Gene: [03q13/MOX2] antigen MOX2 (monoclonal antibody MRC-OX2); MRC OX-2 membrane glycoprotein; [MOX1 ] — Gene: [05p13/OXCT] 3-oxoacid CoA transferase (succinyl CoA:); ketoacidosis of infancy (succinyl CoA: 3-oxoacid CoA transferase deficiency);


  • Gene: [03q13/MOX2] antigen MOX2 (monoclonal antibody MRC-OX2); MRC OX-2 membrane glycoprotein; [MOX1 ]
  • Gene: [03q13/UMPS] orotate phosphoribosyl transferase (EC:2.4.2.10; OPRT); orotidine-5'-phosphate decarboxylase (EC:4.1.1.23; UMPS); uridine monophosphate synthetase (EC:4.1.1.23; oroticaciduria I/II); oroticaciduria I (UMPS/OPRT deficiency
  • Gene: [03q131/MHS4] malignant hyperthermia susceptibility 4;
  • Gene: [03q133/DRD3] dopamine receptor D3;
  • Gene: [03q1331/GOLGB1] Golgi autoantigen, golgin subfamily b, macrogolgin (golgin-372, with transmembrane signal), 1; giantin; [GCP GCP372 ]
  • Gene: [03q2/ACPPS] acid phosphatase, prostate-specific;
  • Gene: [03q2/AGTR1A] angiotensin II receptor 1A; [AGTR1 ]
  • Gene: [03q2/APOD] apolipoprotein D;
  • Gene: [03q2/ATR] ataxia telangiectasia and Rad3 (S.pombe) related; FRAP-related protein 1; [FRP1 ]
  • Gene: [03q2/CLCN2] chloride channel 2;
  • Gene: [03q2/CPA3] carboxypeptidase A3 (mast cell);
  • Gene: [03q2/DGKG] diacylglycerol kinase, gamma (90kD);
  • Gene: [03q2/DM2] dystrophia myotonica type 2 (atypical myotonic dystrophy); myotonic dystrophy type 2;
  • Gene: [03q2/ELNL1] elastin-like 1;
  • Gene: [03q2/EPHB1] ephrin receptor EphB1; eph tyrosine kinase 2;
  • Gene: [03q2/EPHB3] ephrin receptor EphB3; eph-like tyrosine kinase 2 (ETK2; human embryo kinase 2);
  • Gene: [03q2/FTHL4] ferritin, heavy polypeptide-like 4;
  • Gene: [03q2/GLC1C] glaucoma 1, open angle, C (middle-onset);
  • Gene: [03q2/GM2AP] GM2 ganglioside activator protein pseudogene;
  • Gene: [03q2/GTF2E1] general transcription factor IIE, polypeptide 1 (alpha subunit, 56kD);
  • Gene: [03q2/GYG] glycogenin;
  • Gene: [03q2/HGD] homogentisate 1,2-dioxygenase (homogentisate oxidase); alkaptonuria;
  • Gene: [03q2/HRY] hairy (Drosophila)-homolog;
  • Gene: [03q2/IL12A] interleukin 12, alpha (cytotoxic lymphocyte maturation factor 1; p35); natural killer cell stimulatory factor 1 (interleukin 12, alpha); [NKSF1 ]
  • Gene: [03q2/LPP] LIM domain-containing preferred translocation partner in lipoma;
  • Gene: [03q2/M3S1] membrane component, chromosome 3, surface marker 1;
  • Gene: [03q2/MFI2] antigen p97 (melanoma associated) identified by monoclonal antibodies 133.2 and 96.5;
  • Gene: [03q2/OPA1] optic atrophy 1 (autosomal dominant, Kjer type); [OAK ]
  • Gene: [03q2/PABPL1] poly(A)-binding protein-like 1; [PAB1 ]
  • Gene: [03q2/PBXP1] homeobox protein PBX pseudogene 1; transcription factor pseudogene 1, pre-B-cell leukemia-associated; [PBX2 ]
  • Gene: [03q2/PCCB] propionyl-CoA carboxylase, beta polypeptide; hyperglycinemia II (propionicacidemia, glycinemia ketotic II);
  • Gene: [03q2/PLD1] phospholipase D1, phosphatidylcholine-specific;
  • Gene: [03q2/PLOD2] procollagen-lysine, 2-oxoglutarate 5-dioxygenase (lysine hydroxylase) 2;
  • Gene: [03q2/PRSS5] protease, serine, 5 (mannose-binding protein-associated); complement C4/C2 activating component of Ra-reactive factor (CRARF);
  • Gene: [03q2/RASA2] RAS p21 protein activator 2; GTPase-activating protein of RAS (GAP1M); [GAP1M ]
  • Gene: [03q2/RBPC1] retinol-binding protein 1, cellular; [CRBP1 RBP1]
  • Gene: [03q2/RBPC2] retinol-binding protein 2, cellular; [CRBP2 RBP2]
  • Gene: [03q2/RHO] rhodopsin (visual pigment apoprotein); retinitis pigmentosa 4, (autosomal dominant; rhodopsin-related); congenital stationary night blindness 4; [RP4 RP5 CSNB4 ]
  • Gene: [03q2/RPN1] ribophorin 1;
