Gene: [12p13/PTPRO] protein tyrosine phosphatase, receptor type, O; — Gene: [14p12/D14FB2S1] satellite DNA, beta, NOR2-flanking subset 1; [DNFB2S1 ]

  • Gene: [12p13/PTPRO] protein tyrosine phosphatase, receptor type, O;
  • Gene: [12p13/PXR1] peroxisome receptor 1; peroxin-5; peroxisome biogenesis disorder (MIM:601539), complementation group 2; adrenoleukodystrophy, autosomal neonatal form (MIM:202370); [PEX5 PTS1R ]
  • Gene: [12p13/SCNN1A] sodium channel, nonvoltage-gated 1 alpha; pseudohypoaldosteronism, type I (autosomal dominant; SCNN1A deficiency; MIM:177735); pseudohypoaldosteronism, type I (autosomal recessive; persian-jewish type; SCNN1A deficiency
  • Gene: [12p13/SLC6A12] solute carrier family 6 (neurotransmitter transporter, betaine/GABA), member 12; [BGT-1 ]
  • Gene: [12p13/TEAD4] TEA domain family member 4; transcriptional enhancer factor 3; transcription factor 13 (SV40 transcriptional enhancer factor)-like 1; [TEF-3 RTEF-1 ]
  • Gene: [12p13/TNFR1] tumor necrosis factor receptor 1 (55 kD); cachectin receptor 1 (lymphotoxin receptor 1);
  • Gene: [12p13/TPI] triosephosphate isomerase; nonspherocytic hemolytic anemia, Dacie's type II;
  • Gene: [12p13/UCHT3] ubiquitin carboxyl-terminal hydrolase T-3 (isopeptidase T-3);
  • Gene: [12p13/UCHT] ubiquitin carboxyl-terminal hydrolase T (isopeptidase T);
  • Gene: [12p131/APOBEC] apolipoprotein B mRNA editing enzyme, catalytic subunit;
  • Gene: [12p132/SPFCON1] salivary protein CON1; [CON1 ]
  • Gene: [12p132/SPFCON2] salivary protein CON2; [CON2 ]
  • Gene: [12p132/SPFGR1] salivary protein, histidine rich 1 (basic; Pb); [PB ]
  • Gene: [12p132/SPFGR2] salivary protein, histidine rich 2 (basic; post-Pb); [PPB ]
  • Gene: [12p132/SPFPRB1] salivary proline-rich basic protein 1 (BstNI subfamily); [PRB1 ]
  • Gene: [12p132/SPFPRB2] salivary proline-rich basic protein 2 (BstNI subfamily); [PRB2 ]
  • Gene: [12p132/SPFPRB3] salivary proline-rich basic protein 3 (BstNI subfamily); parotid salivary glycoprotein G1; [PRB3 G1 ]
  • Gene: [12p132/SPFPRB4] salivary proline-rich basic protein 4 (BstNI subfamily); [PRB4 ]
  • Gene: [12p132/SPFPRH1] salivary proline-rich acidic protein 1 (HaeIII subfamily); dental caries in children; [PRH1 PA DB ]
  • Gene: [12p132/SPFPRH2] salivary proline-rich acidic protein 2 (HaeIII subfamily); [PRH2 PR ]
  • Gene: [12p132/SPFU10] salivary undefined family protein Pu10;
  • Gene: [12p132/SPFU11] salivary undefined family protein Pu11;
  • Gene: [12p132/SPFU12] salivary undefined family protein Pu12;
  • Gene: [12p132/SPFU13] salivary undefined family protein Pu13;
  • Gene: [12p132/SPFU14] salivary undefined family protein Pu14;
  • Gene: [12p132/SPFU15] salivary undefined family protein Pu15;
  • Gene: [12p132/SPFU1] salivary undefined family protein Pu1;
  • Gene: [12p132/SPFU2] salivary undefined family protein Pu2;
  • Gene: [12p132/SPFU3] salivary undefined family protein Pu3;
  • Gene: [12p132/SPFU4] salivary undefined family protein Pu4;
  • Gene: [12p132/SPFU5] salivary undefined family protein Pu5;
  • Gene: [12p132/SPFU6] salivary undefined family protein Pu6;
  • Gene: [12p132/SPFU7] salivary undefined family protein Pu7;
  • Gene: [12p132/SPFU8] salivary undefined family protein Pu8;
  • Gene: [12p132/SPFU9] salivary undefined family protein Pu9;
  • Gene: [12p132/SPFUC] salivary undefined family protein Pc (proline-rich); parotid salivary protein variant Pc (proline-rich); [PCS PC ]
  • Gene: [12p132/SPFUO] salivary undefined family protein Po; parotid salivary protein variant Po; [PO ]
  • Gene: [12p132/SPFUS] salivary undefined family protein Ps (size variant); parotid salivary protein variant Ps (size variant); [PS ]
  • Gene: [12p133/FKHL16] forkhead (Drosophila)-like 16 (trident); [HFH-11 ]
  • Gene: [12p133/LAG3] lymphocyte-activation gene 3;
  • Gene: [12p133/LAMP1L1] lysosome-associated membrane protein 1-like 1; glycoprotein LAMP-1-like 1;
  • Gene: [12p133/RBBP2] retinoblastoma-binding protein 2;
  • Gene: [12p133/SLC2A3] solute carrier family 2 (facilitated glucose transporter), member 3; glucose transporter 3 (fetal skeletal muscle); [GLUT3 ]
  • Gene: [12p1331/DRPLA] dentatorubral-pallidoluysian atrophy protein; dentatorubral-pallidoluysian atrophy; myoclonus epilepsy with choreoathetosis (Naito-Oyanagi disease);
  • Gene: [12q/ACACB] acetyl-Coenzyme A carboxylase beta (275kD; EC:6.4.1.2); biotin carboxylase (EC:6.3.4.14);
