Gene: [07q112/CD36] antigen CD36 (collagen type I receptor, thrombospondin receptor); collagen type I receptor (CD36); thrombospondin receptor (CD36); glycoprotein IIIb; glycoprotein IV (platelet); platelet glycoprotein IV deficiency; [THBS — Gene: [08^/ASNSL1] asparagine synthetase-like 1;


  • Gene: [07q112/CD36] antigen CD36 (collagen type I receptor, thrombospondin receptor); collagen type I receptor (CD36); thrombospondin receptor (CD36); glycoprotein IIIb; glycoprotein IV (platelet); platelet glycoprotein IV deficiency; [THBS
  • Gene: [07q112/CYPOR] cytochrome P450 oxidoreductase (NADPH-dependent);
  • Gene: [07q112/SKP1A] S-phase kinase-associated protein 1A (p19A); CDK2/cyclin A-associated protein p19A; RNA polymerase II elongation factor-like protein;
  • Gene: [07q112/ZNF117] zinc finger protein 117 (HPF9);
  • Gene: [07q112/ZNF138] zinc finger protein 138 (clone pHZ-32);
  • Gene: [07q1121/GABPB] GA-binding protein transcription factor, beta subunit (53/47kD); adenovirus E4 gene transcription factor, 53-kD subunit; [GABPB1 ]
  • Gene: [07q1123/ELN] elastin (tropoelastin); supravalvular aortic stenosis (SVAS); Williams-Beuren syndrome (WS; WBS; MIM:194050); hypercalcemia, infantile (with elfin facies); [SVAS WS WBS ]
  • Gene: [07q1123/FZD9] frizzled (Drosophila) homolog 9; [FZD3 ]
  • Gene: [07q1123/GTF2IP1] general transcription factor II, i, pseudogene 1; Williams-Beuren syndrome chromosome region 7; [WBSCR7 ]
  • Gene: [07q1123/GTF2I] general transcription factor II, i; Williams-Beuren syndrome chromosome region 6; Bruton tyrosine kinase associated protein (BAP; 135kD); [WBSCR6 SPIN ]
  • Gene: [07q1123/HIP1] huntingtin interacting protein 1;
  • Gene: [07q1123/LIMK1] LIM domain kinase 1; LIM motif-containing protein kinase 1; Williams-Beuren syndrome (WS; WBS; MIM:194050);
  • Gene: [07q1123/NCF1] neutrophil cytosolic factor 1 (47kD); NADPH oxidase, neutrophil, cytosolic factor 1 (47 kD); chronic granulomatous disease, autosomal 1; [SOC2 CGD1 ]
  • Gene: [07q1123/PTPN12] protein tyrosine phosphatase, non-receptor type 12; protein tyrosine phosphatase G1; colon cancer?;
  • Gene: [07q1123/RFC2] replication factor C (activator 1) 2 (40kD); Williams-Beuren syndrome (WBS; MIM:194050); [WS WBS ]
  • Gene: [07q2/COL1A2] collagen, type I, alpha 2; osteogenesis imperfecta, type III (MIM:259420); osteogenesis imperfecta, type IV (mild; MIM:166220); Ehlers-Danlos syndrome, type VII (MIM:130060); [OI4 ]
  • Gene: [07q2/CYP3A3] cytochrome P450, subfamily IIIA (niphedipine oxidase), polypeptide 3;
  • Gene: [07q2/CYP3A4] cytochrome P450, subfamily IIIA (niphedipine oxidase), polypeptide 4;
  • Gene: [07q2/CYP3A5] cytochrome P450, subfamily IIIA (niphedipine oxidase), polypeptide 5;
  • Gene: [07q2/CYP3A7] cytochrome P450, subfamily IIIA, polypeptide 7;
  • Gene: [07q2/GNAI1] guanine nucleotide binding protein (G protein), alpha inhibiting activity polypeptide 1; adenylate cyclase inhibitor GI, alpha-I1;
  • Gene: [07q2/GNB2] guanine nucleotide binding protein (G protein), beta polypeptide 2; adenylate cyclase modulator G(I,S,T), beta-2;
  • Gene: [07q2/MCM7] minichromosome maintenance deficient (S.cerevisiae) 7; DNA replication licensing factor CDC47; cell division cycle 47 (homolog of CDC47 of S.cerevisiae); [CDC47 ]
  • Gene: [07q2/MTERF] transcription termination factor, mitochondrial;
  • Gene: [07q2/NPTX2] pentraxin II (neuronal);
  • Gene: [07q2/PCOLCE] procollagen C-endopeptidase enhancer;
  • Gene: [07q2/PEX1] peroxisome biogenesis factor 1; peroxin-1; Refsum disease, infantile form (neonatal adrenoleukodystrophy); Zellweger syndrome; [IRD NALD ZS ]
  • Gene: [07q2/PON1] paraoxonase, plasma (paroxonase; arylesterase; esterase A) 1; coronary artery disease, association with the risk of;
  • Gene: [07q2/PON2] paraoxonase, plasma (paroxonase; arylesterase; esterase A) 2; elevated fasting plasma glucose in NIDDM; coronary artery disease, association with;
  • Gene: [07q2/PON3] paraoxonase, plasma (paroxonase; arylesterase; esterase A) 3;
  • Gene: [07q2/SHFM1] split hand/foot malformation (ectrodactyly) type 1; [SHFD1 ECD ]
  • Gene: [07q2/TAC1] tachykinin 1 (substance P, neurokinin 1); tachykinin 2 (substance K, neurokinin A, neurokinin 2, neuromedin L, neurokinin alpha, neuropeptide K, neuropeptide gamma); [NKNA TAC2 ]
  • Gene: [07q2/ZNF139] zinc finger protein 139 (clone pHZ-37);
  • Gene: [07q2/ZNF36] zinc finger protein 36 (KOX 18); [KOX18 ]
  • Gene: [07q2/ZNF38] zinc finger protein 38 (KOX 25); [KOX25 ]
