON chr4_2885275_y_211 211 ADD1 NM_001119 UTR OMIM: 102680 ADD1 Adducin-1, alpha {Hypertension, essential, salt-sensitive}, 145500 (3) MOUSE: 5(Add1) chr4_2885275_y_211 211 ADD1 NM_014189 UTR OMIM: 102680 ADD1 Adducin-1, alpha {Hypertension, essential, salt-sensitive}, 145500 (3) MOUSE: 5(Add1) chr4_2885275_y_211 211 ADD1 NM_014190 UTR OMIM: 102680 ADD1 Adducin-1, alpha {Hypertension, essential, salt-sensitive}, 145500 (3) MOUSE: 5(Add1) chr4_2885275_y_211 211 ADD1 NM_176801 UTR OMIM: 102680 ADD1 Adducin-1, alpha {Hypertension, essential, salt-sensitive}, 145500 (3) MOUSE: 5(Add1) chr8_68569269_y_211 211 CPA6 NM_020361 INTRON chr10_89125563_y_212 212 PAPSS2 NM_004670 INTRON chr19_6089468_r_212 212 BGR NM_030924 UTR OMIM: 300190 SH3BGR SH3-binding domain glutamic acid-rich protein-like chr2_179006640_r_212 212 PDE11A NM_016953 INTRON chr2_223774478_r_212 212 DGAT2L1 NM_058165 INTRON chr3_36400661_r_212 212 STAC NM_003149 INTRON OMIM: 602317 STAC SRC homology three (SH3) and cysteine-rich domain MOUSE: 9(Stac) chr8_117721492_r_212 212 EIF3S3 NM_003756 INTRON OMIM: 603912 EIF3S3 Eukaryotic translation initiation factor 3, subunit 3 chr12_2552196_y_213 213 CACNA1C NM_000719 INTRON OMIM: 114205 CACNA1C, CACNL1A1, C Calcium channel, voltage-dependent, L type, alpha 1C subunit chr2_166725058_r_213 213 TAIP-2 NM_024969 INTRON chr5_171464798_r_213 213 STK10 NM_005990 INTRON OMIM: 603919 STK10, LOK Serine/threonine protein kinase-10 MOUSE: 11(Stk10) chr7_14553033_r_213 213 DGKB NM_004080 INTRON OMIM: 604070 DGKB, DGK Diacylglycerol kinase, beta, 90kD chr7_14553033_r_213 213 DGKB NM_145695 INTRON OMIM: 604070 DGKB, DGK Diacylglycerol kinase, beta, 90kD chrX_102778341_y_213 213 IL1RAPL2 NM_017416 INTRON OMIM: 300277 IL1RAPL2 Interleukin 1 receptor accessory protein-like 2 chr12_43870057_y_214 214 LOC51054 NM_015899 UTR chr13_93546811_r_214 214 ABCC4 NM_005845 INTRON OMIM: 605250 ABCC4, MRP4, MOATB ATP-binding cassette, subfamily C, member 4 chr15_67053620_y_214 214 NOX5 NM_024505 INTRON OMIM: 606572 NOX5, NOX5A, NOX5B NADPH oxidase 5 chr1_214141940_r_214 214 ESRRG NM_001438 UTR OMIM: 602969 ESRRG Estrogen-related receptor, gamma chr7_70557073_y_214 214 WBSCR17 NM_022479 INTRON chr8_99060625_y_214 214 FLJ39553 NM_173549 INTRON chr9_97092539_y_214 214 COL15A1 NM_001855 INTRON OMIM: 120325 COL15A1 Collagen XV, alpha-1 polypeptide MOUSE: 4(Col15a1) chr17_64770790_r_215 215 APOH NM_000042 INTRON OMIM: 138700 APOH Apolipoprotein H (beta-2-glycoprotein I) [Apolipoprotein H deficiency] (3) MOUSE: 11(Apoh) chr19_59673405_r_215 215 CDC42EP5 NM_145057 UTR chr1_180482227_y_215 215 NMNAT2 NM_015039 INTRON chr1_180482227_y_215 215 NMNAT2 NM_170706 INTRON chr2_193031492_y_215 215 TMEFF2 NM_016192 INTRON OMIM: 605734 TMEFF2, HPP1, TR Transmembrane protein with EGF-like and 2 follistatin-like domains 2 chr6_38056259_y_215 215 TEX27 NM_021943 INTRON chr15_25844494_r_216 216 OCA2 NM_000275 INTRON OMIM: 120436 MLH1, COCA2, HNPCC2 mutL, E. coli, homolog of, 1 Colorectal cancer, hereditary nonpolyposis, type 2, 114500 (3);Turcot syndrome w chr18_19301241_y_216 216 RIOK3 NM_003831 INTRON chr18_19301241_y_216 216 RIOK3 NM_145906 INTRON chr3_144804712_y_216 216 FLJ35613 NM_173653 INTRON chr3_197864584_y_216 216 PAK2 NM_002577 INTRON chr6_125473773_y_216 216 TPD52L1 NM_003287 INTRON chr9_110307900_r_216 216 DKFZP761E1824 NM_022486 UTR chrX_84694106_r_216 216 DACH2 NM_053281 INTRON chr10_120711302_r_217 217 GPRK5 NM_005308 INTRON OMIM: 600870 GPRK5, GRK5 G protein-coupled receptor kinase-5 chr14_70509682_y_217 217 RGS6 NM_004296 INTRON OMIM: 603894 RGS6 Regulator of G protein signaling 6 chr1_154771795_y_217 217 IRTA1 NM_031282 INTRON OMIM: 605876 IRTA1 Immunoglobulin superfamily receptor translocation-associated gene 1 fused with IGHA1 in multiple myeloma chr2_45918192_r_217 217 PRKCE NM_005400 INTRON OMIM: 176975 PRKCE, PKCE Protein kinase C, epsilon chr6_168228305_r_217 217 FRMD1 NM_024919 INTRON chr7_90427439_y_217 217 PFTK1 NM_012395 UTR chr8_19467182_r_217 217 ChGn NM_018371 UTR chr8_74964134_y_217 217 LY96 NM_015364 INTRON chr9_81551654_r_217 217 MGC20553 NM_174938 INTRON chrX_75567537_r_217 217 ATRX NM_000489 INTRON OMIM: 300032 ATRX, XH2, XNP, MRXS ATR-X gene (helicase 2; X-linked nuclear protein) Alpha-thalassemia/mental retardation syndrome, 301040 (3);Juberg-Marsidi syndrom MOUSE: X(Xh2) chrX_75567537_r_217 217 ATRX NM_138270 INTRON OMIM: 300032 ATRX, XH2, XNP, MRXS ATR-X gene (helicase 2; X-linked nuclear protein) Alpha-thalassemia/mental retardation syndrome, 301040 (3);Juberg-Marsidi syndrom MOUSE: X(Xh2) chrX_75567537_r_217 217 ATRX NM_138271 INTRON OMIM: 300032 ATRX, XH2, XNP, MRXS ATR-X gene (helicase 2; X-linked nuclear protein) Alpha-thalassemia/mental retardation syndrome, 301040 (3);Juberg-Marsidi syndrom MOUSE: X(Xh2) chr2_116237115_r_218 218 DPP10 NM_020868 INTRON chr6_76077913_r_218 218 FILIP1 NM_015687 INTRON chr7_131664956_y_218 218 DKFZp434G0625 NM_181775 UTR chr10_130836861_y_219 219 MGMT NM_002412 