  • Gene: [12q/DDIT1L] DNA-damage-inducible transcript 1-like;
  • Gene: [12q/ENUR2] enuresis, nocturnal 2;
  • Gene: [12q/H1F4] H1 histone family, member 4;
  • Gene: [12q/LAMRL2] laminin receptor-like 2;
  • Gene: [12q/MSK27] antigen MSK27 (monoclonal antibody MG6);
  • Gene: [12q/MSK36] antigen MSK36 (monoclonal antibody CNT/11);
  • Gene: [12q/MSK7] antigen MSK7 (monoclonal antibody VI);
  • Gene: [12q/MYPT1] myosin phosphatase target subunit 1 (myosin-binding); [MBS ]
  • Gene: [12q/PTPRB] protein tyrosine phosphatase, receptor type, beta polypeptide;
  • Gene: [12q/RPL41] ribosomal protein L41;
  • Gene: [12q/RPLP0] ribosomal protein, large, P0; [PRLP0 ]
  • Gene: [12q/RPS26] ribosomal protein S26;
  • Gene: [12q/SYT1] synaptotagmin 1 (p65); [SYT ]
  • Gene: [12q/TAC3] tachykinin 3 (neurokinin B, neurokinin beta, neuromedin K); [NKNB ]
  • Gene: [12q1/ADCY6] adenylate cyclase 6;
  • Gene: [12q1/ALDL1] adrenoleukodystrophy-like 1; [ALDR ]
  • Gene: [12q1/ALLR] ALL1-related gene (MLL-related); acute leukemia?; [ALR ]
  • Gene: [12q1/ARVPR1A] arginine vasopressin receptor 1A; [AVPR1A]
  • Gene: [12q1/CD63] antigen CD63 (ME491; melanoma 1 antigen); [MLA1 ME491 ]
  • Gene: [12q1/CNTN1] contactin 1 (gp135);
  • Gene: [12q1/GAS41] glioma amplified sequence; glioma, type ?;
  • Gene: [12q1/GCN5L1] GCN5 (general control of amino-acid synthesis, yeast, homolog)-like 1; [RT14 ]
  • Gene: [12q1/GGTA1P] glycoprotein, alpha-galactosyltransferase 1 pseudogene; [GLYT3 ]
  • Gene: [12q1/GSTPP] glutathione S-transferase pi pseudogene; [GST3L GSTPL ]
  • Gene: [12q1/HIVE1] human immunodeficiency virus type 1 expression (elevated); [IVE1 ]
  • Gene: [12q1/HOXC10] homeo box C10; [HOX3I ]
  • Gene: [12q1/HOXC11] homeo box C11(3H), homologous to mouse Hox-3.8; [HOX3H ]
  • Gene: [12q1/HOXC12] homeo box C12(3F); [HOX3F ]
  • Gene: [12q1/HOXC13] homeo box C13(3G), homologous to mouse Hox-3.7; [HOX3G ]
  • Gene: [12q1/HOXC4] homeo box C4(3E); [HOX3E ]
  • Gene: [12q1/HOXC5] homeo box C5(3D), homologous to mouse Hox-6.2; [HOX3D ]
  • Gene: [12q1/HOXC6] homeo box C6(3C), homologous to mouse Hox-6.1; [HOX3C ]
  • Gene: [12q1/HOXC8] homeo box C8(3A), homologous to mouse Hox-3.1; [HOX3 HOX3A ]
  • Gene: [12q1/HOXC9] homeo box C9(3B), homologous to mouse Hox-3.2; [HOX3B ]
  • Gene: [12q1/ITGA5] integrin, alpha 5 (alpha F; antigen CD49E); fibronectin receptor, alpha polypeptide; [VLA5A CD49E ]
  • Gene: [12q1/KRT1L1] keratin 1, type II, like 1; [KRTL1 ]
  • Gene: [12q1/KRT1] keratin 1, type II, beta, basic (keratin H; hair alpha protein; pI 7.8; 67kD); epidermolytic hyperkeratosis (bullous congenital ichthyosiform erythroderma; MIM:113800); [KRTA K1 KRTH ]
  • Gene: [12q1/KRT2A] keratin 2A, type II, beta, basic (epidermal; pI 7.8; 65.5kD); epidermal ichthyosis bullosa of Siemens (MIM:146800); [CYKB2 KRT2 ]
  • Gene: [12q1/KRT3] keratin 3, type II, beta, basic; [CYKB3 ]
  • Gene: [12q1/KRT5] keratin 5, type II, beta, basic (pI 7.4; 58kD); epidermolysis bullosa simplex (Dowling-Meara type; MIM:131760); epidermolysis bullosa simplex (Weber-Cockayne type; MIM:131800); epidermolysis bullosa simplex (EBS2; generali
  • Gene: [12q1/KRT6A] keratin 6, type II, beta, basic (pI 7.8; 56kD); pachyonychia, congenita (Jadassohn-Lewandowsky type; MIM:167200); [CYKB6 KRT6 ]
  • Gene: [12q1/KRT7] keratin 7, type II, beta, basic (simple epithelial; pI 6.0; 55kD); [CYKB7 ]
  • Gene: [12q1/KRT8] keratin 8, type II, beta, basic (pI 6.1; 53kD); [CYKB8 ]
  • Gene: [12q1/KRTHB3] keratin, hair, basic, 3; hard keratin, type II, 3; [Hb-3 ]
  • Gene: [12q1/KRTHB5] keratin, hair, basic, 5; hard keratin, type II, 5; [Hb-5 ]
  • Gene: [12q1/LIPO] lipomatosis, multiple, familial; breakpoint associated with benign lipoma; [BABL ]
  • Gene: [12q1/LRP1] low density lipoprotein receptor-related protein 1; alpha-2-macroglobulin receptor; apolipoprotein E receptor; [APR APOER ]
  • Gene: [12q1/MSK4] antigen MSK4 (monoclonal antibody A123/A127); [MSK7VI ]
  • Gene: [12q1/MYO1A] myosin IA;
  • Gene: [12q1/NAB2] NGFI-A binding protein 2 (EGR1 binding protein 2);
  • Gene: [12q1/PABPL2] poly(A)-binding protein-like 2;
  • Gene: [12q1/PPKB] palmoplantar keratoderma, diffuse non-epidermolytic Bothnian type;
  • Gene: [12q1/PRPH] peripherin;
  • Gene: [12q1/PSA] pleomorphic salivary gland adenoma; [SGPA ]
  • Gene: [12q1/RDH5] retinol dehydrogenase 5 (11-cis and 9-cis);