  • Gene: [07q21/CYP51] cytochrome P450, 51 (lanosterol 14-alpha-demethylase);
  • Gene: [07q21/EPO] erythropoietin;
  • Gene: [07q21/FZD1] frizzled (Drosophila) homolog 1;
  • Gene: [07q21/GRM3] glutamate receptor, metabotropic 3;
  • Gene: [07q211/HGF] hepatocyte growth factor (hepapoietin A; scatter factor); lung fibroblast-derived mitogen (hepapoietin A; scatter factor); [SF ]
  • Gene: [07q211/PGY1P] P glycoprotein-1 pseudogene; [MDR2 ]
  • Gene: [07q211/PGY1] P glycoprotein-1/multiple drug resistance 1; multiple drug resistance 1 (P glycoprotein-1); colchicin sensitivity (MIM:120080); [MDR1 CLCS ]
  • Gene: [07q211/PGY3] P glycoprotein-3/multiple drug resistance 3; multiple drug resistance 3 (P glycoprotein-3); [MDR3 ]
  • Gene: [07q211/SRI] sorcin (multiple drug resistance 4); multidrug-resistance complex, class 4; [MDR4 SCN ]
  • Gene: [07q212/FRA7E] fragile site 7q21.2, aphidicolin type, common;
  • Gene: [07q213/CALCR] calcitonin receptor;
  • Gene: [07q213/GNGT1] guanine nucleotide binding protein (G protein), gamma transducing activity polypeptide 1; adenylate cyclase transductor GT, gamma-T1;
  • Gene: [07q213/PDK4] pyruvate dehydrogenase kinase, isoenzyme 4;
  • Gene: [07q22/ACHE] YT blood group (Cartwright; MIM:112100); acetylcholinesterase;
  • Gene: [07q22/CUTL1] cut (Drosophila)-like 1 (CCAAT displacement protein);
  • Gene: [07q22/DLX5] distal-less homeo box 5;
  • Gene: [07q22/DLX6] distal-less homeo box 6;
  • Gene: [07q22/FRA7F] fragile site 7q22, aphidicolin type, common;
  • Gene: [07q22/GUSB] glucuronidase, beta; mucopolysaccharidosis VII (Sly syndrome);
  • Gene: [07q22/LAMB1] laminin, beta 1 (laminin B1);
  • Gene: [07q22/MUC3] mucin 3, intestinal;
  • Gene: [07q22/PLGAI1] plasminogen activator inhibitor, type I (endothelial); [PLANH1 PAI1 ]
  • Gene: [07q22/PMS2L8] postmeiotic segregation increased 2-like 8; [PMSR2 ]
  • Gene: [07q22/PRKAR2B] protein kinase, cAMP-dependent, regulatory subunit, type II, beta;
  • Gene: [07q22/PSMC2] proteasome (prosome, macropain) 26S subunit, ATPase, 2 (homolog of yeast YTA3, CIM5); 26S protease regulatory subunit 7 (mammalian suppressor of sgv-1 of yeast; MSS1); [MSS1 S7 ]
  • Gene: [07q22/RELN] reelin;
  • Gene: [07q22/TFPI2] tissue factor pathway inhibitor 2; placental protein 5;
  • Gene: [07q22/TRIP6] thyroid hormone receptor interactor 6 (OPA-interacting protein 1); [OIP1 ]
  • Gene: [07q22/VGF] VGF nerve growth factor inducible;
  • Gene: [07q22/ZAN] zonadhesin;
  • Gene: [07q22/ZNF188] zinc finger protein 188;
  • Gene: [07q221/AZGP1] alpha-2-glycoprotein 1, zinc pseudogene 1; [AZGP1P1 ]
  • Gene: [07q221/AZG] alpha-2-glycoprotein, zinc; [AZGP1 ]
  • Gene: [07q221/ORC5L] origin recognition complex, subunit 5 (yeast homolog)-like;
  • Gene: [07q3/AOC1] amine oxidase, copper-containing 1; amiloride-sensitive diamine oxidase; amiloride binding protein 1;
  • Gene: [07q3/AUTS1] autism susceptibility 1;
  • Gene: [07q3/BPGM] 2,3-bisphosphoglycerate mutase; hemolytic anemia due to bisphosphoglyceromutase deficiency;
  • Gene: [07q3/CALD1] caldesmon 1; [CDM H-CAD ]
  • Gene: [07q3/CBBA] blue cone pigment (tritanopia); color blindness tritanopic (blue cone pigment); [BCP CBT ]
  • Gene: [07q3/CHRM2] cholinergic receptor, muscarinic 2;
  • Gene: [07q3/CLM] cutis laxa with marfanoid phenotype;
  • Gene: [07q3/CMH6] cardiomyopathy, hypertrophic 6 (with Wolff-Parkinson-White syndrome);
  • Gene: [07q3/D7S437] satellite DNA, minisatellite class (probe 33.15); hypervariable marker for chr 07q3 (minisatellite probe 33.15); [MS3315 ]
  • Gene: [07q3/DFNB13] deafness, autosomal recessive 13;
  • Gene: [07q3/DLD] lipoamide dehydrogenase; lactoacidosis due to lipoamide dehydrogenase deficiency;
  • Gene: [07q3/EPHA1] ephrin receptor EphA1; eph tyrosine kinase 1 (erythropoietin-producing hepatoma amplified sequence);
  • Gene: [07q3/EPHB6] ephrin receptor EphB6; [HEP ]
  • Gene: [07q3/FLN2] filamin 2 (actin-binding protein-280); [ABP-280 ]
  • Gene: [07q3/GNG11] guanine nucleotide binding protein (G protein), gamma polypeptide 11;
  • Gene: [07q3/GRM8] glutamate receptor, metabotropic 8;
  • Gene: [07q3/IMPDH1] IMP (inosine monophosphate) dehydrogenase 1;
  • Gene: [07q3/LQT2] long (electrocardiographic) QT syndrome 2; [HERG ]
  • Gene: [07q3/NEFLL2] neurofilament, light polypeptide-like 2;
  • Gene: [07q3/ODCP] ornithine decarboxylase pseudogene; [ODC2 ]
  • Gene: [07q3/PIP] prolactin-induced protein; [SABP ]
  • Gene: [07q3/PODXL] podocalyxin-like; [PCLP ]