INTRON OMIM: 156569 MGMT Methylguanine-DNA methyltransferase chr14_54103151_y_219 219 KTN1 NM_004986 INTRON OMIM: 600381 KTN1, CG1 Kinectin chr17_32212354_r_219 219 ACCN1 NM_001094 INTRON OMIM: 601784 ACCN1, BNC1, MDEG Amiloride-sensitive cation channel 1, neuronal (degenerin) chr5_37542828_y_219 219 FLJ10233 NM_018034 INTRON chrX_3150125_r_219 219 PRKX NM_005044 INTRON OMIM: 300083 PRKX Protein kinase, X-linked chr13_26845782_r_220 220 FLT1 NM_002019 INTRON OMIM: 165070 FLT1 fms-related tyrosine kinase-1 (vascular endothelial growthfactor/vascular permea 150kb from FLT3 chr15_54948696_y_220 220 TCF12 NM_003205 INTRON OMIM: 600480 TCF12, HTF4 Transcription factor-12 (HTF4, helix-loop-helix transcriptionfactors-4) chr1_193950043_y_220 220 HF1 NM_000186 INTRON OMIM: 134370 HF1, CFH, HUS H factor-1 (complement factor H) Factor H deficiency (1); Membroproliferative glomerulonephritis (1);Hemolytic-ur MOUSE: 1(Cfh) chr1_58353775_r_220 220 MPRP-1 NM_145243 INTRON chr5_108310392_y_220 220 FER NM_005246 INTRON OMIM: 176942 FER, TYK3 fer (fps/fes related) tyrosine kinase MOUSE: 11(Fert) chr11_124900883_r_221 221 FEZ1 NM_005103 UTR OMIM: 606551 LZTS1, F37, FEZ1 Leucine zipper, putative tumor suppressor 1 Esophageal squamous cell carcinoma, 133239 (3) chr11_124900883_r_221 221 FEZ1 NM_022549 UTR OMIM: 606551 LZTS1, F37, FEZ1 Leucine zipper, putative tumor suppressor 1 Esophageal squamous cell carcinoma, 133239 (3) chr18_2604435_r_221 221 HEC NM_006101 INTRON chr1_27748115_r_221 221 STX12 NM_177424 INTRON chr3_101563374_y_221 221 FLJ10134 NM_018004 UTR chr3_4627541_y_221 221 ITPR1 NM_002222 INTRON OMIM: 147265 ITPR1 Inositol 1,4,5-triphosphate receptor, type 1 MOUSE: 6(Itpr1) chr12_100375383_r_222 222 SPIC NM_152323 INTRON chr12_90003422_r_222 222 LUM NM_002345 INTRON OMIM: 600616 LUM, LDC Lumican MOUSE: 10(Ldc) chr1_229077709_y_222 222 DISC1 NM_018662 INTRON OMIM: 605210 DISC1 Disrupted in schizophrenia 1 Schizophrenia, 181500 (2) MOUSE: 8(Disc1) chr20_45914310_r_222 222 SLC13A3 NM_022829 INTRON OMIM: 606411 SLC13A3, NADC3 Solute carrier family 13 (sodium-dependent dicarboxylate transporter),member 3 chr3_89204710_y_222 222 EPHA3 NM_005233 INTRON OMIM: 179611 EPHA3, ETK1, HEK Ephrin receptor EphA3 (human embryo kinase 1) chr3_89204710_y_222 222 EPHA3 NM_182644 INTRON OMIM: 179611 EPHA3, ETK1, HEK Ephrin receptor EphA3 (human embryo kinase 1) chr7_131663007_y_222 222 DKFZp434G0625 NM_181775 UTR chr10_12669323_y_223 223 CKLiK NM_153498 INTRON chr10_12669323_y_223 223 CKLiK NM_020397 INTRON chr15_65329569_y_223 223 FLJ12476 NM_022784 UTR chr18_58985449_y_223 223 BCL2 NM_000633 INTRON OMIM: 603827 BCL2L11, BIM BCL2-like 11 ?2p13 chr1_158251331_r_223 223 LOC257106 NM_181720 INTRON chr1_57530817_r_223 223 DAB1 NM_021080 UTR OMIM: 603448 DAB1 Disabled, Drosophila, homolog 1 MOUSE: 4(Dab1) chr9_126359209_y_223 223 DNM1 NM_004408 INTRON OMIM: 602377 DNM1 Dynamin-1 MOUSE: 2(Dnm1) chr12_12990452_y_224 224 GPRC5D NM_018654 INTRON OMIM: 607437 GPRC5D G protein-coupled receptor, family C, group 5, member D chr14_71213572_r_224 224 DPF3 NM_012074 INTRON chr1_238197527_r_224 224 RGS7 NM_002924 INTRON chr1_30947573_r_224 224 PUM1 NM_014676 INTRON OMIM: 607204 PUM1, KIAA0099 Pumilio, Drosophila, homolog of, 1 chr22_37597579_y_224 224 APOBEC3A NM_145699 INTRON OMIM: 607109 APOBEC3A, PHRBN Apolipoprotein B mRNA editing enzyme, catalytic polypeptide-like 3A(phorbolin 1) chr3_172803514_r_224 224 PLD1 NM_002662 UTR OMIM: 602382 PLD1 Phospholipase D1, phosphatidylcholine-specific MOUSE: 3(Pld1) chr9_27434113_r_224 224 FLJ13204 NM_024761 INTRON chrX_102599023_y_224 224 IL1RAPL2 NM_017416 UTR OMIM: 300277 IL1RAPL2 Interleukin 1 receptor accessory protein-like 2 chr12_24880977_r_225 225 BCAT1 NM_005504 INTRON OMIM: 113520 BCAT1, BCT1 Branched chain aminotransferase-1, cytosolic ?Hyperleucinemia-isoleucinemia or hypervalinemia (1) MOUSE: 6(Bcat1) chr13_72329057_r_225 225 KLF12 NM_007249 INTRON OMIM: 607531 KLF12, AP2REP Kruppel-like factor 12 chr13_72329057_r_225 225 KLF12 NM_016285 INTRON OMIM: 607531 KLF12, AP2REP Kruppel-like factor 12 chr6_125562574_r_225 225 TPD52L1 NM_003287 INTRON chr7_131689619_r_225 225 DKFZp434G0625 NM_181775 UTR chr16_23321331_r_226 226 SCNN1B NM_000336 UTR OMIM: 600760 SCNN1B Sodium channel, nonvoltage-gated 1, beta Liddle syndrome, 177200 (3); Pseudohypoaldosteronism, type I, 264350(3) MOUSE: 7(Scnn1b) chr19_2590924_r_226 226 FLJ00058 NM_052847 UTR chr19_38940125_r_227 227 CHST8 NM_022467 INTRON chr1_66671725_r_227 227 FLJ23129 NM_024763 UTR chr2_158885729_r_227 227 ACVR1 NM_001105 UTR OMIM: 102576 ACVR1, ACVRLK2, ALK2 Activin A receptor, type I chr4_21509602_r_227 227 KCNIP4 NM_147182 UTR OMIM: 608182 KCNIP4, KCHIP4 Kv channel-interacting protein 4 chr2_125559701_r_228 228 caspr5 NM_130773 INTRON chr2_125559701_r_228 228 caspr5 NM_138996 INTRON chr7_136549324_r_228 228 DGKI NM_004717 INTRON OMIM: 604072 DGKI Diacylglycerol kinase, iota, 130-kD chr1_172539511_y_229 229 TNR NM_003285 INTRON OMIM: 601995 