  • Gene: [12q1/SAS] sarcoma amplified sequence;
  • Gene: [12q1/SHMT2] serine hydroxymethyltransferase 2 (mitochondrial);
  • Gene: [12q1/SILV] silver (mouse homolog)-like; melanocyte protein mel 17; [SIL Pmel17 ]
  • Gene: [12q1/TARB2] TAR (HIV) RNA-binding protein 2; [TARBP2 ]
  • Gene: [12q1/TEGT] testis enhanced gene transcript;
  • Gene: [12q1/ULR] uterine leiomyoma breakpoint region;
  • Gene: [12q1/VDR] vitamin D receptor (VD-resistant rickets, type IIA); vitamin D-resistant rickets, type IIA (MIM:277440); vitamin D-resistant rickets, type IIB (MIM:277440); [VDDR2A VDRR2 ]
  • Gene: [12q12/ACCN2] amiloride-sensitive cation channel 2, neuronal; brain sodium channel 2; [BNAC2 ]
  • Gene: [12q12/UBE2L2] ubiquitin-conjugating enzyme E2L 2;
  • Gene: [12q13/ACVRLK1] activin A receptor, type II-like kinase 1; activin A receptor, type II-like 1; Osler-Rendu-Weber syndrome 2 (ORW2; MIM:600376); telangiectasia, hereditary hemorrhagic, type II (HHT2; MIM:600376);
  • Gene: [12q13/AMHR2] anti-Mullerian hormone receptor, type II (serine/threonine kinase); persistent Mullerian duct syndrome, type II (pseudohermaphroditism, male internal; MIM:261550);
  • Gene: [12q13/AQP2] aquaporin 2 (collecting duct); diabetes insipidus, nephrogenic, autosomal recessive (MIM:222000);
  • Gene: [12q13/AQP5] aquaporin 5;
  • Gene: [12q13/AQP6] aquaporin 6, kidney specific; [AQP2L ]
  • Gene: [12q13/ARF3] ADP-ribosylation factor 3;
  • Gene: [12q13/ART4] ADP-ribosyltransferase 4;
  • Gene: [12q13/ATF1] activating transcription factor 1; tax-responsive enhancer element B36; [TREB36 ]
  • Gene: [12q13/CACNB3] calcium channel, voltage-dependent, beta 3 subunit; calcium channel, L type, beta 3 polypeptide; [CACNLB3 ]
  • Gene: [12q13/CDK2] cyclin-dependent kinase 2 (p34; homolog of Xenopus Eg1);
  • Gene: [12q13/CDK4] cyclin-dependent kinase 4;
  • Gene: [12q13/DDIT3] DNA-damage-inducible transcript 3 (c/ebp-homologous protein); growth arrest and DNA damage-inducible gene GADD153; myxoid liposarcoma; [CHOP GADD153 ]
  • Gene: [12q13/EGFR3] avian erythroblastic leukemia viral (v-erb-b2) oncogene homolog 3; oncogene homolog ERBB3; protein tyrosine kinase, receptor ERBB3;
  • Gene: [12q13/FXR1] fragile X mental retardation gene - autosomal homolog 1;
  • Gene: [12q13/GLI1] chromatin-associated GLI-phosphoprotein 1 (oncogene GLI); zinc finger oncoprotein GLI1; oncogene GLI (glioma-associated oncogene homolog); GLI-Kruppel family member GLI1 (oncogene GLI); glioblastoma multiform (astrocytoma
  • Gene: [12q13/HMR] hormone receptor (growth factor inducible nuclear protein N10); nuclear protein N10, growth factor inducible (hormone receptor); [NP10 N10 ]
  • Gene: [12q13/HPV18I2] human papillomavirus (type 18) integration site 2;
  • Gene: [12q13/ITGA7] integrin, alpha 7;
  • Gene: [12q13/KRT18] keratin 18, type I, alpha, acidic (simple epithelial; pI 5.7; 44kD); [CYKA18 ]
  • Gene: [12q13/KRTHB1] keratin, hair, basic, 1; hard keratin, type II, 1; [Hb-1 ]
  • Gene: [12q13/KRTHB6] keratin, hair, basic, 6; hard keratin, type II, 6; monilethrix (alopecia; MIM:158000); [MNX Hb-6 ]
  • Gene: [12q13/LALBA] alpha-lactalbumin;
  • Gene: [12q13/MIP] major intrinsic protein of lens fiber;
  • Gene: [12q13/NFE2] nuclear factor, erythroid-derived 2, 45kD;
  • Gene: [12q13/NRAMP2] natural resistance-associated macrophage protein 2;
  • Gene: [12q13/PA2G4] proliferation-associated 2G4, 38kD;
  • Gene: [12q13/RAB13] oncogene RAS-family, member rab13;
  • Gene: [12q13/RAB5B] oncogene RAS-family, member rab5B;
  • Gene: [12q13/RARG] retinoic acid receptor, gamma;
  • Gene: [12q13/SCN8A] sodium channel, voltage-gated, type VIII, alpha polypeptide; motor endplate disease in mouse; [MED ]
  • Gene: [12q13/SMARCC2] SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily c, member 2; chromatin remodeling complex, BRG1-associated factor, 170kD; [BAF170 ]
  • Gene: [12q13/SMARCD1] SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily d, member 1; chromatin remodeling complex, BRG1-associated factor, 60kD, A; [BAF60A CRACD1 ]
  • Gene: [12q13/TFCP2] transcription factor CP2; [CP2 ]
  • Gene: [12q13/WNT1] wingless-type MMTV integration site 1; murine mammary tumor virus integration site homolog 1; [INT1 ]
  • Gene: [12q13/ZNF75B] zinc finger protein 75B pseudogene;
  • Gene: [12q13/ZPK] zipper (leucine) protein kinase;