  • Gene: [07q3/PTN] pleiotrophin (heparin binding growth factor 8); neurite growth-promoting factor 1; [NEGF1 ]
  • Gene: [07q3/RP10] retinitis pigmentosa 10 (autosomal dominant);
  • Gene: [07q3/SLC4A2] solute carrier family 4, anion exchanger, member 2; erythrocyte membrane protein band 3-like 1 (non-erythroid); [MPB3L EPB3L1 ]
  • Gene: [07q3/TIM] transforming immortalized mammary (oncogene TIM); guanine nucleotide regulatory protein (tim1); [tim1 ]
  • Gene: [07q31/CAPZA2] capping protein (actin filament) muscle Z-line, alpha 2;
  • Gene: [07q31/DFNB17] deafness, autosomal recessive 17;
  • Gene: [07q31/DRA] protein DRA (down-regulated in adenoma); congenital chloride diarrhea (MIM:214700); [CLD ]
  • Gene: [07q31/GPR37] G protein-coupled receptor 37; endothelin receptor type B-like; [EDNRBL ]
  • Gene: [07q31/MET] MET proto-oncogene tyrosine kinase; hepatocyte growth factor receptor; papillary renal carcinoma;
  • Gene: [07q31/NRCAM] neuronal cell adhesion molecule; [Bravo ]
  • Gene: [07q31/PDS] pendrin (86kD); Pendred syndrome (goitre and sensorineural hearing loss); thyroid hormonogenesis, genetic defect in, IIB; deafness, autosomal recessive 4 (MIM:600791); [DFNB4 ]
  • Gene: [07q31/SPAM1] sperm adhesion molecule 1; sperm surface protein PH-20 (zona pellucida binding); hyaluronidase (hyaluronoglucosaminidase);
  • Gene: [07q31/SPCH1] speech-language disorder 1;
  • Gene: [07q31/WNT2] wingless-type MMTV integration site 2, human homolog; INT-1-like protein 1; [INT1L1 IRP ]
  • Gene: [07q311/ST7] suppression of tumorigenicity 7 (breast?; ovarian?); ovarian carcinoma?; [TSG7 ]
  • Gene: [07q312/CFTR] cystic fibrosis transmembrane conductance regulator; cystic fibrosis (mucoviscidosis; MIM:219700); congenital bilateral aplasia of the vas deferens (MIM:277180); [CF CBAVD ]
  • Gene: [07q312/FRA7G] fragile site 7q31.2, aphidicolin type, common;
  • Gene: [07q313/LEP] leptin (murine obesity homolog); obesity (murine homolog, leptin); [OBS ]
  • Gene: [07q313/PTPRZ1] protein tyrosine phosphatase, receptor type, zeta polypeptide 1;
  • Gene: [07q32/CPA1] carboxypeptidase A1 (pancreatic);
  • Gene: [07q32/IRF5] interferon regulatory factor 5;
  • Gene: [07q32/MEST] mesoderm specific transcript (mouse) homolog; paternally expressed gene 1 (PEG1); [PEG1 ]
  • Gene: [07q32/NDUFA5] NADH dehydrogenase (ubiquinone) 1 alpha subcomplex, 5 (13kD, B13); NADH:ubiquinone oxidoreductase subunit B13;
  • Gene: [07q32/NRF1] nuclear respiratory factor 1;
  • Gene: [07q32/PAX4] paired box homeotic gene 4;
  • Gene: [07q32/ZYX] zyxin;
  • Gene: [07q321/SLOS] Smith-Lemli-Opitz syndrome, type 2?;
  • Gene: [07q323/FRA7H] fragile site 7q32.3, aphidicolin type, common;
  • Gene: [07q33/KEL] Kell blood group (Kell-Cellano system); Kell blood group glycoprotein;
  • Gene: [07q34/BRAFP] murine sarcoma viral (v-raf) oncogene homolog B1 pseudogene;
  • Gene: [07q34/BRAF] murine sarcoma viral (v-raf) oncogene homolog B1;
  • Gene: [07q34/ERH] enhancer of rudimentary (Drosophila) homolog; [DROER ]
  • Gene: [07q34/SSBP] single-stranded DNA-binding protein, mitochondrial;
  • Gene: [07q34/TBXAS1] thromboxane A synthase 1 (platelet, cytochrome P450, subfamily V); thromboxane synthetase deficiency;
  • Gene: [07q35/ALDR1] aldehyde reductase 1 (low Km aldose reductase);
  • Gene: [07q35/CASP2] caspase 2 (NEDD2 apoptosis regulatory gene); protease ICH-1 (isoforms L and S); neural precursor cell expressed, developmentally down-regulated 2; holoprosencephaly?;
  • Gene: [07q35/CLCN1] chloride channel 1, skeletal muscle; Thomsen's disease (myotonia congenita; autosomal dominant; MIM:160800); Becker's disease (generalized myotonia; autosomal recessive; MIM:255700);
  • Gene: [07q35/PRSS1] protease, serine, 1 (trypsin 1); trypsin 1; trypsinogen deficiency; pancreatitis, hereditary (calcific; MIM:167800);
  • Gene: [07q35/PRSS2] protease, serine, 2 (trypsin 2);
  • Gene: [07q35/SMARCD3] SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily d, member 3; chromatin remodeling complex, BRG1-associated factor, 60kD, C; [BAF60C CRACD3 ]
  • Gene: [07q35/TCR1B1C] T cell receptor, Ti-beta-1 subunit, CON-region; [TCRB ]
  • Gene: [07q35/TCR1B1D] T cell receptor, Ti-beta-1 subunit, DIV-segment; [TCRB ]
  • Gene: [07q35/TCR1B1J1] T cell receptor, Ti-beta-1 subunit, J1-segment; [TCRB ]
  • Gene: [07q35/TCR1B1J2] T cell receptor, Ti-beta-1 subunit, J2-segment;
  • Gene: [07q35/TCR1B1J3] T cell receptor, Ti-beta-1 subunit, J3-segment;
  • Gene: [07q35/TCR1B1J4] T cell receptor, Ti-beta-1 subunit, J4-segment;
