Gene: [02q/LCO] protooncogene LCO (liver cancer oncogene); hepatocellular carcinoma (HCC; protooncogene LCO); [LCA HCC ] — Gene: [03q13/HCLS1] hematopoietic cell-specific Lyn substrate 1; [HS1 ]


  • Gene: [02q/LCO] protooncogene LCO (liver cancer oncogene); hepatocellular carcinoma (HCC; protooncogene LCO); [LCA HCC ]
  • Gene: [02q/NCL] nucleolin;
  • Gene: [02q/NIDDM1] non-insulin-dependent diabetes mellitus (common, type 2) 1 (MIM:125853);
  • Gene: [02q/NPPC] natriuretic peptide precursor C;
  • Gene: [02q/RAB6] oncogene RAS-family, member rab6;
  • Gene: [02q/RNU20] RNA, U20 small nuclear;
  • Gene: [02q/SCN3A] sodium channel, voltage-gated, type III, alpha polypeptide;
  • Gene: [02q/SRMS] src-related kinase lacking C-terminal regulatory tyrosine and N-terminal myristylation sites;
  • Gene: [02q/TUBA1] tubulin, alpha 1 (testis specific); [TUBAT ]
  • Gene: [02q/VIS1] viral integration site 1 (oncogene HIS-1); [HIS-1 HS1 ]
  • Gene: [02q1/ATP6B1] ATPase, H+ transporting, lysosomal (vacuolar proton pump), beta polypeptide, 56/58kD, isoform 1 (kidney); vacuolar proton pump 3 (58kD subunit), isoform 1 (kidney);
  • Gene: [02q1/BUB1] budding uninhibited by benzimidazoles 1 (yeast homolog); mitotic checkpoint protein kinase BUB1; colorectal cancer with chromosomal instability;
  • Gene: [02q1/COX5B] cytochrome c oxidase subunit Vb;
  • Gene: [02q1/ED3] ectodermal dysplasia 3, anhidrotic; [ADHED ]
  • Gene: [02q1/GABRI] diazepam binding inhibitor; acyl-CoA binding protein; anxiety, pathologic (liability?); [DBI ACBP ]
  • Gene: [02q1/GLC1B] glaucoma 1, open angle, B (adult-onset); [POAG ]
  • Gene: [02q1/HTR5B] 5-hydroxytryptamine (serotonin) receptor 5B;
  • Gene: [02q1/IGKDEL] immunoglobulin kappa deleting element or like; [IGKDE ]
  • Gene: [02q1/IGO1] immunoglobulin orphon (transposed element) 1;
  • Gene: [02q1/INHBB] inhibin, beta B; activin, beta B;
  • Gene: [02q1/LAF4] lymphoid nuclear protein 4;
  • Gene: [02q1/MAL] mal, T-cell differentiation protein;
  • Gene: [02q1/PAX8] paired box homeotic gene 8;
  • Gene: [02q1/RALB] simian leukemia viral oncogene homolog B (ras related);
  • Gene: [02q1/RANBP2L1] RAN binding protein 2 like 1 (RANBP2-alpha);
  • Gene: [02q1/RANBP2] RAN binding protein 2; nucleoporin, 358kD; [NUP358 ]
  • Gene: [02q1/SLC20A1] solute carrier family 20 (phosphate transporter), member 1; gibbon ape leukemia virus receptor 1; [GLVR1 ]
  • Gene: [02q11/DUSP2] dual specificity phosphatase 2 (EC:3.1.3.48 and EC:3.1.3.16);
  • Gene: [02q11/SULT1C1] sulfotransferase family 1C1;
  • Gene: [02q112/FRA2A] fragile site 2q11.2, folic acid type, rare;
  • Gene: [02q112/RPL31] ribosomal protein L31;
  • Gene: [02q112/ST2H] growth stimulation-expressed gene (mouse) homolog; ST2 protein;
  • Gene: [02q12/IL1R1] interleukin 1 receptor, type I (alpha; antigen CDW121A); [IL1R IL1RA ]
  • Gene: [02q12/ZAP70] zeta-chain (TCR) associated protein kinase (70 kD); syk-related tyrosine kinase; protein tyrosine kinase ZAP-70 (zeta-associated protein, 70kD); selective T-cell defect;
  • Gene: [02q13/FRA2B] fragile site 2q13, folic acid type, rare;
  • Gene: [02q13/IL1A] interleukin 1, alpha (hematopoietin-1); rheumatoid arthritis, juvenile, association with; [IL1 ]
  • Gene: [02q13/IL1B] interleukin 1, beta;
  • Gene: [02q13/LIS2P1] lissencephaly sequence pseudogene; [LISP1 ]
  • Gene: [02q13/MALL] mal, T-cell differentiation protein-like;
  • Gene: [02q13/NPHP1] src homology 3 domain containing protein NPHP1; nephronophthisis 1 (juvenile); medullary cystic kidney disease (autosomal recessive);
  • Gene: [02q13/PROC] protein C (serine protease destroying coagulation factors Va and VIIIa); thrombophilia, hereditary (recurrent venous thrombosis, protein C deficiency);
  • Gene: [02q14/AMPHL] amphiphysin-like; box dependent MYC interacting protein 1 (BIN1); amphiphysin II; [BIN1 SH3P9 ]
  • Gene: [02q14/GLI2] chromatin-associated GLI-phosphoprotein 2; zinc finger oncoprotein GLI2; GLI-Kruppel family member GLI2;
  • Gene: [02q141/SCTR] secretin receptor;
  • Gene: [02q142/IL1RN] interleukin 1 receptor antagonist;
  • Gene: [02q2/ACVR1] activin A receptor, type I (65kD); activin A receptor, type II-like kinase 2;
  • Gene: [02q2/CACNB4] calcium channel, voltage-dependent, beta 4 subunit;
  • Gene: [02q2/GPR39] G protein-coupled receptor 39;
  • Gene: [02q2/GRB14] growth factor receptor-bound protein 14;