TNR Tenascin R (restrictin, janusin) MOUSE: 4(Tnr) chr2_74762717_r_229 229 LOC130951 NM_138804 INTRON chr3_191004670_r_229 229 MLAT4 NM_018192 INTRON chr3_193762620_r_229 229 FGF12 NM_004113 INTRON OMIM: 601513 FGF12, FHF1 Fibroblast growth factor-12 MOUSE: 16(Fhf1) chr3_78854590_r_229 229 ROBO1 NM_133631 INTRON OMIM: 602430 ROBO1, DUTT1, SAX3 Roudnabout, Drosophila, homolog of, 1 chr3_78854590_r_229 229 ROBO1 NM_002941 INTRON OMIM: 602430 ROBO1, DUTT1, SAX3 Roudnabout, Drosophila, homolog of, 1 chr7_107177881_y_229 229 LAMB1 NM_002291 INTRON OMIM: 150240 LAMB1 Laminin, beta-1 ?7q22 ?Cutis laxa, marfanoid neonatal type (1) MOUSE: 1(Lamb1) chr14_50487228_r_230 230 NID2 NM_007361 INTRON OMIM: 605399 NID2 Nidogen 2 MOUSE: 14(Nid2) chr14_50487228_r_230 230 CGI-99 NM_016039 UTR chr1_211720670_r_230 230 PTPN14 NM_005401 UTR OMIM: 603155 PTPN14, PEZ Protein tyrosine phosphatase, nonreceptor-type, 14 chr21_31796147_r_230 230 TIAM1 NM_003253 UTR OMIM: 600687 TIAM1 T-cell lymphoma invasion and metastasis 1 MOUSE: 16(Tiam1) chr22_31145110_y_230 230 BPIL2 NM_174932 INTRON chr2_27129410_r_230 230 DPYSL5 NM_020134 INTRON OMIM: 608383 DPYSL5, CRMP5, CRAM Dihydropyrimidinase-like 5 MOUSE: 5(Dpysl5) chr5_9405885_r_230 230 SEMA5A NM_003966 INTRON chr6_116325361_r_230 230 FRK NM_002031 INTRON OMIM: 606573 FRK, RAK, GTK FYN-related kinase chr8_106502893_y_230 230 ZFPM2 NM_012082 INTRON OMIM: 603693 ZFPM2, FOG2 Zinc finger protein, multitype 2 (friend of GATA2) chr1_18118862_r_231 231 MGC15730 NM_032880 INTRON chr1_65722707_y_231 231 PDE4B NM_002600 UTR OMIM: 600127 PDE4B, DPDE4 Phosphodiesterase-4B, cAMP-specific (dunce-like phosphodiesterase E4) MOUSE: 4(Pde4b) chr2_125559469_r_231 231 caspr5 NM_130773 INTRON chr2_125559469_r_231 231 caspr5 NM_138996 INTRON chr4_185748184_y_231 231 MGC33971 NM_153343 INTRON chrX_30042217_y_231 231 GK NM_000167 INTRON OMIM: 605087 PIGK, GPI8 Phosphatidylinositol glycan, class K chr14_71471978_r_232 232 ZFYVE1 NM_021260 INTRON chr6_38888620_y_232 232 DNAH8 NM_001371 INTRON chr7_43471628_r_232 232 FLJ10803 NM_018224 UTR chr7_726247_r_232 232 CENTA1 NM_006869 INTRON chr10_120715994_y_233 233 GPRK5 NM_005308 INTRON OMIM: 600870 GPRK5, GRK5 G protein-coupled receptor kinase-5 chr12_2551932_y_233 233 CACNA1C NM_000719 INTRON OMIM: 114205 CACNA1C, CACNL1A1, C Calcium channel, voltage-dependent, L type, alpha 1C subunit chr17_73328140_r_233 233 RAB37 NM_175738 INTRON chr2_183583908_r_233 233 PDE1A NM_005019 INTRON OMIM: 171890 PDE1A Phosphodiesterase-1A chr10_77467475_r_234 234 CDA017 NM_032024 INTRON chr12_70636441_y_234 234 TPH2 NM_173353 INTRON OMIM: 191070 TDO2, TPH2, TRPO Tryptophan oxygenase chr5_21924362_r_234 234 CDH12 NM_004061 INTRON OMIM: 600562 CDH12, CDHB Cadherin-12 (N-cadherin 2) pseudogene on 5q13 in SMA region chr13_40579109_y_235 235 DGKH NM_152910 INTRON chr13_40579109_y_235 235 DGKH NM_178009 INTRON chr16_83313511_y_235 235 CDH13 NM_001257 INTRON OMIM: 601364 CDH13, CDHH Cadherin-13 (H-cadherin, heart) chr5_158259292_r_235 235 EBF NM_024007 INTRON OMIM: 164343 EBF, OLF1 Early B-cell factor (olfactory neuronal transcription factor 1) MOUSE: 11(Ebf) chr7_70983792_r_235 235 CALN1 NM_031468 INTRON chrX_8065022_r_235 235 KAL1 NM_000216 INTRON OMIM: 308700 KAL1, KMS, ADMLX Kallmann syndrome-1 sequence (anosmin-1) with ichthyosis in probable microdeletion syndrome Kallmann syndrome (3) chr13_47690589_r_236 236 FLJ12577 NM_030925 INTRON chr19_6380344_r_236 236 MGC34725 NM_173637 INTRON chr18_42542274_y_237 237 SIAT8E NM_013305 INTRON OMIM: 607162 SIAT8E Sialyltransferase 8E chr22_24418578_r_237 237 ADRBK2 NM_005160 INTRON OMIM: 109636 ADRBK2, BARK2 Adrenergic, beta, receptor kinase-2 chr4_185774444_y_237 237 MGC33971 NM_153343 INTRON chr7_139058886_r_237 237 TBXAS1 NM_001061 INTRON OMIM: 274180 TBXAS1 Thromboxane A synthase 1, platelet Thromboxane synthase deficiency (2) MOUSE: 6(Tbxas1) chr7_139058886_r_237 237 TBXAS1 NM_030984 INTRON OMIM: 274180 TBXAS1 Thromboxane A synthase 1, platelet Thromboxane synthase deficiency (2) MOUSE: 6(Tbxas1) chr17_64398471_y_238 238 MGC33887 NM_145036 INTRON chr18_45357358_r_238 238 LIPG NM_006033 INTRON chr2_228108944_r_238 238 COL4A4 NM_000092 INTRON OMIM: 120131 COL4A4 Collagen IV, alpha-4 polypeptide head-to-head with COL4A4 in same YAC Alport syndrome, autosomal recessive, 203780 (3); Hematuria,familial benign (3) chr10_72507659_y_239 239 CDH23 NM_052836 UTR OMIM: 605516 CDH23, USH1D Cadherin-23 (otocadherin) between D10S529 and D10S573 Usher syndrome, type 1D, 601067 (3); Deafness, autosomal recessive12, 601386 (3) MOUSE: 10(Cdh23, v) chr10_72507659_y_239 239 CDH23 NM_022124 UTR OMIM: 605516 CDH23, USH1D Cadherin-23 (otocadherin) between D10S529 and D10S573 Usher syndrome, type 1D, 601067 (3); Deafness, autosomal recessive12, 601386 (3) MOUSE: 10(Cdh23, v) chr12_7144801_y_239 239 LOC51279 NM_016546 INTRON chr5_115570194_y_239 239 PTD002 NM_016144 INTRON chr8_68122016_y_239 239 FLJ22490 NM_024790 UTR chr12_22365024_r_240 240 SIAT8A