  • Gene: [12q131/COL2A1] collagen, type II, alpha 1; chondrocalcin; primary osteoarthritis; spondyloepiphyseal dysplasia, congenital type (MIM:183900); achondrogenesis-hypogenesis type II (MIM:200610); osteoarthritis with mild chondrodysplasia
  • Gene: [12q131/FRA12A] fragile site 12q13.1, folic acid type, rare;
  • Gene: [12q131/HEM1] hematopoietic protein 1;
  • Gene: [12q131/HNRPA1] heterogeneous nuclear ribonucleoprotein A1 (34 kD); RNP particle, heterogeneous nuclear, A1 protein (34 kD);
  • Gene: [12q131/INHBC] inhibin, beta C;
  • Gene: [12q131/ITGB7] integrin, beta 7;
  • Gene: [12q131/NELL2] nel (chicken)-like 2 protein; [NRP ]
  • Gene: [12q131/PCBP2] poly(rC)-binding protein 2;
  • Gene: [12q131/PRKAG1] protein kinase, AMP-activated, gamma 1 non-catalytic subunit (AMPK gamma 1);
  • Gene: [12q131/SP1] Sp1 transcription factor;
  • Gene: [12q131/WNT10B] wingless-type MMTV integration site 10B, human homolog;
  • Gene: [12q133/CYP27B1] cytochrome P450, subfamily XXVIIB (25-hydroxyvitamin D3-1-alpha-hydroxylase), polypeptide 1; pseudovitamin D deficiency rickets (vitamin D dependency 1);
  • Gene: [12q133/DGKA] diacylglycerol kinase, alpha (80kD);
  • Gene: [12q133/GALGT] beta-1,4 N-acetylgalactosaminyltransferase;
  • Gene: [12q14/GNS] N-acetylglucosamine-6-sulfatase; mucopolysaccharidosis type IIID (N-acetylglucosamine-6-sulfatase deficiency); SanFillippo syndrome D (N-acetylglucosamine-6-sulfatase deficiency);
  • Gene: [12q14/MMP19] matrix metalloproteinase 19;
  • Gene: [12q14/OAP] osteoarthrosis, precocious;
  • Gene: [12q14/RAP1B] RAS-related protein RAP-1B (K-rev);
  • Gene: [12q15/CPM] carboxypeptidase M;
  • Gene: [12q15/HMGIC] high-mobility group (nonhistone chromosomal) protein isoform I-C;
  • Gene: [12q15/MDM2] mouse double minute 2, human homolog of; p53-binding protein;
  • Gene: [12q15/PSMC6] proteasome (prosome, macropain) 26S subunit, ATPase, 6; 26S protease regulatory subunit S10B (p42);
  • Gene: [12q2/ACADS] acyl-CoA dehydrogenase S (FA short straight-chain C2/C6); butyryl-CoA dehydrogenase (ethylen reductase); lipid-storage myopathy, secondary to SCADh deficiency;
  • Gene: [12q2/ATP2A2] ATPase, Ca++ transporting, cardiac muscle, slow twitch 2; sarcoplasmic reticulum Ca(2+)-ATPase 2;
  • Gene: [12q2/ATP2B1] ATPase, Ca++ transporting, plasma membrane 1;
  • Gene: [12q2/CART1] cartilage-specific homeobox protein;
  • Gene: [12q2/CLTA] clathrin, light polypeptide (Lca);
  • Gene: [12q2/CRY1] cryptochrome 1 (photolyase-like); [PHLL1 ]
  • Gene: [12q2/DAR] Darier-White disease (keratosis follicularis);
  • Gene: [12q2/DUSP6] dual specificity phosphatase 6 (EC:3.1.3.48 and EC:3.1.3.16); MAP kinase phosphatase 3;
  • Gene: [12q2/EPS8] epidermal growth factor receptor pathway substrate 8 (97kD);
  • Gene: [12q2/HAL] histidine ammonia-lyase (histidinemia); histidinemia (histidase deficiency);
  • Gene: [12q2/LUM] lumican (keratan sulfate proteoglycan); [LDC ]
  • Gene: [12q2/MYL2] myosin, light polypeptide 2, regulatory, cardiac, slow;
  • Gene: [12q2/NACA] nascent-polypeptide-associated complex alpha polypeptide;
  • Gene: [12q2/NFYB] nuclear factor binding to Y box of HLA genes, beta polypeptide; transcription factor NF-Y, B subunit;
  • Gene: [12q2/NS1] Noonan syndrome 1; Turner phenotype with normal karyotype (pterygium colli syndrome);
  • Gene: [12q2/PLA2G1B] phospholipase A2, group IB (pancreas);
  • Gene: [12q2/PMCH] pro-melanin-concentrating hormone;
  • Gene: [12q2/RPL6] ribosomal protein L6; tax-responsive enhancer element binding protein 107; [TXREB107 ]
  • Gene: [12q2/TSC3] tuberous sclerosis 3;
  • Gene: [12q2/TXNRD1] thioredoxin reductase 1;
  • Gene: [12q2/UNG1] uracil-DNA glycosylase 1;
  • Gene: [12q21/CENPC2] centromere protein C pseudogene;
  • Gene: [12q21/CNA2] cornea plana 2 (autosomal recessive);
  • Gene: [12q21/DSPG3] dermatan sulphate proteoglycan 3; [Pg-Lb ]
  • Gene: [12q21/MYF5] myogenic factor 5;
  • Gene: [12q21/MYF6] myogenic factor 6 (herculin); muscle regulatory factor 4; [MRF4 ]
  • Gene: [12q21/NDUFB8] NADH dehydrogenase (ubiquinone) 1 beta subcomplex, 8 (19kD, ASHI);
  • Gene: [12q21/NTS] neurotensin;
  • Gene: [12q21/PEPB] peptidase B;
  • Gene: [12q21/PIGAP1] phosphatidylinositol glycan, class A, pseudogene 1;
  • Gene: [12q211/CSRP2] cysteine and glycine-rich protein 2; LIM domain only 5 (smooth muscle); [CRP2 SmLIM ]
  • Gene: [12q213/FRA12B] fragile site 12q21.3, aphidicolin type, common;