  • Gene: [02q2/NEM2] nemaline myopathy 2, autosomal recessive;
  • Gene: [02q2/NURR1] nuclear receptor related 1 (transcriptionally inducible); nuclear receptor of T cells (NOT); transcriptionally inducible nuclear receptor (TINUR); [NOT TINUR ]
  • Gene: [02q2/SCN6A] sodium channel, voltage-gated, type VI, alpha polypeptide;
  • Gene: [02q21/CHRNG] cholinergic receptor, nicotinic, gamma polypeptide (muscle); [ACHRG ]
  • Gene: [02q21/ERCC3] excision repair cross-complementing rodent repair deficiency, complementation group 3; basic transcription factor 2 (transcription factor TFIIH p89 polypeptide); xeroderma pigmentosum, complementation group B; trichothio
  • Gene: [02q21/LCT] lactase, intestinal (EC:3.2.1.108); phlorizin hydrolase (EC:3.2.1.62); disaccharide intolerance II (lactase deficiency); disaccharide intolerance III (adult lactase deficiency; MIM:223100);
  • Gene: [02q21/MCM6] minichromosome maintenance deficient (S. pombe) 6; DNA replication licensing factor MCM6;
  • Gene: [02q21/MGAT5] mannosyl (alpha-1,6-)-glycoprotein beta-1,6-N-acetylglucosaminyltransferase;
  • Gene: [02q21/NPY3R] neuropeptide Y receptor Y3-like receptor; G protein-coupled receptor LCR1 homolog; fusin (HIV-1 entry cofactor); leukocyte-derived seven-transmembrane domain receptor (LESTR); CXC chemokine receptor 4 (CXCR4); [NPYY3 LCR
  • Gene: [02q21/PHBP4] prohibitin pseudogene 4;
  • Gene: [02q21/POLR2D] RNA polymerase II (DNA directed) polypeptide D (16kD);
  • Gene: [02q213/FRA2F] fragile site 2q21.3, aphidicolin type, common;
  • Gene: [02q223/FRA2K] fragile site 2q22.3, folic acid type, rare;
  • Gene: [02q23/FAP] fibroblast activation protein, alpha;
  • Gene: [02q23/GCG] glucagon; hyperproglucagonemia (glucagon);
  • Gene: [02q23/SCN2A] sodium channel, voltage-gated, type II, alpha polypeptide (brain) (see also MIM:601219); [NAC2 HBSCII ]
  • Gene: [02q24/NEB] nebulin;
  • Gene: [02q24/PFIC2] progressive familial intrahepatic cholestasis 2;
  • Gene: [02q24/SCN1A] sodium channel, voltage-gated, type I, alpha polypeptide (brain); [SCN1 NAC1 ]
  • Gene: [02q241/GPD2] glycerol-3-phosphate dehydrogenase 2 (beta, mitochondrial); diabetes mellitus, type II;
  • Gene: [02q241/KCNJ3] potassium inwardly-rectifying channel, subfamily J, member 3;
  • Gene: [02q243/DPP4] dipeptidylpeptidase IV (antigen CD26); antigen CD26 (p250; monoclonal antibodies B1.19.2); adenosine deaminase complexing protein 2;
  • Gene: [02q3/ACADL] acyl-CoA dehydrogenase L (fatty acid long straight-chain C8 to C16); hypoglycemia, intermittent non-ketotic (LCAD deficiency); dicarboxylicaciduria (LCAD deficiency);
  • Gene: [02q3/ALS2] amyotrophic lateral sclerosis 2 (juvenile);
  • Gene: [02q3/CASP10] caspase 10, apoptosis-related cysteine protease;
  • Gene: [02q3/CHE2] cholinesterase 2 (serum; C5 band; pseudocholinesterase 2);
  • Gene: [02q3/CHGC] chromogranin C (secretogranin 2); [SCG2 ]
  • Gene: [02q3/CHN1] chimerin (chimaerin) 1 (alpha-chimerin, n-chimerin); [RhoGAP2 ]
  • Gene: [02q3/CHRND] cholinergic receptor, nicotinic, delta polypeptide (muscle); [ACHRD ]
  • Gene: [02q3/COL3A1] collagen, type III, alpha 1; Ehlers-Danlos syndrome, type IV (ecchymotic, Sack-Barabas type; autosomal dominant, MIM:130050); Ehlers-Danlos syndrome, type IV (ecchymotic, Sack-Barabas type; autosomal recessive, MIM:22535
  • Gene: [02q3/COL4A3] collagen, type IV, alpha 3 (Goodpasture antigen); Alport syndrome, autosomal recessive, type I (MIM:203780); Goodpasture syndrome (MIM:233450);
  • Gene: [02q3/COL4A4] collagen, type IV, alpha 4; Alport syndrome, autosomal recessive, type II (MIM:203780); hematuria, benign familial (141200);
  • Gene: [02q3/COL5A2] collagen, type V, alpha 2;
  • Gene: [02q3/CREB1] cAMP responsive element binding protein 1;
  • Gene: [02q3/CRYBA2] crystallin, beta A2 polypeptide;
  • Gene: [02q3/CRYGA] crystallin, gamma A polypeptide; [CRYG1 CRYG1P ]
  • Gene: [02q3/CRYGB] crystallin, gamma B polypeptide; [CRYG2 CRYG2P ]
  • Gene: [02q3/CRYGC] crystallin, gamma C polypeptide; [CRYG3 ]
  • Gene: [02q3/CRYGD] crystallin, gamma D polypeptide; cataract, Coppock-like; [CCL CRYG4 ]
  • Gene: [02q3/CRYGEP1] crystallin, gamma E pseudogene 1; [CRYG5 ]
  • Gene: [02q3/CRYGFP1] crystallin, gamma F pseudogene 1; [CRYG6 ]
  • Gene: [02q3/CRYGGP1] crystallin, gamma G pseudogene 1;