NM_003034 INTRON chr1_233610154_y_240 240 EDARADD NM_145861 INTRON OMIM: 606603 EDARADD EDAR-associated death domain MOUSE: 13(Edaradd) chr1_233610154_y_240 240 EDARADD NM_080738 INTRON OMIM: 606603 EDARADD EDAR-associated death domain MOUSE: 13(Edaradd) chr1_46635698_y_240 240 CYP4B1 NM_000779 INTRON OMIM: 124075 CYP4B1 Cytochrome P450, subfamily IVB, polypeptide 1 MOUSE: 4(Cyp4a) chr20_31357841_y_240 240 C20orf160 NM_080625 INTRON chr12_8094677_y_241 241 FHX NM_018416 INTRON OMIM: 605802 ZFHX1B, SMADIP1, SIP SMAD-interacting protein 1 (zinc finger homeobox 1B) Mowat-Wilson syndrome, 235730 (3) chr22_34109736_y_241 241 HMOX1 NM_002133 INTRON OMIM: 141250 HMOX1 Heme oxygenase, decycling, 1 Heme oxygenase-1 deficiency (3) chr4_104088791_r_241 241 MANBA NM_005908 INTRON OMIM: 248510 MANBA, MANB1 Mannosidase, beta A, lysosomal linked in mouse to Adl-3 Mannosidosis, beta- (3) MOUSE: 3(Bmn) chr4_56400366_y_241 241 NMU NM_006681 INTRON chr11_60492167_r_242 242 PHT2 NM_016582 INTRON OMIM: 600600 EPHB1, EPHT2, NET eph tyrosine kinase 2 (ephrin receptor EphB1) chr6_54222248_y_242 242 TINAG NM_014464 INTRON OMIM: 606749 TINAG, TIN1, TIN2 Tubulointerstitial nephritis antigen chr6_83942534_r_242 242 ME1 NM_002395 INTRON OMIM: 154250 ME1 Malic enzyme, cytoplasmic MOUSE: 9(Mod1) chr9_117388240_r_242 242 DBCCR1 NM_014618 INTRON OMIM: 602865 DBCCR1 Deleted in bladder cancer chromosome region candidate 1 chr7_100679190_y_243 243 COL26A1 NM_133457 INTRON chr7_27892315_r_243 243 JAZF1 NM_175061 INTRON OMIM: 606246 JAZF1 JAZF1 gene Endometrial stromal tumors (2) chr6_124680820_r_244 244 TCBA1 NM_153355 INTRON chr2_222634031_r_245 245 EPHA4 NM_004438 INTRON chr3_85538434_y_245 245 LOC253559 NM_153184 INTRON chr7_131799651_r_245 245 FLJ40288 NM_173682 UTR chrX_14813534_r_245 245 PIR NM_003662 INTRON OMIM: 603092 DUSP11, PIR1 Dual specificity phosphatase-11, RNA/RNP complex-interacting chr12_94804686_r_246 246 FLJ40089 NM_182496 INTRON chr18_75506189_r_246 246 FLJ25715 NM_182570 INTRON chr19_2647153_r_246 246 FLJ00058 NM_052847 UTR chr17_67174613_y_247 247 DKFZp434F2322 NM_017565 INTRON chr19_59364304_y_247 247 TMC4 NM_144686 INTRON chr1_97068016_y_247 247 DPYD NM_000110 INTRON OMIM: 274270 DPYD, DPD Dihydropyrimidine dehydrogenase Thymine-uraciluria (3); {Fluorouracil toxicity, sensitivity to} (3) chr6_117166909_y_247 247 GPRC6A NM_148963 INTRON chrX_14747500_r_247 247 FIGF NM_004469 INTRON OMIM: 300091 FIGF, VEGFD c-fos induced growth factor (vascular endothelial growth factor D) chr10_22010455_y_248 248 MLLT10 NM_004641 INTRON chr3_78681306_y_248 248 ROBO1 NM_133631 INTRON OMIM: 602430 ROBO1, DUTT1, SAX3 Roudnabout, Drosophila, homolog of, 1 chr3_78681306_y_248 248 ROBO1 NM_002941 INTRON OMIM: 602430 ROBO1, DUTT1, SAX3 Roudnabout, Drosophila, homolog of, 1 chr13_98698974_y_249 249 PCCA NM_000282 INTRON OMIM: 232000 PCCA Propionyl Coenzyme A carboxylase, alpha polypeptide Propionicacidemia, 606054 (3) MOUSE: 14(Pcca) chr14_40240730_r_250 250 C14orf146 NM_152447 UTR chr4_30808871_r_250 250 PCDH7 NM_032457 INTRON OMIM: 602988 PCDH7, BHPCDH Protocadherin-7 chr7_100667143_y_250 250 COL26A1 NM_133457 INTRON chrX_106541625_y_250 250 COL4A5 NM_000495 INTRON OMIM: 303630 COL4A5, ATS, ASLN Collagen IV, alpha-5 polypeptide diffuse leiomyomatosis with Alport syndrome = contiguous genesyndrome with COL4A Alport syndrome, 301050 (3) MOUSE: X(Col4a5) chrX_106541625_y_250 250 COL4A5 NM_033380 INTRON OMIM: 303630 COL4A5, ATS, ASLN Collagen IV, alpha-5 polypeptide diffuse leiomyomatosis with Alport syndrome = contiguous genesyndrome with COL4A Alport syndrome, 301050 (3) MOUSE: X(Col4a5) chrX_106541625_y_250 250 COL4A5 NM_033381 INTRON OMIM: 303630 COL4A5, ATS, ASLN Collagen IV, alpha-5 polypeptide diffuse leiomyomatosis with Alport syndrome = contiguous genesyndrome with COL4A Alport syndrome, 301050 (3) MOUSE: X(Col4a5) chrX_75648210_r_250 250 ATRX NM_000489 INTRON OMIM: 300032 ATRX, XH2, XNP, MRXS ATR-X gene (helicase 2; X-linked nuclear protein) Alpha-thalassemia/mental retardation syndrome, 301040 (3);Juberg-Marsidi syndrom MOUSE: X(Xh2) chrX_75648210_r_250 250 ATRX NM_138270 INTRON OMIM: 300032 ATRX, XH2, XNP, MRXS ATR-X gene (helicase 2; X-linked nuclear protein) Alpha-thalassemia/mental retardation syndrome, 301040 (3);Juberg-Marsidi syndrom MOUSE: X(Xh2) chrX_75648210_r_250 250 ATRX NM_138271 INTRON OMIM: 300032 ATRX, XH2, XNP, MRXS ATR-X gene (helicase 2; X-linked nuclear protein) Alpha-thalassemia/mental retardation syndrome, 301040 (3);Juberg-Marsidi syndrom MOUSE: X(Xh2) chr3_158310932_y_251 251 FLJ12604 NM_024621 INTRON chr5_178871747_r_251 251 ADAMTS2 NM_014244 INTRON OMIM: 604539 ADAMTS2, NPI A disintegrin-like and metalloproteinase with thrombospondin type 1motif, 2 (pro Ehlers-Danlos syndrome, type VIIC, 225410 (3) MOUSE: 11(Adamts2) chr5_178871747_r_251 251 ADAMTS2 NM_021599 INTRON OMIM: 604539 ADAMTS2, NPI A disintegrin-like and metalloproteinase with thrombospondin type 1motif, 2 (pro Ehlers-Danlos syndrome, type