  • Gene: [12q22/BTG1] B-cell translocation gene 1, anti-proliferative;
  • Gene: [12q22/LTA4H] leukotriene A4 hydrolase;
  • Gene: [12q22/MGF] mast cell growth factor;
  • Gene: [12q22/NEDD1] neural precursor cell expressed, developmentally down-regulated 1;
  • Gene: [12q22/TMPO] thymopoietin; [TP ]
  • Gene: [12q22/ZNF144] zinc finger protein 144 (DNA binding protein Mel-18);
  • Gene: [12q23/DCN] decorin (proteoglycan PG-40); [PG-40 PGII ]
  • Gene: [12q23/ELK3] ELK3, ETS-domain protein (serum response factor (SRF) accessory protein 2); [SAP2 ]
  • Gene: [12q23/IGF1] insulin-like growth factor 1 (somatomedin C); pygmy dwarfism (somatomedin C deficiency?, IGF1 deficiency?); growth retardation with sensorineural deafness and mental retardation; [SMC ]
  • Gene: [12q24/ALFN1] activator of liver function 1 (hepatic phenotype restoration inducing sequence); [HALF1 ]
  • Gene: [12q24/BDC] brachydactyly, type C;
  • Gene: [12q24/DAO] D-amino-acid oxidase;
  • Gene: [12q24/FRA12E] fragile site 12q24, aphidicolin type, common;
  • Gene: [12q24/HPD] 4-hydroxyphenylpyruvate dioxygenase; tyrosinemia, type III (4-hydroxyphenylpyruvate dioxygenase);
  • Gene: [12q24/PPP1CC] protein phosphatase 1, catalytic subunit, gamma isoform;
  • Gene: [12q24/PRKAB1] protein kinase, AMP-activated, beta 1 non-catalytic subunit (AMPK beta 1);
  • Gene: [12q24/PXN] paxillin (focal adhesion protein);
  • Gene: [12q24/RFC5] replication factor C (activator 1) 5 (36.5kD);
  • Gene: [12q24/RPL21P] ribosomal protein L21 pseudogene;
  • Gene: [12q24/SELPLG] selectin P ligand; antigen CD162; [PSGL1 ]
  • Gene: [12q24/TRA1] tumor rejection antigen (gp96) 1;
  • Gene: [12q241/ASCL1] achaete-scute complex (Drosophila)-like transcription factor 1; [ASH1 ]
  • Gene: [12q241/BCL7] B-cell chronic lymphatic leukemia 7 (B-CLL: lymphoma 7);
  • Gene: [12q241/IFNG] interferon, gamma;
  • Gene: [12q241/PAH] phenylalanine hydroxylase; phenylketonuria (phenylalanine hydroxylase deficiency);
  • Gene: [12q241/PTPN11] protein tyrosine phosphatase, non-receptor type 11;
  • Gene: [12q241/SCA2] ataxin 2; spinocerebellar ataxia 2 (olivopontocerebellar ataxia 2; MIM:183090); [ATX2 ]
  • Gene: [12q241/TBX3] T-box 3; ulnar mammary syndrome (UMS; MIM:181450); [UMS ]
  • Gene: [12q241/TBX5] T-box 5; Holt-Oram syndrome (HOS; MIM:142900); [HOS ]
  • Gene: [12q2413/FRA12D] fragile site 12q24.13, folic acid type, rare;
  • Gene: [12q242/ALDH2] aldehyde dehydrogenase 2, liver mitochondrial; alcohol abuse inhibitory factor (alcohol sensitivity);
  • Gene: [12q242/FRA12C] fragile site 12q24.2, BrdU type, common;
  • Gene: [12q242/NOS1] nitric oxide synthase 1 (neuronal);
  • Gene: [12q242/OAS1] interferon-inducible 42kD 2-5a synthetase; 2',5'-oligoisoadenylate synthetase;
  • Gene: [12q242/OAS2] 2'-5'oligoadenylate synthetase 2;
  • Gene: [12q242/OAS3] 2'-5'oligoadenylate synthetase 3;
  • Gene: [12q243/MUC8] mucin 8, tracheobronchial;
  • Gene: [12q243/NHP2L1] non-histone chromosome protein 2 (S. cerevisiae)-like 1;
  • Gene: [12q243/POLE] polymerase (DNA directed), epsilon;
  • Gene: [12q243/PSMD9] proteasome (prosome, macropain) 26S subunit, non-ATPase, 9;
  • Gene: [12q243/RSN] restin (Reed-Steinberg cell expressed intermediate filament-associated protein); Hodgkin disease, associated protein;
  • Gene: [12q243/TCF1] transcription factor 1, hepatic; LF-B1, albumin proximal factor; hepatic nuclear factor 1 (HNF1); maturity onset diabetes of the young 3 (MIM:600496); non-insulin-dependent diabetes mellitus (common, type 2) 2 (MIM:60140
  • Gene: [12q243/UBC] ubiquitin, gene-C subfamily, nonameric polyprotein;
  • Gene: [12q243/ZNF140] zinc finger protein 140 (clone pHZ-39);
  • Gene: [12q2431/DOC1] deleted in oral cancer 1 (tumor suppressor);
  • Gene: [12q2432/P2RX4] purinergic receptor P2X, ligand-gated ion channel, 4 (purinoceptor P2X4); [P2X4 ]
  • Gene: [12q2433/ZNF10] zinc finger protein 10 (KOX 1); [KOX1 ]
  • Gene: [12q2433/ZNF26] zinc finger protein 26 (KOX 20); [KOX20 ]
  • Gene: [12^/AD5] Alzheimer disease 5;
  • Gene: [12^/APOF] apolipoprotein F;
  • Gene: [12^/ASSP14] argininosuccinate synthetase pseudogene 14;
  • Gene: [12^/ATP5B] ATP synthase, H+ transporting, mitochondrial F1 complex, beta polypeptide;
  • Gene: [12^/CCNT1] cyclin T1 (CDK9-associated C-type cyclin);
  • Gene: [12^/CD36L1] antigen CD36 (collagen type I receptor, thrombospondin receptor)-like 1; CD36 and LIMPII analogous 1; scavenger receptor, class B, type I; [CLA1 SRBI ]