  • Gene: [02q3/CRYGP1] crystallin, gamma polypeptide pseudogene 1;
  • Gene: [02q3/CRYGP2] crystallin, gamma polypeptide pseudogene 2;
  • Gene: [02q3/CYP27A1] cytochrome P450, subfamily XXVIIA (steroid 27-hydroxylase), polypeptide 1; cerebrotendinous xanthomatosis (cerebral cholesterinosis; van Bogaert-Scherer-Epstein disease);
  • Gene: [02q3/E2F3P2] E2F transcription factor 3 pseudogene 2;
  • Gene: [02q3/FACL3] fatty-acid-CoA ligase, long-chain 3;
  • Gene: [02q3/FTHL3] ferritin, heavy polypeptide-like 3;
  • Gene: [02q3/FUCA1P] alpha-L-fucosidase 1 pseudogene;
  • Gene: [02q3/FZD5] frizzled (Drosophila) homolog 5;
  • Gene: [02q3/GBX2] gastrulation brain homeo box 2;
  • Gene: [02q3/GLS] glutaminase (phosphate-activated);
  • Gene: [02q3/GPC1] glypican 1;
  • Gene: [02q3/HTR2B] 5-hydroxytryptamine (serotonin) receptor 2B;
  • Gene: [02q3/ICR2B] ichthyosis congenita IIB (lamellar ichthyosis, type 2); [LI2 ]
  • Gene: [02q3/IGFB2] insulin-like growth factor binding protein 2 (36kD); [IBP2 IGFBP2 ]
  • Gene: [02q3/IHH] Indian hedgehog (Drosophila) homolog;
  • Gene: [02q3/INHA] inhibin, alpha; activin, alpha;
  • Gene: [02q3/INPP5D] inositol polyphosphate-5-phosphatase, type IV, 145kD;
  • Gene: [02q3/ITGA4] integrin, alpha 4 (antigen CD49D; alpha 4 subunit of VLA-4 receptor); very late activation protein-4 receptor (MIM:192972); [CD49D VLA4 ]
  • Gene: [02q3/ITGAV] integrin, alpha V (antigen CD51); vitronectin receptor, alpha polypeptide; [CD51 VNRA ]
  • Gene: [02q3/LRP2] low density lipoprotein receptor-related protein 2 (glycoprotein 330; megalin);
  • Gene: [02q3/MYL1] myosin, light polypeptide 1, alkali; skeletal, fast; [MLC1F HSLC1 ]
  • Gene: [02q3/NDUFS1] NADH dehydrogenase (ubiquinone) Fe-S protein 1 (75kD; NADH-CoQ reductase; EC:1.6.5.3, EC:1.6.99.3);
  • Gene: [02q3/PI7] protease inhibitor 7 (protease nexin I); [PNI ]
  • Gene: [02q3/PMS1] postmeiotic segregation increased (S. cerevisiae) 1 (mismatch repair gene); hereditary nonpolyposis colon cancer (HNPCC); [PMSL1 ]
  • Gene: [02q3/PNKD] paroxysmal nonkinesiogenic dyskinesia; choreoathetosis, familial paroxysmal (Mount-Reback syndrome); dystonia 8; [FPD1 PDC ]
  • Gene: [02q3/PPH1] primary pulmonary hypertension 1; [PPH ]
  • Gene: [02q3/PTPRN] protein tyrosine phosphatase, receptor type, N; islet cell antigen 512 (IA-2); islet cell autoantigen 3 (ICA512);
  • Gene: [02q3/RPE] ribulose-5-phosphate-3-epimerase;
  • Gene: [02q3/RPL37A] ribosomal protein L37a;
  • Gene: [02q3/SCYA20] small inducible cytokine subfamily A (Cys-Cys), member 20; beta-chemokine Exodus; macrophage inflammatory protein 3 alpha (MIP-3-alpha); liver and activation-regulated chemokine (LARC); [MIP3A LARC ]
  • Gene: [02q3/TNS] tensin;
  • Gene: [02q3/UBL1] ubiquitin-like 1, 12kD; sentrin; ubiquitin-like protein SMT3C; [SMTH3 SMT3C ]
  • Gene: [02q3/VGL] vigilin;
  • Gene: [02q3/ZNF142] zinc finger protein 142 (clone pHZ-49); [KIAA0236 ]
  • Gene: [02q31/FRA2G] fragile site 2q31, aphidicolin type, common;
  • Gene: [02q31/GAD1] glutamate decarboxilase 1 (brain, 67kD); pyridoxine dependency with seizures (GAD deficiency);
  • Gene: [02q31/HOXD10] homeo box D10(4D), homologous to mouse Hox-4.4; [HOX4D ]
  • Gene: [02q31/HOXD11] homeo box D11(4F), homologous to mouse Hox-4.6; [HOX4F ]
  • Gene: [02q31/HOXD12] homeo box D12(4H), homologous to mouse Hox-4.8; [HOX5 HOX4H ]
  • Gene: [02q31/HOXD13] homeo box D13(4I), homologous to mouse Hox-4.9; synpolydactyly (syndactyly type II; MIM:186000); [HOX5 HOX4I ]
  • Gene: [02q31/HOXD1] homeo box D1(4G), homologous to mouse Hox-4.7; [HOX4G ]
  • Gene: [02q31/HOXD3] homeo box D3(4A), homologous to mouse Hox-4.1; [HOX4 HOX4A ]
  • Gene: [02q31/HOXD4] homeo box D4(4B), homologous to mouse Hox-4.2; [HOX4B HOX5 ]
  • Gene: [02q31/HOXD8] homeo box D8(4E), homologous to mouse Hox-4.5; [HOX4E ]
  • Gene: [02q31/HOXD9] homeo box D9(4C), homologous to mouse Hox-4.3; [HOX4C ]
  • Gene: [02q31/IDDM7] insulin-dependent diabetes mellitus 7;
  • Gene: [02q31/IL17] interleukin 17; cytotoxic T-lymphocyte-associated serine esterase 8;
  • Gene: [02q31/NFE2L2] nuclear factor, erythroid-derived 2-like 2; [NRF2 ]
  • Gene: [02q31/SP3] Sp3 transcription factor;
  • Gene: [02q31/TMD] tibial muscular dystrophy, tardive;
  • Gene: [02q31/TTN] titin;
  • Gene: [02q32/ARVD4] arrhythmogenic right ventricular dysplasia 4;