  • Gene: [07q35/TCR1B1J5] T cell receptor, Ti-beta-1 subunit, J5-segment;
  • Gene: [07q35/TCR1B1J6] T cell receptor, Ti-beta-1 subunit, J6-segment;
  • Gene: [07q35/TCR1B2C] T cell receptor, Ti-beta-2 subunit, CON-region;
  • Gene: [07q35/TCR1B2D] T cell receptor, Ti-beta-2 subunit, DIV-segment;
  • Gene: [07q35/TCR1B2J1] T cell receptor, Ti-beta-2 subunit, J1-segment;
  • Gene: [07q35/TCR1B2J2] T cell receptor, Ti-beta-2 subunit, J2-segment;
  • Gene: [07q35/TCR1B2J3] T cell receptor, Ti-beta-2 subunit, J3-segment;
  • Gene: [07q35/TCR1B2J4] T cell receptor, Ti-beta-2 subunit, J4-segment;
  • Gene: [07q35/TCR1B2J5] T cell receptor, Ti-beta-2 subunit, J5-segment;
  • Gene: [07q35/TCR1B2J6] T cell receptor, Ti-beta-2 subunit, J6-segment;
  • Gene: [07q35/TCR1B2J7] T cell receptor, Ti-beta-2 subunit, J7-segment;
  • Gene: [07q35/TCR1BV10] T cell receptor, Ti-beta subunit, VAR-region 10;
  • Gene: [07q35/TCR1BV11] T cell receptor, Ti-beta subunit, VAR-region 11;
  • Gene: [07q35/TCR1BV12] T cell receptor, Ti-beta subunit, VAR-region 12;
  • Gene: [07q35/TCR1BV13] T cell receptor, Ti-beta subunit, VAR-region 13;
  • Gene: [07q35/TCR1BV14] T cell receptor, Ti-beta subunit, VAR-region 14;
  • Gene: [07q35/TCR1BV15] T cell receptor, Ti-beta subunit, VAR-region 15;
  • Gene: [07q35/TCR1BV16] T cell receptor, Ti-beta subunit, VAR-region 16;
  • Gene: [07q35/TCR1BV17] T cell receptor, Ti-beta subunit, VAR-region 17;
  • Gene: [07q35/TCR1BV18] T cell receptor, Ti-beta subunit, VAR-region 18;
  • Gene: [07q35/TCR1BV19] T cell receptor, Ti-beta subunit, VAR-region 19;
  • Gene: [07q35/TCR1BV1] T cell receptor, Ti-beta subunit, VAR-region 1; [TCRB ]
  • Gene: [07q35/TCR1BV20] T cell receptor, Ti-beta subunit, VAR-region 20;
  • Gene: [07q35/TCR1BV21] T cell receptor, Ti-beta subunit, VAR-region 21;
  • Gene: [07q35/TCR1BV22] T cell receptor, Ti-beta subunit, VAR-region 22;
  • Gene: [07q35/TCR1BV23] T cell receptor, Ti-beta subunit, VAR-region 23;
  • Gene: [07q35/TCR1BV24] T cell receptor, Ti-beta subunit, VAR-region 24;
  • Gene: [07q35/TCR1BV25] T cell receptor, Ti-beta subunit, VAR-region 25;
  • Gene: [07q35/TCR1BV26] T cell receptor, Ti-beta subunit, VAR-region 26;
  • Gene: [07q35/TCR1BV27] T cell receptor, Ti-beta subunit, VAR-region 27;
  • Gene: [07q35/TCR1BV28] T cell receptor, Ti-beta subunit, VAR-region 28;
  • Gene: [07q35/TCR1BV29] T cell receptor, Ti-beta subunit, VAR-region 29;
  • Gene: [07q35/TCR1BV2] T cell receptor, Ti-beta subunit, VAR-region 2;
  • Gene: [07q35/TCR1BV30] T cell receptor, Ti-beta subunit, VAR-region 30;
  • Gene: [07q35/TCR1BV31] T cell receptor, Ti-beta subunit, VAR-region 31;
  • Gene: [07q35/TCR1BV32] T cell receptor, Ti-beta subunit, VAR-region 32;
  • Gene: [07q35/TCR1BV33] T cell receptor, Ti-beta subunit, VAR-region 33;
  • Gene: [07q35/TCR1BV34] T cell receptor, Ti-beta subunit, VAR-region 34;
  • Gene: [07q35/TCR1BV35] T cell receptor, Ti-beta subunit, VAR-region 35;
  • Gene: [07q35/TCR1BV36] T cell receptor, Ti-beta subunit, VAR-region 36;
  • Gene: [07q35/TCR1BV37] T cell receptor, Ti-beta subunit, VAR-region 37;
  • Gene: [07q35/TCR1BV3] T cell receptor, Ti-beta subunit, VAR-region 3;
  • Gene: [07q35/TCR1BV4] T cell receptor, Ti-beta subunit, VAR-region 4;
  • Gene: [07q35/TCR1BV5] T cell receptor, Ti-beta subunit, VAR-region 5;
  • Gene: [07q35/TCR1BV6] T cell receptor, Ti-beta subunit, VAR-region 6;
  • Gene: [07q35/TCR1BV7] T cell receptor, Ti-beta subunit, VAR-region 7;
  • Gene: [07q35/TCR1BV8] T cell receptor, Ti-beta subunit, VAR-region 8;
  • Gene: [07q35/TCR1BV9] T cell receptor, Ti-beta subunit, VAR-region 9;
  • Gene: [07q36/CDK5] cyclin-dependent kinase 5;
  • Gene: [07q36/EN2] homeobox engrailed homolog 2;
  • Gene: [07q36/FRA7I] fragile site 7q36, aphidicolin type, common;
  • Gene: [07q36/GBX1] gastrulation brain homeo box 1;
  • Gene: [07q36/HPFH2] hereditary persistence of fetal hemoglobin, heterocellular 2 (Indian type); F-cell production, heterocellular 2 (Indian type);
  • Gene: [07q36/INSIG1] insulin induced gene 1; [CL-6 ]
  • Gene: [07q36/NOS3] nitric oxide synthase 3 (endothelial cell); hypertension, pregnancy-induced; coronary artery disease, association with;
  • Gene: [07q36/PPD2] preaxial polydactyly, 2; [PPD-2 ]
  • Gene: [07q36/PTPRN2] protein tyrosine phosphatase, receptor type, N polypeptide 2; protein tyrosine phosphatase, receptor type, N-beta; islet cell antigen-related protein tyrosine phosphatase; phogrin;