VIIC, 225410 (3) MOUSE: 11(Adamts2) chr3_123373256_r_252 252 CSTA NM_005213 INTRON OMIM: 184600 CSTA, STFA, STF1 Cystatin A (stefin A) MOUSE: 16(Stf1) chr6_100906010_r_252 252 SIM1 NM_005068 INTRON OMIM: 603128 SIM1 Single-minded, Drosophila, homolog of, 1 Obesity, severe, 601665 (3) MOUSE: 10(Sim1) chr7_115749997_r_252 252 CAV1 NM_001753 INTRON OMIM: 601047 CAV1 Caveolin-1 chr5_151257166_y_253 253 GLRA1 NM_000171 INTRON OMIM: 138491 GLRA1, STHE Glycine receptor, alpha-1 polypeptide Startle disease/hyperekplexia, autosomal dominant, 149400 (3);Startle disease, a MOUSE: 11(spd) chr19_4118333_r_254 254 CREB-H NM_032607 INTRON chr19_4118333_r_254 254 FLJ10374 NM_018074 UTR chr1_66495617_r_254 254 DKFZp761D221 NM_032291 INTRON chr20_42382016_r_254 254 PTPRT NM_007050 INTRON chr20_42382016_r_254 254 PTPRT NM_133170 INTRON chr7_131664587_y_254 254 DKFZp434G0625 NM_181775 UTR chr14_35499439_r_255 255 SLC25A21 NM_030631 INTRON OMIM: 607571 SLC25A21, ODC Solute carrier family 25 (mitochondrial oxodicarbosylate carrier),member 21 chr12_102912877_r_256 256 LOC83468 NM_031302 INTRON chrX_146401633_y_256 256 FMR2 NM_002025 INTRON OMIM: 309548 FMR2, FRAXE, MRX2 Fragile site, X-linked, E Mental retardation, X-linked, FRAXE type (3) chr2_80244630_y_257 257 CTNNA2 NM_004389 INTRON OMIM: 114025 CTNNA2, CAPR, CTNR Catenin, alpha-2 (cadherin-associated protein, related) MOUSE: 6(Capr) chr18_6061633_r_258 258 FLJ35936 NM_173464 INTRON chr19_8545400_y_258 258 MYO1F NM_012335 INTRON OMIM: 601480 MYO1F Myosin IF MOUSE: 17(Myo1f) chr19_14607796_y_259 259 EMR3 NM_032571 INTRON chr19_14607796_y_259 259 EMR3 NM_152939 UTR chr8_87113913_r_259 259 ATP6V0D2 NM_152565 INTRON chr12_118305562_r_260 260 MGC39827 NM_178499 INTRON chr10_12873208_y_261 261 CKLiK NM_153498 INTRON chr7_104371761_r_261 261 SRPK2 NM_003138 INTRON chr7_104371761_r_261 261 SRPK2 NM_182691 INTRON chr7_104371761_r_261 261 SRPK2 NM_182692 INTRON chr8_68437883_y_261 261 CPA6 NM_020361 INTRON chr16_24243139_r_262 262 CACNG3 NM_006539 INTRON OMIM: 606403 CACNG3 Calcium channel, voltage-dependent, gamma-3 subunit chr20_45495637_y_262 262 CDH22 NM_021248 INTRON OMIM: 400022 PCDH11Y, PCDH22, PCD Protocadherin 22 chr1_189898521_r_263 263 RGS13 NM_002927 UTR chr1_189898521_r_263 263 RGS13 NM_144766 UTR chr2_119839239_r_263 263 MARCO NM_006770 INTRON chr4_77505162_r_264 264 NUP54 NM_017426 INTRON OMIM: 607607 NUP54 Nucleoporin, 54kD chr8_98962841_r_265 265 MATN2 NM_002380 INTRON OMIM: 602108 MATN2 Matrilin 2 chr8_98962841_r_265 265 MATN2 NM_030583 INTRON OMIM: 602108 MATN2 Matrilin 2 chr17_8211695_r_266 266 ALOXE3 NM_021628 INTRON OMIM: 607206 ALOXE3 Arachidonate lipoxygenase 3 Ichthyosiform erythroderma, congenital, nonbullous, 1, 242100 (3) chr3_29881262_r_266 266 RBMS3 NM_014483 INTRON OMIM: 605786 RBMS3 RNA-binding motif protein, single strand-interacting, 3 chr10_78045322_r_267 267 KCNMA1 NM_002247 INTRON OMIM: 600150 KCNMA1, SLO Potassium large conductance calcium-activated channel, subfamily M,alpha member chr16_78418079_y_267 267 WWOX NM_018560 INTRON OMIM: 605131 WWOX, FOR WW domain-containing oxidoreductase Esophageal squamous cell carcinoma, 133239 (3) MOUSE: 8(Wox1, Fra8E1) chr16_78418079_y_267 267 WWOX NM_016373 INTRON OMIM: 605131 WWOX, FOR WW domain-containing oxidoreductase Esophageal squamous cell carcinoma, 133239 (3) MOUSE: 8(Wox1, Fra8E1) chr16_78418079_y_267 267 WWOX NM_130788 INTRON OMIM: 605131 WWOX, FOR WW domain-containing oxidoreductase Esophageal squamous cell carcinoma, 133239 (3) MOUSE: 8(Wox1, Fra8E1) chr16_78418079_y_267 267 WWOX NM_130790 INTRON OMIM: 605131 WWOX, FOR WW domain-containing oxidoreductase Esophageal squamous cell carcinoma, 133239 (3) MOUSE: 8(Wox1, Fra8E1) chr16_78418079_y_267 267 WWOX NM_130792 INTRON OMIM: 605131 WWOX, FOR WW domain-containing oxidoreductase Esophageal squamous cell carcinoma, 133239 (3) MOUSE: 8(Wox1, Fra8E1) chr20_45537666_y_267 267 CDH22 NM_021248 INTRON OMIM: 400022 PCDH11Y, PCDH22, PCD Protocadherin 22 chr11_991419_y_268 268 AP2A2 NM_012305 INTRON chr2_166725965_r_268 268 TAIP-2 NM_024969 INTRON chr5_63994938_r_268 268 FLJ36754 NM_173829 UTR chrX_9202531_y_268 268 APXL NM_001649 INTRON OMIM: 300103 APXL Apical protein, Xenopus laevis-like MOUSE: X(Apxl) chr19_62340999_r_269 269 ZIM3 NM_052882 INTRON chr22_25347809_y_270 270 CRYBA4 NM_001886 INTRON OMIM: 123631 CRYBA4 Crystallin, beta polypeptide A4 chr4_40899745_r_270 270 APBB2 NM_173075 UTR OMIM: 602710 APBB2, FE65L1 Amyloid beta A4 precursor protein-binding, family B, member 2(Fe65-like 1) chrX_66509113_r_270 270 OPHN1 NM_002547 INTRON OMIM: 300127 OPHN1 Oligophrenin-1 Mental retardation, X-linked, 60 (3) chr19_53583752_r_272 272 KDELR1 NM_006801 INTRON chr12_18347283_y_273 273 PIK3C2G NM_004570 INTRON chr3_72401337_r_273 273 RYBP NM_012234 INTRON OMIM: 607535 RYBP, YEAF1 Ring1- and YY1-binding protein chr7_146314566_r_273 273 CNTNAP2 NM_014141 INTRON OMIM: 604569 CNTNAP2, CASPR2, NRX Contactin-associated protein-like 2 chr3_173999568_y_274 