  • Gene: [02q32/ATF4] activating transcription factor 4; tax-responsive enhancer element B67; [TXREB ]
  • Gene: [02q32/CHRNA1] cholinergic receptor, nicotinic, alpha polypeptide 1 (muscle); [CHRNA ACHRA ]
  • Gene: [02q32/CREB2] cAMP responsive element binding protein 2; activating transcription factor 2; [ATF2 TREB7 ]
  • Gene: [02q32/DLX1] distal-less homeo box 1;
  • Gene: [02q32/DLX2] distal-less homeo box 2;
  • Gene: [02q32/INPP1] inositol polyphosphate-1-phosphatase;
  • Gene: [02q32/NEUROD1] neurogenic differentiation 1;
  • Gene: [02q32/TFPI] tissue factor pathway inhibitor; lipoprotein-associated coagulation inhibitor; [LACI ]
  • Gene: [02q321/FRA2H] fragile site 2q32.1, aphidicolin type, common;
  • Gene: [02q321/GDF8] growth differentiation factor 8 (myostatin); [MSTN ]
  • Gene: [02q33/AOX1] aldehyde oxidase 1; molybdenum cofactor deficiency, type A;
  • Gene: [02q33/CD28] antigen CD28 (Tp44; T-cell-specific);
  • Gene: [02q33/CLK1] CDC-like kinase 1;
  • Gene: [02q33/CTLA4] cytotoxic T-lymphocyte-associated serine esterase 4; T cell/natural killer cells serine esterase 4;
  • Gene: [02q33/FRA2I] fragile site 2q33, aphidicolin type, common;
  • Gene: [02q33/FZD7] frizzled (Drosophila) homolog 7; [FzE3 ]
  • Gene: [02q33/IDDM12] insulin-dependent diabetes mellitus 12;
  • Gene: [02q33/ORC2L] origin recognition complex, subunit 2 (yeast homolog)-like; origin of replication 2 (Saccharomyes) homolog-like;
  • Gene: [02q33/PLCE] phospholipase C, epsilon (lung carcinoma-related); lung carcinoma?;
  • Gene: [02q33/PTHR2] parathyroid hormone receptor 2; [PTHR2R ]
  • Gene: [02q333/IDH1] isocitrate dehydrogenase 1 (NADP+), soluble;
  • Gene: [02q34/EGFR4] avian erythroblastic leukemia viral (v-erb-b2) oncogene homolog 4; oncogene homolog ERBB4; protein tyrosine kinase, receptor ERBB4;
  • Gene: [02q34/FN1] fibronectin 1 (dysfibronectinemic Ehlers-Danlos syndrome X); Ehlers-Danlos syndrome, type X (dysfibronectinemic; MIM:225310);
  • Gene: [02q34/IDDM13] insulin-dependent diabetes mellitus 13;
  • Gene: [02q34/MAP2] microtubule-associated protein 2 (280kD; dendrite-specific); [MTB ]
  • Gene: [02q34/TNP1] transition protein 1 (during histone to protamine replacement);
  • Gene: [02q35/CPS1] carbamoyl phosphate synthetase 1, mitochondrial; hyperammonemia II (due to carbamoyl phosphate synthetase 1 deficiency);
  • Gene: [02q35/DES] desmin (skeletin; intermediate filament, muscle type); distal myopathy with cardiomyopathy;
  • Gene: [02q35/IL8RA] interleukin 8 receptor, alpha (high affinity; antigen CDW128); chemokine (C-X-C) receptor 1; [CMKAR1 CXCR1 ]
  • Gene: [02q35/IL8RBP] interleukin 8 receptor, beta (high affinity) pseudogene;
  • Gene: [02q35/IL8RB] interleukin 8 receptor, beta (high affinity);
  • Gene: [02q35/NRAMP1] natural resistance-associated macrophage protein 1 (might include Leishmaniasis); [LSH NRAMP ]
  • Gene: [02q35/PSMB3] proteasome (prosome, macropain) subunit, beta type, 3 (homolog of yeast PUP3); [HC10-II ]
  • Gene: [02q35/VIL1] villin 1;
  • Gene: [02q35/XRCC5] X-ray repair complementing defective repair in Chinese hamster cells 5; thyroid autoantigen, 80kD (antigen Ku; p80; lupus antigen); ATP-dependent DNA helicase II, 86kD;
  • Gene: [02q36/IRS1] insulin receptor substrate 1; noninsulin-dependent diabetes mellitus (NIDDM, MIM:125853); [HIRS-1 ]
  • Gene: [02q36/PAX3] paired box homeotic gene 3; Waardenburg syndrome, type 1; Waardenburg syndrome, type 3 (with upper limb anomalies; Klein-Waardenburg syndrome; MIM:148820); rhabdomyosarcoma, type 2 (alveolar; MIM:268220); craniofacial-dea
  • Gene: [02q36/PDE6D] phosphodiesterase 6D, cGMP-specific, rod, delta (17kD);
  • Gene: [02q36/SLC4A3] solute carrier family 4, anion exchanger, member 3 (neuronal and cardiac); [AE3 SLC2C ]
  • Gene: [02q37/ALPIF] alkaline phosphatase, intestinal, fetal (Kasahara isozyme);
  • Gene: [02q37/ALPT] alkaline phosphatase, testicular/T-cell (placental-like 2); alkaline phosphatase, placental-like (Nagao isozyme); alkaline phosphatase, placental-like 2;
  • Gene: [02q37/BDMR] brachydactyly-mental retardation syndrome; Albright hereditary osteodystrophy, type 3; brachydactyly, type E (MIM:113300);
  • Gene: [02q37/HDLBP] high density lipoprotein binding protein;
  • Gene: [02q37/NEDD5] neural precursor cell expressed, developmentally down-regulated 5; differentiation 6; deoxyguanosine triphosphate triphosphohydrolase (deoxy-GTPase);