  • Gene: [12^/COX5BL5] cytochrome c oxidase subunit Vb-like 5;
  • Gene: [12^/CS] citrate synthase;
  • Gene: [12^/ERVF3] endogenous retroviral sequence, full length 3 (band F21, 3.5 kb); [FRV3 ]
  • Gene: [12^/ERVT3] endogenous retroviral sequence, truncated 3 (band T3, 17.8 kb);
  • Gene: [12^/FEOM1] fibrosis of the extraocular muscles, congenital; [FEOM ]
  • Gene: [12^/GPD1] glycerol-3-phosphate dehydrogenase 1 (alpha, soluble);
  • Gene: [12^/GSTMS1] glutathione S-transferase, microsomal, 1;
  • Gene: [12^/HTR1DP1] 5-hydroxytryptamine (serotonin) receptor 1D pseudogene 1;
  • Gene: [12^/IGFB6] insulin-like growth factor binding protein 6; [IGFBP6 IBP6 ]
  • Gene: [12^/KCNA2] potassium voltage-gated channel, shaker-related subfamily, member 2;
  • Gene: [12^/KRT4] keratin 4, type II, beta, basic (pI 7.3; 59kD); [CYKB4 CYK4 ]
  • Gene: [12^/KRT6B] keratin 6B, type II, beta, basic;
  • Gene: [12^/LYZ] lysozyme; amyloidosis VIII (systemic nonneuropathic, Ostertag type, German type; MIM:105200);
  • Gene: [12^/MARS] methionyl-tRNA synthetase;
  • Gene: [12^/MVK] mevalonate kinase (mevalonic aciduria); mevalonic aciduria;
  • Gene: [12^/MYBPC1] myosin-binding protein C, slow-type;
  • Gene: [12^/PFKX] phosphofructokinase, polypeptide X;
  • Gene: [12^/PHC] phosphate carrier, mitochondrial;
  • Gene: [12^/POU6F1] POU domain, class 6, transcription factor 1; [BRN5 MPOU ]
  • Gene: [12^/PYHG10] protein spot in 2-D gels (MM 77 kD);
  • Gene: [12^/PYHG19] protein spot in 2-D gels (MM 12 kD);
  • Gene: [12^/PYHG6] protein spot in 2-D gels (MM 85 kD);
  • Gene: [12^/S8] surface antigen S8 (chromosome 12); [SA12-1 ]
  • Gene: [12^/TUBAC] tubulin, alpha, isotype C (constitutive); [TUBAL1 TUBA ]
  • Gene: [12^/VDAC3] voltage-dependent anion channel 3;
  • Gene: [13p111/D13Z1] satellite DNA, alpha, aRI(680) subset;
  • Gene: [13p111/D13Z2] satellite DNA, alpha, aXI(1020) subset (probe pTRA-1);
  • Gene: [13p111/D13Z3] satellite DNA, alpha (probe pTRA-4);
  • Gene: [13p111/D13Z4] satellite DNA, alpha (probe pTRA-2);
  • Gene: [13p111/D13Z5] satellite DNA, alpha (probe pTR9-H2/pTR9);
  • Gene: [13p111/D13Z6] satellite DNA, alpha (probe pTRA-7);
  • Gene: [13p12/D13FB2S1] satellite DNA, beta, NOR1-flanking subset 1; [D13F39S1 ]
  • Gene: [13p12/D13FB2S2] satellite DNA, beta, NOR1-flanking subset 2; [DNFB2S2 ]
  • Gene: [13p12/RNR1BAM] rDNA subset 1, BamHI-RFLP in downstream 28S rRNA gene (30-50 copies); [RNR1 ]
  • Gene: [13p12/RNR1SN1] RNA, ribosomal 1, 8S-1 RNA (sn-PolI; 30-50 copies); [RNR1 SNPIRNA1 ]
  • Gene: [13p12/RNR1SN2] RNA, ribosomal 1, 8S-2 RNA (sn-PolI; 30-50 copies); [RNR1 SNPIRNA2 ]
  • Gene: [13p12/RNR1UA] RNA, ribosomal 1, accessory unit 5.8S rRNA (30-50 copies); [RNR1 ]
  • Gene: [13p12/RNR1UL] RNA, ribosomal 1, large unit 28S rRNA (30-50 copies); [RNR1 ]
  • Gene: [13p12/RNR1US] RNA, ribosomal 1, small unit 18S rRNA (30-50 copies); [RNR1 ]
  • Gene: [13p13/D13Z7] satellite DNA, unknown class (probe ?);
  • Gene: [13q/ALDRL4] aldehyde reductase (aldose reductase)-like 4;
  • Gene: [13q/CLN5] ceroid-lipofuscinosis, neuronal 5;
  • Gene: [13q/CZP3] cataract, zonular pulverulent 3;
  • Gene: [13q/GPR38] G protein-coupled receptor 38;
  • Gene: [13q/HTR2A] 5-hydroxytryptamine (serotonin) receptor 2A; schizophrenia, associated to HTR2A; [HTR2 ]
  • Gene: [13q/PAPA2] postaxial polydactyly, type A2;
  • Gene: [13q1/ATP1AL1] ATPase, Na+,K+ transporting, alpha polypeptide-like 1;
  • Gene: [13q1/BRCA2] oncogene BRCA2; breast cancer 2, early onset;
  • Gene: [13q1/ED2] ectodermal dysplasia 2, hidrotic (Clouston syndrome); [HED ]
  • Gene: [13q1/ENUR1] enuresis, nocturnal 1;
  • Gene: [13q1/FAB3P] fatty acid binding protein 3 pseudogene; [FABP3P ]
  • Gene: [13q1/FGF9] fibroblast growth factor 9 (glia-activating factor);
  • Gene: [13q1/GJA3] gap junction protein, alpha 3, 46kD (connexin 46); [CX46 ]
  • Gene: [13q1/GTF3A] general transcription factor IIIA; [TFIIIA ]
  • Gene: [13q1/MADH9] MAD (mothers against decapentaplegic, Drosophila) homolog 9; [SMAD9 ]
  • Gene: [13q1/PABPL3] poly(A)-binding protein-like 3;
  • Gene: [13q1/PTPN2P2] protein tyrosine phosphatase, non-receptor type 2 (pseudogene 2);
  • Gene: [13q1/RFC3] replication factor C (activator 1) 3 (38kD);
  • Gene: [13q1/TUBBP2] tubulin, beta, pseudogene 2;