274 NYD-SP12 NM_031955 INTRON chr17_32571716_r_275 275 ACCN1 NM_001094 INTRON OMIM: 601784 ACCN1, BNC1, MDEG Amiloride-sensitive cation channel 1, neuronal (degenerin) chr3_197263586_r_276 276 ZDHHC19 NM_144637 INTRON chr8_108338946_r_276 276 ANGPT1 NM_001146 INTRON OMIM: 601667 ANGPT1, ANG1 Angiopoietin-1 MOUSE: 15(Angpt1) chr8_108338946_r_276 276 ANGPT1 NM_139290 INTRON OMIM: 601667 ANGPT1, ANG1 Angiopoietin-1 MOUSE: 15(Angpt1) chr16_58220703_r_277 277 CSNK2A2 NM_001896 UTR OMIM: 115442 CSNK2A2 Casein kinase-2, alpha-prime polypeptide MOUSE: 8(Csnk2a2) chr18_48864310_y_277 277 DCC NM_005215 INTRON OMIM: 608378 SDCCAG1 Serologically defined colon cancer antigen 1 chr1_238811993_r_277 277 OPN3 NM_014322 INTRON OMIM: 606695 OPN3, ECPN Opsin 3 chr4_186269885_r_278 278 FLJ33167 NM_152683 UTR chr6_72697686_y_278 278 RIMS1 NM_014989 INTRON OMIM: 606629 RIMS1, RIM1, RIM, KI Regulating synaptic membrane exocytosis 1 chr2_99864171_y_279 279 LAF4 NM_002285 INTRON OMIM: 601464 LAF4 Lymphoid nuclear protein related to AF4 MOUSE: 1(Laf4) chr6_20276764_r_279 279 MGC44669 NM_175879 INTRON chr7_48195368_y_279 279 ABCA13 NM_152701 INTRON chrX_66373690_r_279 279 OPHN1 NM_002547 INTRON OMIM: 300127 OPHN1 Oligophrenin-1 Mental retardation, X-linked, 60 (3) chr17_71493219_r_280 280 C17orf26 NM_139177 INTRON chr2_125639008_r_280 280 caspr5 NM_130773 INTRON chr2_125639008_r_280 280 caspr5 NM_138996 INTRON chr1_151944729_r_281 281 KCNN3 NM_170782 INTRON OMIM: 602983 KCNN3, SK3, SKCA3 Potassium channel, calcium-activated, intermediate/small conductance,subfamily N chr1_151944729_r_281 281 KCNN3 NM_002249 INTRON OMIM: 602983 KCNN3, SK3, SKCA3 Potassium channel, calcium-activated, intermediate/small conductance,subfamily N chr2_235123103_y_281 281 TRPM8 NM_024080 INTRON OMIM: 606678 TRPM8, TRPP8 Transient receptor potential cation channel, subfamily M, member 8 chr5_31348316_r_281 281 CDH6 NM_004932 INTRON OMIM: 603007 CDH6 Cadherin 6 chrX_63015297_y_281 281 HCA127 NM_018684 INTRON chr10_23624112_r_282 282 MGC46732 NM_153714 INTRON chr11_16118081_r_283 283 SOX6 NM_033326 INTRON OMIM: 607257 SOX6 SRY-box 6 MOUSE: 7(Sox6) chr1_23840354_y_283 283 IL28RA NM_170743 INTRON OMIM: 607404 IL28RA Interleukin 28 receptor, alpha chr1_23840354_y_283 283 IL28RA NM_173064 INTRON OMIM: 607404 IL28RA Interleukin 28 receptor, alpha chr1_23840354_y_283 283 IL28RA NM_173065 INTRON OMIM: 607404 IL28RA Interleukin 28 receptor, alpha chr7_70557500_y_283 283 WBSCR17 NM_022479 INTRON chr11_117505154_r_284 284 SCN2B NM_004588 UTR OMIM: 601327 SCN2B Sodium channel, voltage-gated, type II, beta polypeptide MOUSE: 9(Scn2b) chr11_117505154_r_284 284 TMPRSS4 NM_019894 INTRON OMIM: 606565 TMPRSS4 Transmembrane protease, serine 4 chr2_175521891_r_284 284 FLJ31819 NM_152529 INTRON chr3_37514072_y_284 284 ITGA9 NM_002207 INTRON OMIM: 603963 ITGA9 Integrin, alpha-9 chr18_61598108_y_286 286 CDH7 NM_033646 INTRON OMIM: 602988 PCDH7, BHPCDH Protocadherin-7 chr18_61598108_y_286 286 CDH7 NM_004361 INTRON OMIM: 602988 PCDH7, BHPCDH Protocadherin-7 chr1_22395566_r_286 286 EPHA8 NM_020526 INTRON OMIM: 176945 EPHA8, EEK, HEK3 Ephrin receptor EphA8 (eph- and elk-related kinase) chr4_154742933_y_286 286 TRIM2 NM_015271 UTR OMIM: 606559 TRIM22, STAF50 Tripartite motif-containing protein 22 chr7_71086268_y_286 286 CALN1 NM_031468 INTRON chr19_13462423_r_288 288 CACNA1A NM_000068 INTRON OMIM: 601011 CACNA1A, CACNL1A4, S Calcium channel, voltage-dependent, P/Q type, alpha 1A subunit Hemiplegic migraine, familial, 141500 (3); Episodic ataxia, type 2,108500 (3); S MOUSE: 8(tg, Cacl1a4) chr19_13462423_r_288 288 CACNA1A NM_023035 INTRON OMIM: 601011 CACNA1A, CACNL1A4, S Calcium channel, voltage-dependent, P/Q type, alpha 1A subunit Hemiplegic migraine, familial, 141500 (3); Episodic ataxia, type 2,108500 (3); S MOUSE: 8(tg, Cacl1a4) chr5_36022475_r_289 289 FLJ34658 NM_152404 INTRON chr17_67166672_y_290 290 DKFZp434F2322 NM_017565 INTRON chr2_4949961_r_290 290 TSSC1 NM_003310 INTRON chr10_52732190_y_291 291 PRKG1 NM_006258 INTRON OMIM: 176894 PRKG1, PRKG1B, PRKGR Protein kinase, cGMP-dependent, regulatory, type I chr7_94756485_y_291 291 ASB4 NM_145872 INTRON OMIM: 605761 ASB4 Ankyrin repeat-containing SOCS box protein 4 MOUSE: 6(Asb4) chr7_94756485_y_291 291 ASB4 NM_016116 INTRON OMIM: 605761 ASB4 Ankyrin repeat-containing SOCS box protein 4 MOUSE: 6(Asb4) chr12_12988937_y_292 292 GPRC5D NM_018654 INTRON OMIM: 607437 GPRC5D G protein-coupled receptor, family C, group 5, member D chr7_43116289_y_293 293 KIAA0322 NM_015052 INTRON chr16_20323198_y_294 294 UMOD NM_003361 INTRON OMIM: 191845 UMOD, HNFJ, FJHN, MC Uromodulin (uromucoid, Tamm-Horsfall glycoprotein) Hyperuricemic nephropathy, familial juvenile, 162000 (3);Medullary cystic kidney MOUSE: 7(Umod) chr17_14433177_r_294 294 HS3ST3B1 NM_006041 INTRON OMIM: 604058 HS3ST3B1, 30ST3B1 Heparan sulfate D-glucosaminyl 3-0-sulfotransferase 3B1 MOUSE: 11(30st3B) chr21_31503285_r_294 294 TIAM1 NM_003253 INTRON OMIM: 600687 