  • Gene: [02q37/PSMD1] proteasome (prosome, macropain) 26S subunit, non-ATPase, 1 (homolog of yeast SEN3); [S1 P112 ]
  • Gene: [02q37/SPP2] secreted phosphoprotein 2, 24kD; [spp24 ]
  • Gene: [02q37/UGT1] UDP-glucuronosyltransferase 1; Crigler-Najjar syndrome type I (MIM:218800); Crigler-Najjar syndrome type II (Gilbert syndrome; MIM:143500);
  • Gene: [02q371/ALPIA] alkaline phosphatase, intestinal, adult;
  • Gene: [02q371/ALPPR] alkaline phosphatase, placental (Regan isozyme);
  • Gene: [02q371/SAG] S-antigen (retinal and pineal protein 45 kD; arrestin S); arrestin S (S-antigen); Oguchi disease (stationary nightblindness; MIM:258100);
  • Gene: [02q373/AGXT] alanine-glyoxylate aminotransferase (EC:2.6.1.44; hyperoxaluria I); serine-pyruvate aminotransferase (EC:2.6.1.51); oxalosis I (hyperoxaluria I; glycolicaciduria);
  • Gene: [02q373/COL6A3] collagen, type VI, alpha 3; Bethlem myopathy;
  • Gene: [02q373/FRA2J] fragile site 2q37.3, aphidicolin type, common;
  • Gene: [02q373/GPR35] G protein-coupled receptor 35;
  • Gene: [02q373/PDCD1] programmed cell death 1;
  • Gene: [02q373/PPP1R7] protein phosphatase 1, regulatory (inhibitor) subunit 7;
  • Gene: [02^/ACHM2] achromatopsia (rod monochromacy) 2; rod monochromacy (RMCH; total colorblindness); [RMCH ]
  • Gene: [02^/ACTL3] actin-like sequence 3;
  • Gene: [02^/ADRA2B] adrenergic, alpha-2B-, receptor; [ADRA2RL1 ]
  • Gene: [02^/ATP5BL1] ATP synthase, H+ transporting, mitochondrial F1 complex, beta polypeptide-like 1; [ATPMBL1 ]
  • Gene: [02^/ATP5G3] ATP synthase, H+ transporting, mitochondrial F0 complex, subunit c (subunit 9), isoform 3;
  • Gene: [02^/CYP1ARA] aryl hydrocarbon hydroxylase inducibility; bronchogenic cancer (liability?); [AHHR AHHI ]
  • Gene: [02^/DTYMK] deoxythymidylate kinase;
  • Gene: [02^/EEF1B2] eukaryotic translation elongation factor 1 beta 2;
  • Gene: [02^/HNMT] histamine N-methyltransferase;
  • Gene: [02^/HPCAL1] hippocalcin-like peptide 1;
  • Gene: [02^/HVBS4] hepatitis B virus integration site 4;
  • Gene: [02^/IFNB5] interferon, beta 5, fibroblast;
  • Gene: [02^/INSL1] insulin-like 1;
  • Gene: [02^/ITGA6] integrin, alpha 6; epidermolysis bullosa, junctional;
  • Gene: [02^/ITGB6] integrin, beta 6;
  • Gene: [02^/LDHAL3] lactate dehydrogenase A-like 3;
  • Gene: [02^/LTBP1] latent transforming growth factor beta binding protein 1;
  • Gene: [02^/MIC18] antigen MIC18 (monoclonal antibody AUA1);
  • Gene: [02^/MSK8] antigen MSK8 (monoclonal antibody L230);
  • Gene: [02^/NEFLL1] neurofilament, light polypeptide-like 1;
  • Gene: [02^/NPAS2] neuronal PAS domain protein 2; [MOP4 ]
  • Gene: [02^/PCH1] protein spot in 2-D gels (MM 250 kD; pI 7.0);
  • Gene: [02^/PLGL] plasminogen-like;
  • Gene: [02^/PTMA] prothymosin, alpha (gene sequence 28); [TMSA ]
  • Gene: [02^/RACH] acetylcholinesterase derepressor; [ACEE ]
  • Gene: [02^/RAD52P] RAD52 pseudogene;
  • Gene: [02^/SLC9A2] solute carrier family 9 (sodium/hydrogen exchanger), isoform 2; [NHE2 ]
  • Gene: [02^/SLC9A4] solute carrier family 9 (sodium/hydrogen exchanger), isoform 4; [NHE4 ]
  • Gene: [02^/TACR1] tachykinin receptor 1 (substance P receptor, neurokinin 1 receptor); [NK1R ]
  • Gene: [02^/TMSL2] thymosin-like 2;
  • Gene: [02^/TNFAI6] tumor necrosis factor, alpha-induced protein 6; [TNFAIP6 ]
  • Gene: [02^/TSE2] tissue specific extinguisher 2;
  • Gene: [02^/UCN] urocortin; [UROC ]
  • Gene: [02^/UGP2] UDP-glucose pyrophosphorylase 2;
  • Gene: [02^/ZNF2] zinc finger protein 2 (A1-5);
  • Gene: [03p/BBS3] Bardet-Biedl syndrome 3;
  • Gene: [03p/DFNB6] deafness, autosomal recessive 6; [NSRD6 ]
  • Gene: [03p/DNASE1L3] deoxyribonuclease I-like 3;
  • Gene: [03p/ITIH4] inter-alpha (globulin) inhibitor, H polypeptide-like 1; inter-alpha (globulin) inhibitor H4; inter-alpha-trypsin inhibitor, heavy chain-related protein; plasma kallikrein-sensitive glycoprotein; [IHRP PK120 ]
  • Gene: [03p/LRS1] Larsen syndrome 1 (autosomal dominant);
  • Gene: [03p/MSK10] antigen MSK10 (monoclonal antibody AJ425);
  • Gene: [03p/MSK32] antigen MSK32 (monoclonal antibody K66);
  • Gene: [03p/MSK33] antigen MSK33 (monoclonal antibody SR3);
  • Gene: [03p/MSK9] antigen MSK9 (monoclonal antibody K15);
  • Gene: [03p/PEO2] progressive external ophthalmoplegia, type 2;