  • Gene: [03q2/SEX4] transmembrane protein NOV;
  • Gene: [03q2/SHOT] short stature homeobox homolog;
  • Gene: [03q2/SIAT1] sialyltransferase 1 (beta-galactoside alpha-2,6-sialytransferase); antigen CD75;
  • Gene: [03q2/SI] glucosidase, oligo-1,6- (isomaltase: EC:3.2.1.10); glucosidase, sucrose alpha- (sucrase: EC:3.2.1.48); disaccharide intolerance I (sucrase deficiency I);
  • Gene: [03q2/SMARCA3] SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 3; SNF2 (sucrose nonfermenting, yeast, homolog)-like 3; helicase-like transcription factor; [SNF2L3 HLTF ]
  • Gene: [03q2/SOX2] SRY (sex determining region Y)-box 2;
  • Gene: [03q2/USH3] Usher syndrome 3;
  • Gene: [03q21/BCPM] benign chronic pemphigus (Hailey-Hailey disease);
  • Gene: [03q21/CD80] CD80 antigen (CD28 antigen ligand 1, B7-1 antigen); antigen CD28 ligand 1 (T lymphocyte activation antigen CD80; antigen B7-1); [CD28LG1 ]
  • Gene: [03q21/CD86] CD86 antigen (CD28 antigen ligand 2, B7-2 antigen); antigen CD28 ligand 2 (T lymphocyte activation antigen CD86; antigen B7-2); [CD28LG2 ]
  • Gene: [03q21/CHEL1] butyrylcholinesterase (cholinesterase 1, serum)-like 1; [BCHEL1 ]
  • Gene: [03q21/GATA2] GATA-binding protein 2 (endothelial transcription factor; p45);
  • Gene: [03q21/LAMRL1] laminin receptor-like 1;
  • Gene: [03q21/MCM2] minichromosome maintenance deficient (S.cerevisiae) 2 (mitotin); cell division cycle-like 1 (mitotin); DNA replication licensing factor MCM2 (nuclear protein BM28); [CDC19 CDCL1 ]
  • Gene: [03q21/NCK] melanoma NCK protein; non-catalytic region of tyrosine kinase;
  • Gene: [03q21/RAB7] oncogene RAS-family, member rab7; [RAB7L ]
  • Gene: [03q21/RPL32] ribosomal protein L32;
  • Gene: [03q21/TF] transferrin (iron-binding serum glycoprotein); alcohol abuse-depended liver dysfunction (predisposition?);
  • Gene: [03q21/ZNF148] zinc finger protein 148 (clone pHZ-52); zinc binding protein 89 (89kD); T-cell receptor, beta V8 binding protein, CACCC box-binding protein; [ht-beta ]
  • Gene: [03q211/CSRP2P] cysteine and glycine-rich protein 2 pseudogene;
  • Gene: [03q22/RYK] RYK receptor-like tyrosine kinase;
  • Gene: [03q23/BPES] blepharophimosis, epicanthus inversus and ptosis;
  • Gene: [03q23/TFDP2] transcription factor Dp-2 (E2F dimerization partner 2); [DP2 ]
  • Gene: [03q24/GMPS] guanine monophosphate synthetase;
  • Gene: [03q24/ZIC1] Zic family member 1 (odd-paired Drosophila homolog); zinc finger protein 201; [ZNF201 ]
  • Gene: [03q25/CP] ceruloplasmin (ferroxidase); hypoceruloplasminemia (aceruloplasminemia);
  • Gene: [03q25/FRA3D] fragile site 3q25, aphidicolin type, common;
  • Gene: [03q25/IGKJRB1] immunoglobulin kappa J region recombination signal binding protein 1;
  • Gene: [03q25/MME] metalloendopeptidase, membrane neutral (CD10; enkephalinase); lymhoblastic acute leukemia antigen CALLA (CD10; enkephalinase);
  • Gene: [03q25/PTX3] pentraxin 3 (rapidly induced by IL-1 beta; pentaxin 3); [TSG14 ]
  • Gene: [03q25/SIAH2] seven in absentia (Drosophila) homolog 2;
  • Gene: [03q251/MLF1] myeloid leukemia factor 1; myelodysplastic syndrome and acute myeloid leukemia with t(3;5)(q25.1;q35);
  • Gene: [03q252/CHE1] butyrylcholinesterase (cholinesterase 1, serum); acylcholin acylhydrolase (serum cholinesterase 1); pseudocholinesterase deficiency (suxamethonium sensitivity);
  • Gene: [03q26/ECT2] epithelial cell transforming sequence 2 oncogene;
  • Gene: [03q26/EVI1] ecotropic viral integration site 1;
  • Gene: [03q26/MDS1] myelodysplasia syndrome 1;
  • Gene: [03q26/OTM] oligodendrocyte transmembrane protein; [OSP ]
  • Gene: [03q26/PI12] protease inhibitor 12 (neuroserpin);