  • Gene: [07q36/RHEB2] Ras homolog enriched in brain 2; [RHEB ]
  • Gene: [07q36/SAAG] sacral agenesis, hereditary (Currarino triad);
  • Gene: [07q36/SHH] sonic hedgehog (Drosophila) homolog; holoprosencephaly 3 (MIM:142945); [HLP3 HPE3 ]
  • Gene: [07q361/HTR5A] 5-hydroxytryptamine (serotonin) receptor 5A;
  • Gene: [07q361/XRCC2] X-ray repair complementing defective repair in Chinese hamster cells 2;
  • Gene: [07q363/VIPR2] vasoactive intestinal peptide receptor 2;
  • Gene: [07^/CDK6] cyclin-dependent kinase 6 (Cdc2-related kinase);
  • Gene: [07^/COX5BL3] cytochrome c oxidase subunit Vb-like 3;
  • Gene: [07^/DPP6] dipeptidylpeptidase-like protein VI;
  • Gene: [07^/EPHB4] ephrin receptor EphB4; hepatoma transmembrane tyrosine kinase;
  • Gene: [07^/ERV3] endogenous retroviral sequence 3; zinc finger protein H-plk;
  • Gene: [07^/FDPSL2] farnesyldiphosphate synthetase (dimethylallyltransferase)-like 2; farnesyldiphosphate synthetase (geranyl-trans-transferase)-like 2;
  • Gene: [07^/GAPDL13] glyceraldehyde-3-phosphate dehydrogenase-like 13;
  • Gene: [07^/GCF1] growth control factor 1;
  • Gene: [07^/HSPB1] heat shock 27kD protein 1; [HSP27 ]
  • Gene: [07^/INSRL] insulin receptor-like;
  • Gene: [07^/NHPC2] non-histone protein 2, chromosomal; [NHCP1 NHCP2 ]
  • Gene: [07^/PHKG1] phosphorylase kinase, gamma 1 (muscle);
  • Gene: [07^/POLD2] polymerase (DNA directed), delta 2, regulatory subunit (50kD);
  • Gene: [07^/PRPS3] phosphoribosyl pyrophosphate synthetase 3;
  • Gene: [07^/PYHG3] protein spot in 2-D gels (MM 106 kD);
  • Gene: [07^/PYHG8] protein spot in 2-D gels (MM 80 kD);
  • Gene: [07^/RNY1] RNA, Y1 small cytoplasmic (associated with Ro protein);
  • Gene: [07^/RNY3] RNA, Y3 small cytoplasmic (associated with Ro protein);
  • Gene: [07^/RNY4] RNA, Y4 small cytoplasmic (associated with Ro protein);
  • Gene: [07^/S7] surface antigen S7 (chromosome 7; SA7-2; Cicurel-Croce); [S6 SA7-2 ]
  • Gene: [07^/SUP45L3] sup45 (yeast omnipotent suppressor 45) homolog-like 3;
  • Gene: [07^/UBE2H] ubiquitin-conjugating enzyme E2H (homologous to yeast UBC8; 21kD);
  • Gene: [07^/UP] uridine phosphorylase;
  • Gene: [07^/ZNT3] zinc transporter 3;
  • Gene: [07^/ZP3A] zona pellucida glycoprotein 3A (sperm receptor);
  • Gene: [07^/ZP3B] zona pellucida glycoprotein 3B (sperm receptor);
  • Gene: [08p/CYRN1] cyritestin 1; [ADAM3 ]
  • Gene: [08p/EPHX2] epoxide hydrolase 2, cytoplasmic;
  • Gene: [08p/FAK2] focal adhesion kinase 2;
  • Gene: [08p/GNRH1] gonadotropin-releasing hormone 1 (GNRH1; gonadoliberin); luteinizing hormone, releasing hormone (LHRH; gonadoliberin); prolactin release-inhibiting factor; adrenal hypoplasia with absent luteinizing hormone? (MIM:202150);
  • Gene: [08p/HGL] heregulin, alpha (45kD, ERBB2 p185-activator);
  • Gene: [08p/PTNKAP1] Pre-T/NK cell associated protein (1D12A2);
  • Gene: [08p/STC] stanniocalcin;
  • Gene: [08p1/ADRB3] adrenergic, beta-3-, receptor;
  • Gene: [08p1/DUSP4] dual specificity phosphatase 4 (EC:3.1.3.48 and EC:3.1.3.16); MAP kinase phosphatase 2; threonine-tyrosine phosphatase 1;
  • Gene: [08p1/GPR9] G protein-coupled receptor 9;
  • Gene: [08p1/IKBKB] inhibitor of kappa light polypeptide gene enhancer in B-cells, kinase beta;
  • Gene: [08p1/INDO] indoleamine-pyrrole 2,3 dioxygenase;
  • Gene: [08p1/PLGAT] plasminogen activator, tissue;
  • Gene: [08p1/POLB] polymerase (DNA directed), beta;
  • Gene: [08p1/PPP2CB] protein phosphatase 2 (formerly 2A), catalytic subunit, beta isoform;
  • Gene: [08p1/REP8] reproduction/chromosome 8; [D8S2298E ]
  • Gene: [08p11/CLAPM2] clathrin-associated/assembly/adaptor protein, medium 2; clathrin adaptor protein 47; [AP47 ]
  • Gene: [08p11/MOZ] monocytic leukaemia zinc finger protein (acetyltransferase?); monocytic leukaemia?;
  • Gene: [08p112/ANK1] ankyrin 1, erythrocytic (ankyrin R); spherocytosis, type II; [SPH2 ]
  • Gene: [08p112/CHRNB3] cholinergic receptor, nicotinic, beta polypeptide 3 (neuronal);
  • Gene: [08p112/FTNB] fertilin beta; [ADAM2 ]
  • Gene: [08p112/STAR] steroidogenic acute regulatory protein; lipoid congenital adrenal hyperplasia;
  • Gene: [08p12/EIF4EBP1] eukaryotic translation initiation factor 4E binding protein 1; [PHAS-I ]
  • Gene: [08p12/FGFR1] fibroblast growth factor receptor 1; fms-related tyrosine kinase 2; Pfeiffer type acrocephalosyndactyly (MIM:101600);
  • Gene: [08p12/GTF2E2] general transcription factor IIE, polypeptide 2 (beta subunit, 34kD);
  • Gene: [08p12/HR] hairless (mouse) homolog (transcription factor?); alopecia universalis congenitalis, autosomal recessive (MIM:203655);