  • Gene: [03p/SCA7] spinocerebellar ataxia 7 (olivopontocerebellar atrophy with retinal degeneration);
  • Gene: [03p/SEX2] transmembrane protein SEP;
  • Gene: [03p/TMF1] TATA element modulatory factor 1 (123kD);
  • Gene: [03p/TNNC1] troponin C1, cardiac and skeletal, slow; [TNCC TNC ]
  • Gene: [03p/WNT5A] wingless-type MMTV integration site 5A, human homolog;
  • Gene: [03p1/HTR1F] 5-hydroxytryptamine (serotonin) receptor 1F;
  • Gene: [03p1/MITF] microphthalmia-associated transcription factor; Waardenburg syndrome, type 2A (WS2A; MIM:193510); [WS2A ]
  • Gene: [03p1/RPL24] ribosomal protein L24;
  • Gene: [03p11/POU1F1] POU domain, class 1, transcription factor 1; pituitary-specific transcription factor 1; growth hormone factor 1; combined pituitary hormone deficiency; [PIT1 GHF1]
  • Gene: [03p112/EPHA3] ephrin receptor EphA3; eph-like tyrosine kinase 1; human embryo kinase 1;
  • Gene: [03p12/ALDRP] aldehyde reductase (aldose reductase) pseudogene;
  • Gene: [03p142/FHIT] fragile histidine triad gene;
  • Gene: [03p142/FRA3B] fragile site 3p14.2, aphidicolin type, common;
  • Gene: [03p142/PTPRG] protein tyrosine phosphatase, receptor type, gamma polypeptide;
  • Gene: [03p142/RCA1] renal cell carcinoma, familial, associated 1; [HRCA1 RCC1 ]
  • Gene: [03p143/ACOX2] acyl-CoA oxidase, branched-chain, peroxisomal;
  • Gene: [03p143/TKT1] transketolase 1; Wernicke-Korsakoff syndrome;
  • Gene: [03p2/ACAA] acetyl-CoA acyltransferase (beta-ketothiolase); peroxisomal 3-oxoacyl-CoA thiolase; pseudo-Zellweger syndrome;
  • Gene: [03p2/ACVR2B] activin A receptor, type IIB (85kD);
  • Gene: [03p2/ATP2B2] ATPase, Ca++ transporting, plasma membrane 2;
  • Gene: [03p2/CCK] cholecystokinin;
  • Gene: [03p2/CMD1E] cardiomyopathy, dilated 1E (autosomal dominant); cardiomyopathy, dilated 2A (autosomal recessive); [CMD2A DCM ]
  • Gene: [03p2/COLQ] collagen-like tail subunit (single strand of homotrimer) of asymmetric acetylcholinesterase;
  • Gene: [03p2/FBLN2] fibulin 2;
  • Gene: [03p2/FECHP] ferrochelatase pseudogene;
  • Gene: [03p2/GOLGA4] Golgi autoantigen, golgin subfamily a, 4 (golgin-245, p230); [GOLG GCP2 ]
  • Gene: [03p2/GPR28] G protein-coupled receptor 28;
  • Gene: [03p2/IL5RA] interleukin 5 receptor, alpha (antigen CD125); [IL5R ]
  • Gene: [03p2/ITPR1] inositol 1,4,5-triphosphate receptor, type 1;
  • Gene: [03p2/MFS2] Marfan syndrome 2;
  • Gene: [03p2/MOBP] myelin-associated oligodendrocyte basic protein;
  • Gene: [03p2/MYD88] myeloid differentiation primary response gene (MYD88);
  • Gene: [03p2/NKTR] natural killer-tumor recognition sequence;
  • Gene: [03p2/OXTR] oxytocin receptor;
  • Gene: [03p2/PLCD1] phospholipase C, delta 1;
  • Gene: [03p2/RAB5A] oncogene RAS-family, member rab5A; [RAB5 ]
  • Gene: [03p2/RPL15] ribosomal protein L15 (L10);
  • Gene: [03p2/SCLC] small cell lung cancer; [SCCL SCLC1 ]
  • Gene: [03p2/SEC13L1] SEC13 (S. cerevisiae)-like 1; [SEC13R ]
  • Gene: [03p2/SLC6A1] solute carrier family 6 (neurotransmitter transporter, GABA), member 1; [GABT1 ]
  • Gene: [03p2/SLC6A6] solute carrier family 6 (neurotransmitter transporter, taurine), member 6; [TAUT ]
  • Gene: [03p2/STAC] src homology three (SH3) and cysteine rich domain;
  • Gene: [03p2/TCEA1] transcription elongation factor A (SII), 1; [GTF2S SII ]
  • Gene: [03p2/TGM4] transglutaminase 4 (prostate); protein-glutamine-gamma-glutamyltransferase (transglutaminase 4);
  • Gene: [03p2/TNA] tetranectin (plasminogen-binding protein);
  • Gene: [03p2/VHL] von Hippel-Lindau gene; von Hippel-Lindau syndrome; renal cell carcinoma (adenocarcinoma of kidney); [RCC RCC1 ]
  • Gene: [03p2/ZNF166] zinc finger protein 166;
  • Gene: [03p2/ZNF167] zinc finger protein 167;
  • Gene: [03p2/ZNF168] zinc finger protein 168;
  • Gene: [03p2/ZNF35P] zinc finger protein 35 (clone HF.10) pseudogene;
  • Gene: [03p21/APEH] N-acylaminoacyl-peptide hydrolase;
  • Gene: [03p21/ARF2] ADP-ribosylation factor 2;
  • Gene: [03p21/BAP1] BRCA1 associated protein-1; ubiquitin carboxy-terminal hydrolase;
  • Gene: [03p21/CACNA1D] calcium channel, voltage-dependent, L type, alpha 1D subunit; calcium channel, L type, alpha 1 polypeptide, isoform 2 (neuroendocrine); [CACNL1A2 ]
  • Gene: [03p21/CDC25A] cell division cycle 25A; protein tyrosine phosphatase CDC25A;
  • Gene: [03p21/CMKBR1] chemokine (C-C) receptor 1; [CC-CKR-1 ]
  • Gene: [03p21/CMKBR2] chemokine (C-C) receptor 2; [CC-CKR-2 ccr2 ]