TIAM1 T-cell lymphoma invasion and metastasis 1 MOUSE: 16(Tiam1) chr5_21926043_y_294 294 CDH12 NM_004061 INTRON OMIM: 600562 CDH12, CDHB Cadherin-12 (N-cadherin 2) pseudogene on 5q13 in SMA region chr17_71981979_y_295 295 SDK2 NM_019064 INTRON chr7_73177291_r_300 300 CYLN2 NM_003388 INTRON OMIM: 603432 CYLN2, WBSCR4, WSCR4 Cytoplasmic linker 2 ?neurodevelpmental defect of Williams syndrome MOUSE: 5(Cyln2) chr7_73177291_r_300 300 CYLN2 NM_032421 INTRON OMIM: 603432 CYLN2, WBSCR4, WSCR4 Cytoplasmic linker 2 ?neurodevelpmental defect of Williams syndrome MOUSE: 5(Cyln2) chrX_121295157_r_300 300 GRIA3 NM_000828 INTRON OMIM: 305915 GRIA3, GLUR3 Glutamate receptor, ionotropic, AMPA 3 MOUSE: X(Glur3) chrX_121295157_r_300 300 GRIA3 NM_007325 INTRON OMIM: 305915 GRIA3, GLUR3 Glutamate receptor, ionotropic, AMPA 3 MOUSE: X(Glur3) chr12_37582224_r_301 301 LOC144402 NM_153634 INTRON chr6_39351597_y_302 302 C6orf102 NM_145027 INTRON chr9_113207893_y_302 302 TNC NM_002160 INTRON OMIM: 187380 TNC, HXB Tenascin C (hexabrachion) proximal to ABL MOUSE: 4(Hxb) chr11_83939464_y_303 303 DLG2 NM_001364 INTRON OMIM: 603583 DLG2 Discs large, Drosophila, homolog of, 2(channel-associated protein of synapses, 1 chr6_142380641_r_303 303 NMBR NM_002511 INTRON OMIM: 162341 NMBR Neuromedin B receptor chr10_67464950_y_304 304 VR22 NM_013266 INTRON chr17_33647450_r_304 304 CMYA4 NM_173167 INTRON chr1_230559210_y_304 304 KIAA1804 NM_032435 INTRON chr1_69617279_r_304 304 KIAA1365 NM_020794 INTRON chr17_40433533_r_306 306 ACLY NM_001096 INTRON OMIM: 108728 ACLY ATP citrate lyase MOUSE: ?11(Atpcl) chr20_8605426_y_306 306 PLCB1 NM_015192 INTRON chr2_163572283_y_306 306 KCNH7 NM_033272 INTRON chr2_163572283_y_306 306 KCNH7 NM_173162 INTRON chr8_57272594_r_306 306 RDH-E2 NM_138969 INTRON chr12_15557203_r_307 307 PTPRO NM_002848 INTRON OMIM: 602454 PTPRO, GLEPP1, PTPU2 Protein tyrosine phosphatase, receptor type, U chr12_15557203_r_307 307 PTPRO NM_030667 INTRON OMIM: 602454 PTPRO, GLEPP1, PTPU2 Protein tyrosine phosphatase, receptor type, U chr12_7870675_y_307 307 SLC2A14 NM_153449 INTRON chr11_10666123_r_308 308 MRVI1 NM_130385 UTR chr1_65323637_y_310 310 LEPR NM_002303 UTR OMIM: 601007 LEPR, OBR Leptin receptor Obesity, morbid, with hypogonadism (3) MOUSE: 4(Lepr) chr1_66466402_r_311 311 DKFZp761D221 NM_032291 INTRON chr14_30913864_y_312 312 AKAP6 NM_004274 INTRON chr14_93749483_y_316 316 CLMN NM_024734 INTRON chr3_186704013_r_316 316 IMP-2 NM_006548 INTRON chr21_38005152_y_317 317 KCNJ6 NM_002240 INTRON OMIM: 600877 KCNJ6, GIRK2, KCNJ7 Potassium inwardly-rectifying channel, subfamily J, member 6 MOUSE: 16(Kcnj6) chr12_102918050_r_318 318 LOC83468 NM_031302 UTR chr5_172708780_y_318 318 STC2 NM_003714 UTR chr19_56154733_r_319 319 KLK6 NM_002774 INTRON chr4_6164736_r_322 322 FLJ31564 NM_144720 INTRON chr20_38209839_y_323 323 PPP1R16B NM_015568 INTRON chr21_34168755_y_327 327 ITSN1 NM_003024 INTRON OMIM: 602442 ITSN1, SH3D1A, SH3P1 Intersectin 1 (SH3 domain protein-1A) chr19_10729915_y_328 328 DNM2 NM_004945 INTRON OMIM: 602378 DNM2 Dynamin-2 linked to Icam1 in mouse MOUSE: 9(Dnm2) chr21_29171309_r_328 328 N6AMT1 NM_013240 INTRON chr11_3881133_y_329 329 STIM1 NM_003156 INTRON OMIM: 605921 STIM1 Stromal interaction molecule 1 chrX_37176325_y_329 329 RPGR NM_000328 INTRON OMIM: 605446 RPGRIP1, LCA6, CORD9 Retinitis pigmentosa GTPase regulator-interacting protein Leber congenital amaurosis, 204000 (3); Cone-rod dystrophy 9,608194 (3) chr4_84958401_y_332 332 MGC11324 NM_032717 INTRON chr17_72895065_r_335 335 DNAI2 NM_023036 INTRON OMIM: 605483 DNAI2 Dynein, axonemal, intermediate chain 2 chrX_149439737_y_336 336 LOC139135 NM_173493 INTRON chr16_21692066_y_339 339 OTOA NM_144672 INTRON OMIM: 607038 OTOA, DFNB22 Otoancorin Deafness, autosomal recessive 22, 607039 (3) chr16_21692066_y_339 339 OTOA NM_170664 INTRON OMIM: 607038 OTOA, DFNB22 Otoancorin Deafness, autosomal recessive 22, 607039 (3) chr21_29853047_y_341 341 GRIK1 NM_175611 INTRON OMIM: 138245 GRIK1, GLUR5 Glutamate receptor, ionotropic, kainate 1 MOUSE: 16(Glur5) chr21_29853047_y_341 341 GRIK1 NM_000830 INTRON OMIM: 138245 GRIK1, GLUR5 Glutamate receptor, ionotropic, kainate 1 MOUSE: 16(Glur5) chr16_23343164_r_342 342 SCNN1B NM_000336 INTRON OMIM: 600760 SCNN1B Sodium channel, nonvoltage-gated 1, beta Liddle syndrome, 177200 (3); Pseudohypoaldosteronism, type I, 264350(3) MOUSE: 7(Scnn1b) chr12_112246063_y_344 344 SDS NM_006843 INTRON OMIM: 602877 PPP1R7, SDS22 Protein phosphatase 1, regulatory subunit 7 chr4_109971633_r_344 344 FLJ37673 NM_182591 INTRON chr11_364685_r_347 347 SIRT3 NM_012239 UTR OMIM: 604481 SIRT3, SIR2L3 Sirtuin, S. cerevisiae, homolog 3 chr3_115196464_y_348 348 DRD3 NM_000796 INTRON OMIM: 126451 DRD3 Dopamine receptor D3 {?Schizophrenia, susceptibility to} (2) chr3_115196464_y_348 348 DRD3 NM_033658 INTRON OMIM: 126451 DRD3 Dopamine receptor D3 {?Schizophrenia, susceptibility to} (2) chr3_115196464_y_348 348 DRD3 NM_033659 INTRON OMIM: 126451 DRD3 Dopamine