  • Gene: [08p12/WRN] Werner syndrome;
  • Gene: [08p2/AAC1] arylamine acetyltransferase 1 (N-acetyltransferase 1); arylamide acetylase 1;
  • Gene: [08p2/ATP6B2] ATPase, H+ transporting, lysosomal (vacuolar proton pump), beta polypeptide, 56/58kD, isoform 2 (brain); vacuolar proton pump 3 (58kD subunit), isoform 2 (brain);
  • Gene: [08p2/BLK] protein tyrosine kinase, B-lymphocyte specific;
  • Gene: [08p2/DCR1] decoy receptor 1; cytotoxic ligand TRAIL receptor 3; [DR6 TRAIL-R3 ]
  • Gene: [08p2/DEFA5] defensin, alpha 5, Paneth cell-specific; [DEF5 ]
  • Gene: [08p2/DEFA6] defensin, alpha 6, Paneth cell-specific; [DEF6 ]
  • Gene: [08p2/DEFB2] defensin, beta 2; skin-antimicrobial-peptide 1; [HBD-2 SAP1 ]
  • Gene: [08p2/DPYSL2] dihydropyrimidinase-like 2; collapsin response mediator protein 2; [DHPRP2 CRMP2 ]
  • Gene: [08p2/DR5] death receptor 5; cytotoxic ligand TRAIL receptor 2; [TRAIL-R2 ]
  • Gene: [08p2/EGR3] early growth response 3 (transcription factor); zinc-finger protein EGR3;
  • Gene: [08p2/FDFT1] farnesyl-diphosphate farnesyltransferase 1;
  • Gene: [08p2/GATA4] GATA-binding protein 4 (transcription factor);
  • Gene: [08p2/KWE] keratolytic winter erythema (Oudtshoorn skin disease);
  • Gene: [08p2/PCM1] pericentriolar material 1;
  • Gene: [08p2/PHP32] putative heart protein (32kD);
  • Gene: [08p2/PRLTS] PDGF-receptor beta-like tumor suppressor; platelet-derived growth factor receptor-like; [PDGFRBL ]
  • Gene: [08p2/SLC7A2] solute carrier family 7 (cationic amino acid transporter, y+ system), member 2; amino acid transporter, cationic 2 (low-affinity); [ATRC2 HCAT2 ]
  • Gene: [08p21/ADRA1C] adrenergic, alpha-1C-, receptor; [ADRA1L1 ]
  • Gene: [08p21/BMP1] bone morphogenetic protein 1 (zinc metalloprotease?); procollagen C-proteinase; tolloid (Drosophila)-like;
  • Gene: [08p21/BN51TL1] BN51 (BHK21) temperature sensitivity complementing-like 1;
  • Gene: [08p21/CHRNA2] cholinergic receptor, nicotinic, alpha polypeptide 2 (neuronal); [NACHRA2 ]
  • Gene: [08p21/CLU] clusterin (complement lysis inhibitor, SP-40,40, apolipoprotein J); sulfated glycoprotein 2 (testosterone-repressed prostate message 2); [CLI SGP-2]
  • Gene: [08p21/DCR2] decoy receptor 2; cytotoxic ligand TRAIL receptor 4 (truncated death domain; TRUNDD); [TRAIL-R4 ]
  • Gene: [08p21/EXTL3] exostoses (multiple)-like 3; exostoses (multiple)-related 1; [EXTR1 ]
  • Gene: [08p21/GFRA2] GDNF family receptor alpha 2; glial cell line derived neurotrophic factor receptor, beta; neurturin receptor alpha; TGF-beta related neurotrophic factor 2; [GDNFRB NTNRA ]
  • Gene: [08p21/NEFL] neurofilament, light polypeptide (68kD); [NF68 ]
  • Gene: [08p21/NKX3A] NK homeobox (Drosophila), family 3, A; [NKX3.1 ]
  • Gene: [08p21/PNOC] propronociceptin (orphanin FQ); [FQ ]
  • Gene: [08p21/SFTPC] surfactant, pulmonary-associated protein 3A (SP-C; 5kD); [SFTP2 PSPC ]
  • Gene: [08p211/EPB49] erythrocyte membrane protein band 4.9 (dematin);
  • Gene: [08p211/GSR] glutathione reductase; hemolytic anemia due to deficiency of glutathione reductase;
  • Gene: [08p211/GULOP] L-gulonolactone oxidase pseudogene; [GGLOP ]
  • Gene: [08p213/SLC18A1] solute carrier family 18 (vesicular monoamine), member 1; [VAT1 CGAT ]
  • Gene: [08p22/AAC2] arylamide acetylase 2; arylamine acetyltransferase 2 (N-acetyltransferase 2); isoniazid inactivation (acetylator phenotype);
  • Gene: [08p22/CTSB] cathepsin B; amyloid precursor protein secretase;
  • Gene: [08p22/LPL] lipoprotein lipase; hyperlipoproteinemia, type I (chylomicronemia syndrome);
  • Gene: [08p22/MSR1] macrophage scavenger receptor 1;
  • Gene: [08p23/ADE2C1] phosphoribosylaminoimidazole carboxylase 2 (AIR carboxylase; EC:4.1.1.21); phosphoribosylaminoimidazole succinocarboxamide synthetase 2 (SAICAR synthetase; EC:6.3.2.6); ade2 (S.cerevisiae) complementing; multifunctional
  • Gene: [08p23/CLN8] ceroid-lipofuscinosis, neuronal 8; epilepsy, progressive with mental retardation; [EPMR ]
  • Gene: [08p23/DEFA1] defensin, alpha 1 and 3 (myeloid-related sequence, neutrophil specific); [MRS HNP1 ]
  • Gene: [08p23/DEFA4] defensin, alpha 4, corticostatin; [DEF4 ]
  • Gene: [08p23/DEFB1] defensin, beta 1; [HBD-1 ]
  • Gene: [08p23/F7R] coagulation factor VII regulator; proconvertin regulator; [F7E ]
  • Gene: [08q/CCAL2] chondrocalcinosis 2; calcium pyrophosphate-deposition disease, early onset osteoarthritis; [CCAL1 CPDD ]
  • Gene: [08q/CMT4A] Charcot-Marie-Tooth neuropathy 4A;