  • Gene: [03p21/CMKBR5] chemokine (C-C) receptor 5; [CC-CKR-5 ccr5 ]
  • Gene: [03p21/CMKBR8] chemokine (C-C) receptor 8; G protein-coupled receptor GPR-CY6; [CMKBRL2 ]
  • Gene: [03p21/DAG1] dystroglycan 1 (dystrophin-associated glycoprotein 1, 43kD/156kD);
  • Gene: [03p21/DUSP7] dual specificity phosphatase 7 (EC:3.1.3.48 and EC:3.1.3.16);
  • Gene: [03p21/GCST] glycine cleavage system protein T; aminomethyltransferase; tetrahydrofolate aminomethyltransferase; hyperglycinemia, isolated nonketotic, type II;
  • Gene: [03p21/GNAI2] guanine nucleotide binding protein (G protein), alpha inhibiting activity polypeptide 2; adenylate cyclase inhibitor GI, alpha-I2 (GIP2 oncogene); adrenal cortical tumor (granulosa cell tumor; thecoma); pituitary adenoma
  • Gene: [03p21/GNAT1] guanine nucleotide binding protein (G protein), alpha transducing activity polypeptide 1; adenylate cyclase transductor GT, alpha-T1;
  • Gene: [03p21/GPR13] G protein-coupled receptor 13; chemokine (C-X3-C) receptor 1 (MIM:602237); chemokine (C-C) receptor-like 1; fractalkine receptor CX3CR1 (MIM:602237); [V28 CX3CR1 ]
  • Gene: [03p21/GPR5] G protein-coupled receptor 5;
  • Gene: [03p21/HAUSP] herpes virus-associated ubiquitin-specific protease; VMW110-associated 135-kD protein;
  • Gene: [03p21/IMPDH2] IMP (inosine monophosphate) dehydrogenase 2;
  • Gene: [03p21/ITIH1] inter-alpha-trypsin inhibitor, H1 polypeptide (of protein HC); [IATIH ]
  • Gene: [03p21/ITIH3] inter-alpha-trypsin inhibitor, H3 polypeptide (of protein HC);
  • Gene: [03p21/LAMB2] laminin, beta 2 (laminin S; synapses); [LAMS ]
  • Gene: [03p21/LTF] lactotransferrin;
  • Gene: [03p21/MAP4] microtubule-associated protein 4 (210kD);
  • Gene: [03p21/MYL3] myosin, light polypeptide 3, alkali; ventricular, skeletal, slow; [MLC1V/Sb ]
  • Gene: [03p21/PPP2R5C] protein phosphatase 2, regulatory subunit B (B56), gamma isoform;
  • Gene: [03p21/PTHR1] parathyroid hormone receptor; metaphyseal chondrodysplasia, Murk Jansen type (MIM:156400);
  • Gene: [03p21/SCN5A] sodium channel, voltage-gated, type V, alpha polypeptide; long (electrocardiographic) QT syndrome 3; idiopathic ventricular fibrillation; [LQT3 IVF ]
  • Gene: [03p21/SMARCC1] SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily c, member 1; chromatin remodeling complex, BRG1-associated factor, 155kD; [SRG3 BAF155 ]
  • Gene: [03p21/TCTA] T-cell leukemia translocation altered gene;
  • Gene: [03p21/TDGF1] teratocarcinoma-derived growth factor 1 (CRIPTO growth factor); [CRGF ]
  • Gene: [03p21/UBE1L] ubiquitin-activating enzyme E1 homolog;
  • Gene: [03p21/UQCRC1] ubiquinol-cytochrome c reductase core protein 1;
  • Gene: [03p21/ZNF35] zinc finger protein 35 (clone HF.10); [HF10 ]
  • Gene: [03p211/ACY1] aminoacylase 1;
  • Gene: [03p211/ALAS1] delta-aminolevulinate synthase 1 (housekeeping);
  • Gene: [03p211/STK2] serine/threonine kinase 2;
  • Gene: [03p213/ARHA] protooncogene ARH-12 (RHOA; Aplysia ras-related homolog 12); [rhoH12 ARH12 ]
  • Gene: [03p213/CAMP] cathelicidin antimicrobial peptide; peptide antibiotic, PR-39 (porcine) homolog; cationic antimicrobial protein (18kD); [FALL39 ]
  • Gene: [03p213/CD39L3] CD39-like 3;
  • Gene: [03p213/CISH] cytokine inducible SH2-containing protein; [CIS ]
  • Gene: [03p213/CMKBR3] chemokine (C-C) receptor 3; [CC-CKR-3 ]
  • Gene: [03p213/CMKBR9] chemokine (C-C) receptor 9; [CCR9 CCR10 D6 ]
  • Gene: [03p213/COL7A1] collagen, type VII, alpha 1 (long-chain); epidermolysis bullosa, dystrophic (Pasini type; MIM:131750); epidermolysis bullosa (Cockayne-Touraine type; 131800); epidermolysis bullosa, pretibial (MIM:131850); epidermolysi
  • Gene: [03p213/CTNNB1] catenin (cadherin-associated protein), beta 1 (88kD);
  • Gene: [03p213/GPX1] glutathione peroxidase 1 (cellular); hemolytic anemia (glutathione peroxidase 1 deficiency);
  • Gene: [03p213/ITGA4L] integrin, alpha 4-like;
  • Gene: [03p213/LAMR1] laminin receptor 1 (67kD); colon carcinoma laminin-binding protein; 40S ribosomal protein P40; [LAMBR ]
  • Gene: [03p213/MAPKAP3] mitogen-activated protein kinase-activated protein kinase 3;
  • Gene: [03p213/MLH1] mutL (E. coli) homolog 1; colon cancer, nonpolyposis type 2; [COCA2 ]
  • Gene: [03p213/MST1R] macrophage stimulating 1 receptor; tyrosine kinase, c-met-related;