  • Gene: [13q1/ZNF198] zinc finger protein 198; stem-cell leukemia/lymphoma syndrome; [SCLL ]
  • Gene: [13q11/GJB2] gap junction protein, beta 2, 26 kD (connexin 26); deafness, autosomal dominant 3 (DFNA3; MIM:601544); deafness, autosomal recessive 1 (DFNB1; MIM:220290); [CX26 NSRD1 ]
  • Gene: [13q11/TUBA2] tubulin, alpha 2;
  • Gene: [13q12/FLT1] oncogene FLT1 (src/ros/fms-related tyrosine kinase); fms-related tyrosine kinase 1;
  • Gene: [13q12/FLT3] oncogene FLT3 (src/ros/fms-related tyrosine kinase); fms-related tyrosine kinase 3;
  • Gene: [13q12/FTHL7] ferritin, heavy polypeptide-like 7;
  • Gene: [13q12/GAPDL14] glyceraldehyde-3-phosphate dehydrogenase-like 14;
  • Gene: [13q12/GPR12] G protein-coupled receptor 12;
  • Gene: [13q12/HMG1L] high-mobility group (nonhistone chromosomal) protein 1-like;
  • Gene: [13q12/HMG1] high-mobility group (nonhistone chromosomal) protein 1;
  • Gene: [13q12/MIPEP] mitochondrial intermediate peptidase;
  • Gene: [13q12/RPL23P] ribosomal protein L23 pseudogene;
  • Gene: [13q12/SGCG] sarcoglycan, gamma (dystrophin associated glycoprotein, 35kD); limb girdle muscular dystrophy 2C (autosomal recessive); Duchenne-like muscular dystrophy, autosomal recessive 1; [DAGA4 LGMD2C ]
  • Gene: [13q12/TDPX1] thioredoxin-dependent peroxide reductase 1; thiol-specific antioxidant 1; natural killer-enhancing factor B;
  • Gene: [13q121/ESRRAP] estrogen-related receptor alpha pseudogene;
  • Gene: [13q121/IPF1] insulin promoter factor 1, homeodomain transcription factor; pancreatic agenesis, congenital (MIM:260370); pancreatic agenesis, dorsal (MIM:167755); [IDX-1 STF-1 ]
  • Gene: [13q121/RPL21] ribosomal protein L21;
  • Gene: [13q122/MBS] Moebius syndrome (congenital facial dysplegia);
  • Gene: [13q123/CDX2] caudal type homeo box transcription factor 2; caudal type homeo box transcription factor 3; [CDX3 ]
  • Gene: [13q123/SLC7A1] solute carrier family 7 (cationic amino acid transporter, y+ system), member 1; amino acid transporter, cationic 1 (high-affinity); [ATRC1 CAT-1 ]
  • Gene: [13q13/CSNK1A1] casein kinase 1, alpha 1 polypeptide;
  • Gene: [13q13/MAB21L1] mab-21 (C.elegans)-like 1 protein; [CAGR1 ]
  • Gene: [13q132/FRA13A] fragile site 13q13.2, aphidicolin type, common;
  • Gene: [13q14/CTSBL] cathepsin B-like;
  • Gene: [13q14/DBM] tumor supressor DBM (putative; disrupted in B-cell malignancy); B-cell malignancy, low grade; leukemia, chronic lymphocytic, B-cell;
  • Gene: [13q14/GTF2F2] general transcription factor IIF, polypeptide 2 (30kD subunit);
  • Gene: [13q14/IGHEE] immunoglobulin-E expression regulator (basal serum level); atopic IgE responsiveness (allergic asthma and rhinitis?); [IGHER IGEL ]
  • Gene: [13q14/RIEG2] Rieger syndrome 2;
  • Gene: [13q14/TRANCE] TNF-related activation-induced cytokine; [OPGLG RANKL ]
  • Gene: [13q14/XRS] X-ray sensitivity;
  • Gene: [13q141/FKHR] forkhead (Drosophila) homolog 1 (rhabdomyosarcoma); rhabdomyosarcoma, type 2 (alveolar; MIM:268220); [RMSA RMS2 ]
  • Gene: [13q1411/CPB2] carboxypeptidase B2 (plasma); arginine carboxypeptidase (kininase 1); carboxypeptidase U; episodic angioedema (carboxypeptidase N? deficiency);
  • Gene: [13q1411/ESD] esterase D (EC:3.1.1.1); S-formylglutathione hydrolase (FGH; EC:3.1.2.12);
  • Gene: [13q142/P2RY5] purinergic receptor P2Y, G-protein coupled, 5 (purinoceptor P2Y5); G-protein coupled receptor, intron 17 of the retinoblastoma gene encoded;
  • Gene: [13q142/RB1] protein pp110 (retinoblastoma-associated); retinoblastoma 1; osteosarcoma (MIM:259500); [OSRC PP110 ]
  • Gene: [13q142/U16] orphan G protein coupled receptor U16;
  • Gene: [13q143/ATP7B] ATPase, Cu++ transporting, beta polypeptide (Wilson disease); Wilson disease (hepatolenticular degeneration);
  • Gene: [13q143/KPNA3] karyopherin (importin) alpha 3; [SRP4 ]
  • Gene: [13q143/LCP1] lymphocyte cytosolic protein 1 (64 kD); L-plastin; [LC64P CP64 ]
  • Gene: [13q143/TPT1] tumor protein, translationally controlled 1 (p23);
  • Gene: [13q2/POU4F1] POU domain, class 4, transcription factor 1; [BRN3A RDC1 ]
  • Gene: [13q21/FRA13B] fragile site 13q21, BrdU type, common;
  • Gene: [13q212/FRA13C] fragile site 13q21.2, aphidicolin type, common;
  • Gene: [13q22/BTF3L1] basic transcription factor 3, like 1 (lambda h27A);
  • Gene: [13q22/BTF3] basic transcription factor 3; [BTF3a BTF3b ]
  • Gene: [13q22/DDX9P] DEAD/H (Asp-Glu-Ala-Asp/His) box polypeptide 9 (RNA helicase A) pseudogene;