  • Gene: [08q/FEB1] febrile convulsions, familial, 1 (MIM:121210);
  • Gene: [08q/GEM] GTP-binding mitogen-induced T-cell protein overexpressed in skeletal muscle;
  • Gene: [08q/GPB] beta-glycerolphosphatase;
  • Gene: [08q/PDE7A] phosphodiesterase 7A, high-affinity cAMP-specific;
  • Gene: [08q/RPL7] ribosomal protein L7;
  • Gene: [08q1/CYP7A1] cytochrome P450, subfamily VIIA (cholesterol 7 alpha-monooxygenase), polypeptide 1;
  • Gene: [08q1/IL7] interleukin 7 (pre-lymphoid cells proliferation factor);
  • Gene: [08q11/CEBPD] CCAAT/enhancer binding protein (C/EBP), delta;
  • Gene: [08q11/MOS] Moloney murine sarcoma viral oncogene homolog;
  • Gene: [08q11/SLUG1] neural crest transcription factor SLUG (zinc finger protein);
  • Gene: [08q112/MCM4] minichromosome maintenance deficient (S.cerevisiae) 4; cell division cycle 21 (homolog of S.pombe CDC21 and S.cerevisiae CDC54); DNA replication licensing factor MCM4; [CDC21 CDC54 ]
  • Gene: [08q112/OPRK1] opioid receptor, kappa 1;
  • Gene: [08q112/PRKDC] protein kinase, DNA-activated, catalytic polypeptide (p350); hyper-radiosensitivity of murine scid mutation, complementing 1 (HYRC1); X-ray repair complementing defective repair in Chinese hamster cells 7 (XRCC7); agamm
  • Gene: [08q12/PLAG1] pleiomorphic adenoma gene 1; zinc finger protein PLAG1;
  • Gene: [08q13/CRH] corticotropin releasing hormone; [CRF ]
  • Gene: [08q13/FRA8F] fragile site 8q13, unclassified type, rare;
  • Gene: [08q13/LYN] tyrosine kinase-like oncogene LYN; Yamaguchi sarcoma viral related oncogene homolog;
  • Gene: [08q13/TERF1] telomeric repeat binding factor 1; [TRF1 ]
  • Gene: [08q13/TTPA] tocopherol (alpha) transfer protein; ataxia (Friedreich-like) with selective vitamin E deficiency (MIM:277460); [AVED ]
  • Gene: [08q133/EYA1] eyes absent (Drosophila) homolog 1; branchio-oto-renal dysplasia (Melnick-Fraser syndrome; MIM:113650); [BOR ]
  • Gene: [08q133/NDUFB9] NADH dehydrogenase (ubiquinone) 1 beta subcomplex, 9 (22kD, B22); NADH:ubiquinone oxidoreductase, subunit B22 (UQOR22);
  • Gene: [08q2/BN51T] BN51 (BHK21) temperature sensitivity complementing; [TSBN51 ]
  • Gene: [08q2/CALB1] calbindin 1 (27 kD); [CALB CAB27 ]
  • Gene: [08q2/COH1] Cohen syndrome 1; [CHS1 ]
  • Gene: [08q2/CPP] ceruloplasmin (ferroxidase) preudogene;
  • Gene: [08q2/EIF3S6] eukaryotic translation initiation factor 3, subunit 6 (48kD); murine mammary tumor integration site 6 (oncogene homolog); [INT6 ]
  • Gene: [08q2/ENKA] enkephalin A (preproenkephalin A); [PENK ]
  • Gene: [08q2/FZD6] frizzled (Drosophila) homolog 6; [Hfz6 ]
  • Gene: [08q2/GLYB] glycine B complementing;
  • Gene: [08q2/PMP2] peripheral myelin protein 2; fatty acid binding protein 8; [FAB8 ]
  • Gene: [08q2/SDC2] syndecan 2; heparan sulfate proteoglycan 1 (cell surface-associated, fibroglycan, 48/90 kDa); [HSPG HSPG1 ]
  • Gene: [08q2/SGM1] segmentation syndrome 1 (Klippel-Feil syndrome); [KFM KFS ]
  • Gene: [08q2/SLA] Src-like-adapter;
  • Gene: [08q2/SNT2B1] syntrophin, beta 1 (dystrophin-associated protein A1, 59kD, basic component 1);
  • Gene: [08q21/CYP11B1] cytochrome P450, subfamily XIB (steroid 11-beta-hydroxylase), polypeptide 1; steroid 11-beta-hydroxylase (adrenal hyperplasia IV); corticosterone methyl oxidase 1 (CMO I); adrenal hyperplasia IV (steroid 11-beta-hydrox
  • Gene: [08q21/CYP11B2] cytochrome P450, subfamily XIB (steroid 11-beta-hydroxylase), polypeptide 2; steroid 11-beta-hydroxylase B2 (aldosterone synthase; ALDOS); aldosterone deficiency II; hypoaldosteronism II (corticosterone methyl oxidase
  • Gene: [08q21/IMPA1] inositol(myo)-1(or 4)-monophosphatase 1;
  • Gene: [08q21/TPD52] tumor protein D52; [D52 ]
  • Gene: [08q211/PXMP3] peroxisomal membrane protein 3 (35kD, Zellweger syndrome); peroxin-2; peroxisome biogenesis disorder (MIM:601539), complementation group 10; Zellweger syndrome 3; [PEX2 ZWS3 ]
  • Gene: [08q211/SOX5P] SRY (sex determining region Y)-box 5 pseudogene;
  • Gene: [08q213/NBS1] nibrin (p95 protein of Mre11/Rad50 complex); Nijmegen breakage syndrome 1 (Seemanova syndrome II; MIM:251260); [NBS1 p95 ATV ]
  • Gene: [08q22/CA1] carbonic anhydrase I (erythrocytic A);
  • Gene: [08q22/CA2] carbonic anhydrase II (erythrocytic B); osteopetrosis with renal tubular acidosis (CA-II deficiency); Guibaud-Vainsel-Sly syndrome (osteopetrosis; CA-II deficiency);
  • Gene: [08q22/CA3] carbonic anhydrase III, muscle specific;