  • Gene: [03p213/MST1] macrophage stimulating 1 (hepatocyte growth factor-like); [HGFL ]
  • Gene: [03p213/SEMA3F] semaphorin IIIF;
  • Gene: [03p213/SEMA4] semaphorin IV;
  • Gene: [03p213/SEMA5A] semaphorin VA; [LUCA-1 ]
  • Gene: [03p213/UNP] ubiquitin specific protease, proto-oncogene;
  • Gene: [03p213/ZNF52] zinc finger protein 52;
  • Gene: [03p213/ZNF64] zinc finger protein 64;
  • Gene: [03p2131/CACT] carnitine-acylcarnitine translocase; carnitine-acylcarnitine translocase deficiency;
  • Gene: [03p2133/GLB1] galactosidase, beta 1, acid; gangliosidosis, generalized GM1, type I, infant (galactosidase-beta-1 deficiency); gangliosidosis, generalized GM1, type II, juvenile (galactosidase-beta-1 deficiency; MIM:230600); gangliosi
  • Gene: [03p22/TGFBR2] transforming growth factor, beta receptor II (70-80kD);
  • Gene: [03p22/VIPR1] vasoactive intestinal peptide receptor 1; adenylate cyclase activating polypeptide 1 (pituitary) receptor type 2; [VIPR RDC1 ]
  • Gene: [03p23/SATB1] special AT-rich sequence binding protein 1 (binds to nuclear matrix/scaffold-associating DNA's);
  • Gene: [03p24/CAF] CREBBP-associated factor;
  • Gene: [03p24/CMKBR4] chemokine (C-C) receptor 4; [CC-CKR-4 ]
  • Gene: [03p24/DAZLA] deleted in azoospermia-like, autosomal; [DAZH SPGYLA ]
  • Gene: [03p24/RARB] retinoic acid receptor, beta; HBV-activated protein; [HAP ]
  • Gene: [03p24/TOP2B] topoisomerase (DNA) II beta (180kD);
  • Gene: [03p242/FRA3A] fragile site 3p24.2, aphidicolin type, common;
  • Gene: [03p242/UBE2E2] ubiquitin-conjugating enzyme E2E 2 (homologous to yeast UBC4/5);
  • Gene: [03p25/BTD] biotinidase; multiple carboxylase deficiency, late onset;
  • Gene: [03p25/CAV3] caveolin 3 (M-caveolin); muscular dystrophy, limb-girdle, type IC; [LGMD1C VIP-21 ]
  • Gene: [03p25/FANCD] Fanconi anemia, complementation group D gene; Fanconi anemia, complementation group D; Fanconi pancytopenia, type 4; [FACD FAD ]
  • Gene: [03p25/HRH1] histamine receptor H1;
  • Gene: [03p25/OGG1] 8-oxoguanine DNA glycosylase;
  • Gene: [03p25/PPARG] peroxisome proliferative activated receptor, gamma;
  • Gene: [03p25/RAF1] murine leukemia viral homologue 1 (protooncogene RAF-1); [MIL ]
  • Gene: [03p25/TR4] TR4 nuclear hormone receptor; orphan receptor TR4; [TAK1 ]
  • Gene: [03p25/WNT7A] wingless-type MMTV integration site 7A, human homolog;
  • Gene: [03p251/RAD23B] RAD23 (S. cerevisiae) homolog B; [HHR23B ]
  • Gene: [03p251/XPC] xeroderma pigmentosum, complementation group C;
  • Gene: [03q/ADCY5] adenylate cyclase 5;
  • Gene: [03q/ASSP7] argininosuccinate synthetase pseudogene 7;
  • Gene: [03q/CASR] calcium-sensing receptor; hypocalciuric hypercalcemia 1 (HHC1; MIM:145980); severe neonatal hyperparathyroidism (MIM:239200); hypocalcemia, autosomal dominant (MIM:601198); hyperparathyroidism, familial isolated (FIH; MIM:1
  • Gene: [03q/CBLB] Cas-Br-M (murine) ectropic retroviral transforming sequence b;
  • Gene: [03q/CMT2B] Charcot-Marie-Tooth neuropathy 2B;
  • Gene: [03q/MYLK] myosin, light polypeptide kinase;
  • Gene: [03q/PCYT1] phosphate cytidylyltransferase 1, choline;
  • Gene: [03q/PNIA5] protein spot in 2-D gels (77kD; pI 5.0);
  • Gene: [03q/TERC] telomerase RNA component; [hTR ]
  • Gene: [03q/UPK1B] uroplakin 1B (tetraspan);
  • Gene: [03q/ZNF9] zinc finger protein 9; [CNBP ]
  • Gene: [03q1/COL8A1] collagen, type VIII, alpha 1 (endothelial);
  • Gene: [03q1/GPR15] G protein-coupled receptor 15;
  • Gene: [03q1/TFG] TRK-fused gene (TRKT3 oncogene); [TRKT3 ]
  • Gene: [03q12/GBE1] glucan (1,4-alpha-), branching enzyme 1 (glycogen branching enzyme); Andersen disease, glycogen storage disease type IV;
  • Gene: [03q13/ALCAM] activated leukocyte-cell adhesion molecule (CD6 ligand);
  • Gene: [03q13/CD47] antigen CD47 (Rh-related antigen, integrin-associated signal transducer); integrin-associated signal transducer (CD47); antigen identified by monoclonal antibody 1D8 (MER6); integrin-associated protein (IAP; CD47 glycopro
  • Gene: [03q13/CSTA] cystatin A (cystatin AS; stefin A); [STF1 ]
  • Gene: [03q13/ETM1] tremor, familiar essential, 1; [ETM FET1 ]
  • Gene: [03q13/FACL1] fatty-acid-CoA ligase, long-chain 1; palmitoyl-CoA ligase 1;
  • Gene: [03q13/GAP43] neuron growth-associated protein 43 kD; protein GAP43, neuron growth-associated; [p57 PP46 B-50]
  • Gene: [03q13/HCLS1] hematopoietic cell-specific Lyn substrate 1; [HS1 ]