  • Gene: [13q22/EDNRB] endothelin receptor type B (non-specific); Waardenburg-Hirschsprung disease (MIM:277580); Hirschsprung disease 1 (HSCR1; recessive mutation; MIM:142623); Hirschsprung disease 2 (MIM:600155); [ETRB WS4 ]
  • Gene: [13q22/ERVT5] endogenous retroviral sequence, truncated 5 (band T9, 9.2 kb);
  • Gene: [13q3/LIG4] ligase IV, DNA, ATP-dependent;
  • Gene: [13q3/SLC15A1] solute carrier family 15 (oligopeptide transporter), member 1, intestinal; H+/peptide transporter 1 (intestinal); [PEPT1 ]
  • Gene: [13q3/TPP2] tripeptidyl peptidase II;
  • Gene: [13q32/DCT] dopachrome tautomerase (dopachrome delta-isomerase); tyrosinase-related protein 2;
  • Gene: [13q32/EEF1AL1] eukaryotic translation elongation factor 1 alpha-like 1;
  • Gene: [13q32/ERCC5] excision repair cross-complementing rodent repair deficiency, complementation group 5; xeroderma pigmentosum, complementation group G (MIM:278780); [ERCM2 UVDR ]
  • Gene: [13q32/FRA13D] fragile site 13q32, aphidicolin type, common;
  • Gene: [13q32/GPC5] glypican 5;
  • Gene: [13q32/GPR18] G protein-coupled receptor 18;
  • Gene: [13q32/PCCA] propionyl-CoA carboxylase, alpha polypeptide; glycinemia ketotic I (propionicacidemia I);
  • Gene: [13q32/PRKRI] protein-kinase, interferon-inducible double stranded RNA dependent inhibitor (p58);
  • Gene: [13q33/EFNB2] ephrin-B2; eph-related receptor tyrosine kinase ligand 5 (Htk ligand); [EPLG5 LERK5]
  • Gene: [13q33/SLC10A2] solute carrier family 10 (sodium/bile acid cotransporter family), member 2; sodium/taurocholate cotransporting polypeptide, ileal (NTCP2); bile acid malabsorption, primary; [NTCP2 ]
  • Gene: [13q34/ADPRTP1] poly(ADP-ribose) polymerase pseudogene 1; [PPOLP1 PADPRP ]
  • Gene: [13q34/ATP4B] ATPase, H+,K+ transporting, beta polypeptide;
  • Gene: [13q34/COL4A1] collagen, type IV, alpha 1;
  • Gene: [13q34/COL4A2] collagen, type IV, alpha 2;
  • Gene: [13q34/F10] coagulation factor X (thrombokinase, prothrombinase); Stuart-Prower disease (coagulation factor X deficiency);
  • Gene: [13q34/F7] coagulation factor VII (serum prothrombin conversion accelerator); hypoproconvertinemia (factor VII deficiency);
  • Gene: [13q34/FGF14] fibroblast growth factor 14; [FHF4 ]
  • Gene: [13q34/GAS6] growth arrest-specific 6; [AXLLG ]
  • Gene: [13q34/HHH] hyperornithinemia-hyperammonemia-homocitrullinemia syndrome; [HHHS ]
  • Gene: [13q34/LAMP1] lysosome-associated membrane protein 1 (LAMP-A; 120 kD); glycoprotein LAMP-1 (LAMP-A; lysosome-associated, membrane); [LAMPA ]
  • Gene: [13q34/RAP2A] RAS-related protein RAP-2A (K-rev); [RAP2 ]
  • Gene: [13q34/RHOK] rhodopsin kinase; G-protein-dependent receptor kinase 1; Oguchi disease (stationary nightblindness; MIM:258100);
  • Gene: [13q34/SOX1] SRY (sex determining region Y)-related HMG-box gene 1;
  • Gene: [13q34/STGD2] Stargardt disease 2 (autosomal dominant); macular dystrophy with flecks, type 2;
  • Gene: [13q34/TFDP1] transcription factor Dp-1 (E2F dimerization partner 1); [DP-1 ]
  • Gene: [13^/BCS1] breast cancer, ductal, suppressor 1; [BRCD1 BCDS1 ]
  • Gene: [13^/COX5BL6] cytochrome c oxidase subunit Vb-like 6;
  • Gene: [13^/ERR] ecotropic retroviral receptor;
  • Gene: [13^/FNTAL2] farnesyltransferase, CAAX box, alpha-like 2;
  • Gene: [13^/GPRK6P] G protein-coupled receptor kinase 6 pseudogene; [GPRK6L ]
  • Gene: [13^/IFNI56P] interferon-induced protein 56 pseudogene; [IFI56P G13P1 ]
  • Gene: [13^/LDHBL1] lactate dehydrogenase B-like 1;
  • Gene: [13^/STARP1] steroidogenic acute regulatory protein pseudogene 1;
  • Gene: [14p111/D14Z10] satellite DNA, alpha (probes pTRS-60/pTRS-63);
  • Gene: [14p111/D14Z1] satellite DNA, alpha, low copy (probe p82H);
  • Gene: [14p111/D14Z2] satellite DNA, alpha (clones: alphaT(1360)14-204; 14-12);
  • Gene: [14p111/D14Z3] satellite DNA, alpha (probe pTRS-47);
  • Gene: [14p111/D14Z4] satellite DNA, alpha (probe pTRA-1);
  • Gene: [14p111/D14Z5] satellite DNA, alpha (probe pTRA-4);
  • Gene: [14p111/D14Z6] satellite DNA, alpha (probe pTRA-2);
  • Gene: [14p111/D14Z7] satellite DNA, alpha (probes pTR9-H2/pTR9);
  • Gene: [14p111/D14Z8] satellite DNA, alpha (probe pTRA-7);
  • Gene: [14p111/D14Z9] satellite DNA, alpha (clone alpha-XT);
  • Gene: [14p12/D14FB2S1] satellite DNA, beta, NOR2-flanking subset 1; [DNFB2S1 ]

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