  • Gene: [08q22/CBFA2T1] core-binding factor, runt domain, alpha subunit 2; translocated to, 1 (cyclin D-related); acute myelogenous leukemia 1 translocation 1, cyclin D-related; [AML1T1 ]
  • Gene: [08q22/KCNS2] potassium voltage-gated channel, delayed-rectifier, subfamily S, member 2; [Kv9.2 ]
  • Gene: [08q22/MOSL] Moloney murine sarcoma viral oncogene homolog-like;
  • Gene: [08q22/MYBL1] avian myeloblastosis viral (v-myb) oncogene homolog-like 1; [AMYB ]
  • Gene: [08q22/ODF1] outer dense fiber of sperm tails 1; [ODF ]
  • Gene: [08q22/PCSP] perchloric acid-soluble protein (p14.5; tumor antigen UK114); [PSP UK114 ]
  • Gene: [08q22/POP1] POP1 (processing of precursor RNAs) homolog;
  • Gene: [08q22/SPAG1] sperm associated antigen 1; sperm protein, infertility-related (75kD); [SP75 ]
  • Gene: [08q22/UQCRB] ubiquinol-cytochrome c reductase binding protein;
  • Gene: [08q221/CDH17] cadherin 17 (LI-cadherin; liver-intestine); human peptide transporter 1; [HPT1 ]
  • Gene: [08q221/FRA8B] fragile site 8q22.1, aphidicolin type, common;
  • Gene: [08q223/FRA8A] fragile site 8q22.3, folic acid type, rare;
  • Gene: [08q23/COL14A1] undulin (fibronectin-tenascin-related); collagen, type XIV, alpha 1; [UND ]
  • Gene: [08q23/GLC1D] glaucoma 1, open angle, D (adult-onset);
  • Gene: [08q23/MJDL1] Machado-Joseph disease-like-1;
  • Gene: [08q23/TRHR] thyrotropin-releasing hormone receptor;
  • Gene: [08q24/ADCY8] adenylate cyclase 8 (brain);
  • Gene: [08q24/ANX13] annexin XIII, intestine specific;
  • Gene: [08q24/BAI1] brain-specific angiogenesis inhibitor 1;
  • Gene: [08q24/BVR1] Burkitt lymphoma variant rearranging region 1; [BL ]
  • Gene: [08q24/EBS1] epidermolysis bullosa simplex 1 (Ogna);
  • Gene: [08q24/EGI] epilepsy, generalized, idiopathic;
  • Gene: [08q24/GPR20] G protein-coupled receptor 20;
  • Gene: [08q24/HPV18I1] human papillomavirus (type 18) integration site 1; [D8S37 ]
  • Gene: [08q24/KCNQ3] potassium voltage-gated channel, KQT-like subfamily, member 3; epilepsy, benign neonatal 2 (MIM:121201); benign familial neonatal convulsions 2 (MIM:121201);
  • Gene: [08q24/LY6] retinoic acid induced gene E; [RIGE ]
  • Gene: [08q24/PLA2L] phospholipase A2-like;
  • Gene: [08q24/PLEC1] plectin 1, intermediate filament binding protein, 500kD; muscular dystrophy with epidermolysis bullosa simplex (MIM:226670); [PCN ]
  • Gene: [08q24/PTK2] protein tyrosine kinase PTK2; focal adhesion kinase 1;
  • Gene: [08q24/RPL8] ribosomal protein L8;
  • Gene: [08q24/TG] thyroglobulin; multinodular goitre 1 (MIM:138800); [MNG1 ]
  • Gene: [08q24/VMD1] vitelliform macular dystrophy, atypical;
  • Gene: [08q24/ZNF16] zinc finger protein 16 (KOX 9); [KOX9 ]
  • Gene: [08q241/FRA8C] fragile site 8q24.1, aphidicolin type, common;
  • Gene: [08q241/FRA8E] fragile site 8q24.1, distamycin A type, rare;
  • Gene: [08q241/MLVI4] Moloney murine leukemia virus (MoMuLV) integration site 4 homolog;
  • Gene: [08q241/MYCA] mouse pvt-1 oncogene homolog, myc-activator; retrovirus HTLV-I insertion site?; adult T cell leukaemia, retrovirus associated (HTLV-I atl); [PVT1 PVTL ATL ]
  • Gene: [08q241/MYC] avian myelocytomatosis viral oncogene homolog;
  • Gene: [08q241/NOV] nephroblastoma overexpressed gene;
  • Gene: [08q241/PDNP2] alkaline phosphodiesterase I (EC:3.1.4.1); nucleotide pyrophosphatase 2 (EC:3.6.1.9); autotaxin;
  • Gene: [08q241/SQLE] squalene epoxidase;
  • Gene: [08q241/ZNF34] zinc finger protein 34 (KOX 32); [KOX32 ]
  • Gene: [08q2411/EXT1] exostosin 1; exostoses (multiple) 1; trichorhinophalangeal syndrome, type II (Langer-Giedion syndrome; MIM:150230); [TRPS2 ]
  • Gene: [08q2411/TRPS1] trichorhinophalangeal syndrome, type I; trichorhinophalangeal syndrome, type II (Langer-Giedion syndrome; MIM:150230); trichorhinophalangeal syndrome, recessive form (MIM:275500); [LGCR TRPS2 ]
  • Gene: [08q2413/RPL30] ribosomal protein L30;
  • Gene: [08q242/PSCA] prostate stem cell antigen; prostate cancer?;
  • Gene: [08q243/CYC1] cytochrome c-1 (mitochondrial);
  • Gene: [08q243/FRA8D] fragile site 8q24.3, aphidicolin type, common;
  • Gene: [08q243/GPT] glutamic-pyruvate transaminase; alanine aminotransferase 1, soluble;
  • Gene: [08q243/HKR4] chromatin-associated HKR-phosphoprotein 4 (oncogene HKR4/GLI4); zinc finger oncoprotein HKR4 (GLI4); GLI-Kruppel family member HKR4; [GLI4 ]
  • Gene: [08q243/HSF1] heat shock transcription factor 1; [HSPF1 HSTF1]
  • Gene: [08q243/ZNF7] zinc finger protein 7 (KOX 4, clone HF.16); [KOX4 ]
  • Gene: [08^/ACTBP6] actin, beta pseudogene 6;
  • Gene: [08^/ASNSL1] asparagine synthetase-like 1;