receptor D3 {?Schizophrenia, susceptibility to} (2) chr3_115196464_y_348 348 DRD3 NM_033660 INTRON OMIM: 126451 DRD3 Dopamine receptor D3 {?Schizophrenia, susceptibility to} (2) chr3_115196464_y_348 348 DRD3 NM_033663 INTRON OMIM: 126451 DRD3 Dopamine receptor D3 {?Schizophrenia, susceptibility to} (2) chr13_31549841_r_352 352 STARD13 NM_052851 UTR chrX_1233188_y_353 353 P2RY8 NM_178129 UTR chrY_1233188_y_353 353 P2RY8 NM_178129 UTR chr20_17323433_r_355 355 PCSK2 NM_002594 INTRON OMIM: 162151 PCSK2, NEC2, PC2 Proprotein convertase subtilisin/kexin type 2 MOUSE: 2(Nec2) chr17_38030085_y_356 356 CRK7 NM_016507 INTRON chr18_3762092_y_360 360 DLGAP1 NM_004746 INTRON chr5_24191092_r_364 364 FLJ34836 NM_173668 UTR chr22_42059479_r_367 367 C22orf1 NM_001585 INTRON chr3_170511102_r_371 371 MDS1 NM_004991 INTRON OMIM: 600049 MDS1 Myelodysplasia syndrome-1 cen--EVI1--MDS1--EAP--tel Myelodysplasia syndrome-1 (3) chr11_126330634_y_376 376 NEPH2 NM_032531 INTRON OMIM: 607761 NEPH2, KIAA1867, KIR Nephrin-like 2 chr2_11275223_y_381 381 FLJ33534 NM_182586 INTRON chr19_35566342_y_382 382 KIAA0390 NM_014717 UTR chr7_126209446_r_384 384 GRM8 NM_000845 INTRON OMIM: 601116 GRM8 Glutamate receptor, metabotropic-8 chr7_138972641_r_385 385 TBXAS1 NM_001061 INTRON OMIM: 274180 TBXAS1 Thromboxane A synthase 1, platelet Thromboxane synthase deficiency (2) MOUSE: 6(Tbxas1) chr7_138972641_r_385 385 TBXAS1 NM_030984 INTRON OMIM: 274180 TBXAS1 Thromboxane A synthase 1, platelet Thromboxane synthase deficiency (2) MOUSE: 6(Tbxas1) chr13_98802058_y_387 387 PCCA NM_000282 INTRON OMIM: 232000 PCCA Propionyl Coenzyme A carboxylase, alpha polypeptide Propionicacidemia, 606054 (3) MOUSE: 14(Pcca) chr17_32571992_r_389 389 ACCN1 NM_001094 INTRON OMIM: 601784 ACCN1, BNC1, MDEG Amiloride-sensitive cation channel 1, neuronal (degenerin) chr5_168487381_r_390 390 SLIT3 NM_003062 INTRON OMIM: 603745 SLIT3, SLIL2, MEGF5 Slit, Drosophila, homolog of, 3 chr16_7279526_r_391 391 A2BP1 NM_018723 INTRON chr18_48864588_y_395 395 DCC NM_005215 INTRON OMIM: 608378 SDCCAG1 Serologically defined colon cancer antigen 1 chr1_43696485_y_396 396 SIAT6 NM_006279 INTRON OMIM: 606494 SIAT6, ST3GALII Sialyltransferase 6 chr1_43696485_y_396 396 SIAT6 NM_174963 INTRON OMIM: 606494 SIAT6, ST3GALII Sialyltransferase 6 chr1_43696485_y_396 396 SIAT6 NM_174964 INTRON OMIM: 606494 SIAT6, ST3GALII Sialyltransferase 6 chr1_43696485_y_396 396 SIAT6 NM_174965 INTRON OMIM: 606494 SIAT6, ST3GALII Sialyltransferase 6 chr1_43696485_y_396 396 SIAT6 NM_174966 INTRON OMIM: 606494 SIAT6, ST3GALII Sialyltransferase 6 chr1_43696485_y_396 396 SIAT6 NM_174967 INTRON OMIM: 606494 SIAT6, ST3GALII Sialyltransferase 6 chr1_43696485_y_396 396 SIAT6 NM_174968 INTRON OMIM: 606494 SIAT6, ST3GALII Sialyltransferase 6 chr1_43696485_y_396 396 SIAT6 NM_174969 INTRON OMIM: 606494 SIAT6, ST3GALII Sialyltransferase 6 chr1_43696485_y_396 396 SIAT6 NM_174970 INTRON OMIM: 606494 SIAT6, ST3GALII Sialyltransferase 6 chr1_43696485_y_396 396 SIAT6 NM_174971 INTRON OMIM: 606494 SIAT6, ST3GALII Sialyltransferase 6 chr1_43696485_y_396 396 SIAT6 NM_174972 INTRON OMIM: 606494 SIAT6, ST3GALII Sialyltransferase 6 chr16_23959431_y_402 402 PRKCB1 NM_002738 INTRON OMIM: 176970 PRKCB1, PKCB Protein kinase C, beta 1 polypeptide chrX_14813130_r_403 403 PIR NM_003662 INTRON OMIM: 603092 DUSP11, PIR1 Dual specificity phosphatase-11, RNA/RNP complex-interacting chr12_116171657_y_410 410 NOS1 NM_000620 INTRON OMIM: 163731 NOS1 Nitric oxide synthase 1, neuronal MOUSE: 5(Nos1) chr2_30028314_r_411 411 ALK NM_004304 INTRON OMIM: 105590 ALK Anaplastic lymphoma kinase (Ki-1) MOUSE: 17(Alk) chr4_141568102_r_411 411 MAML3 NM_018717 INTRON chr16_23998842_y_416 416 PRKCB1 NM_002738 INTRON OMIM: 176970 PRKCB1, PKCB Protein kinase C, beta 1 polypeptide chr4_152304041_r_416 416 LRBA NM_006726 INTRON chr9_69492655_r_422 422 TRPM3 NM_024971 INTRON chr4_7515236_y_424 424 SORCS2 NM_020777 INTRON OMIM: 606284 SORCS2, KIAA1329 SORCS receptor 2 chrX_90174633_y_443 443 PCDH11X NM_032968 INTRON OMIM: 300246 PCDH11X, PCDH11, PCD Protocadherin 11, X-linked chrX_90174633_y_443 443 PCDH11X NM_032969 INTRON OMIM: 300246 PCDH11X, PCDH11, PCD Protocadherin 11, X-linked chr2_88382754_y_481 481 FLJ10916 NM_018271 INTRON chr9_28179212_r_511 511 FLJ31810 NM_152570 UTR chrX_1278704_y_520 520 P2RY8 NM_178129 UTR chrY_1278704_y_520 520 P2RY8 NM_178129 UTR chr17_71255532_r_574 574 C17orf26 NM_139177 INTRON chr19_59377176_r_585 585 LENG4 NM_024298 INTRON OMIM: 606048 BB1, LENG4 Breast and bladder cancer overexpressed gene 1 chr21_40912252_r_586 586 DSCAM NM_001389 INTRON OMIM: 602523 DSCAM Down syndrome cell adhesion molecule chr16_89444729_y_706 706 DPEP1 NM_004413 INTRON OMIM: 179780 DPEP1, RDP Dipeptidase-1, renal chrX_148632921_r_753 753 CD99L2 NM_031462 INTRON chr5_11869448_r_868 868 CTNND2 NM_001332 INTRON OMIM: 604275 CTNND2, NPRAP Catenin, delta-2 Mental retardation in cri-du-chat syndrome, 123450 (2) chr7_689332_r_1303 1303 CENTA1 NM_006869 INTRON