  • Gene: [03q26/RPL22] ribosomal protein L22; Epstein-Barr associated protein; [EAP ]
  • Gene: [03q26/SLC2A2] solute carrier family 2 (facilitated glucose transporter), member 2; glucose transporter 2 (liver); Fanconi-Bickel syndrome (hepatorenal glycogenosis with renal Fanconi syndrome; MIM:227810); hepatic glycogenosis with a
  • Gene: [03q26/TRAIL] 酝-related apoptosis-inducing ligand; Apo-2 ligand; tumor necrosis factor ligand superfamily, member 10; [Apo-2L ]
  • Gene: [03q261/KCNA1B] potassium voltage-gated channel, shaker-related subfamily, member 1 beta-1 subunit; [Kvb1.1 Kvb1.3 ]
  • Gene: [03q263/CDL1] Cornelia de Lange syndrome 1; [CDL ]
  • Gene: [03q263/PIK3CA] phosphatidylinositol 3-kinase, catalytic, alpha polypeptide;
  • Gene: [03q27/AHSG] alpha-2-HS-glycoprotein (A/B-polypeptides); [HSGA A2HS ]
  • Gene: [03q27/BCL6] zinc finger protein 51; B-cell chronic lymphatic leukemia 6 (B-CLL: lymphoma 6); [ZNF51 LAZ3 ]
  • Gene: [03q27/DVL3] dishevelled 3 (homologous to Drosophila dsh);
  • Gene: [03q27/EHHADH] 3-hydroxyacyl Coenzyme A dehydrogenase (EC:1.1.1.35); enoyl-Coenzyme A, hydratase (EC:4.2.1.17); 3,2-trans-enoyl-Coenzyme A isomerase (EC:5.3.3.8);
  • Gene: [03q27/EIF4G1] eukaryotic translation initiation factor 4 gamma 1; [EIF4F ]
  • Gene: [03q27/FIM3] friend-murine leukemia virus integration site 3 homolog;
  • Gene: [03q27/FRA3C] fragile site 3q27, aphidicolin type, common;
  • Gene: [03q27/HRG] histidine-rich glycoprotein (plasminogen/heparin-binding); thrombophilia due to elevated HRG;
  • Gene: [03q27/KNG] kininogen (alpha-2-thiol proteinase inhibitor; contains bradykinin); Williams trait (total kininogen deficiency); [BDK ]
  • Gene: [03q27/RFC4] replication factor C (activator 1) 4 (37kD);
  • Gene: [03q27/THPO] thrombopoietin (megkaryocyte colony stimulating factor); megakaryocyte growth and development factor; myeloproliferative leukemia virus oncogene ligand; myeloproliferative leukemia; [TPO MGDF MPLL ]
  • Gene: [03q28/CLAPM1] clathrin-associated/assembly/adaptor protein, medium 1 (50kD); clathrin adaptor protein 50; [AP50 ]
  • Gene: [03q28/ETV5] ets translocation variant gene 5 (ets-related molecule); [ERM ETV2L1 ]
  • Gene: [03q28/FGF12] fibroblast growth factor 12; [FHF1 ]
  • Gene: [03q28/IL1RAP] interleukin 1 receptor accessory protein; [IL-1RAcP ]
  • Gene: [03q28/NDUFS8] NADH dehydrogenase (ubiquinone) Fe-S protein 8 (23kD; NADH-CoQ reductase; EC:1.6.5.3, EC:1.6.99.3);
  • Gene: [03q28/SST] somatostatin (preprosomatostatin); growth hormone release-inhibiting hormone (somatostatin);
  • Gene: [03q29/DLG1] discs, large (Drosophila) homolog 1;
  • Gene: [03q29/MUC4] mucin 4, tracheobronchial;
  • Gene: [03q29/PPP1R2] protein phosphatase 1, regulatory (inhibitor) subunit 2;
  • Gene: [03q29/RPL29] ribosomal protein L29 (cell surface heparin binding protein); heparin/heparan sulfate interacting protein; [HIP ]
  • Gene: [03q29/RPL35A] ribosomal protein L35a;
  • Gene: [03q29/TFRC] transferrin receptor (protein p90; antigen CD71, MFI2); [OKT9 MAP97 ]
  • Gene: [03^/ACTGP1] actin, gamma pseudogene 1;
  • Gene: [03^/ACTL4] actin-like sequence 4;
  • Gene: [03^/AF8T] temperature sensitivity complementing AF8 mutation; [CCCG1 ]
  • Gene: [03^/ALDOAP1] aldolase A, fructose-bisphosphate pseudogene 1;
  • Gene: [03^/CRYGS] crystallin, gamma S polypeptide; [CRYG8 ]
  • Gene: [03^/D3Z1] alphoid satellite DNA from chr 3 (probe pHS05);
  • Gene: [03^/DEM] dementia, familial non-specific;
  • Gene: [03^/DHFRP4] dihydrofolate reductase pseudogene 4;
  • Gene: [03^/ERCM1] excision repair complementing in mouse cells; excision repair complementing defective repair in mouse cells;
  • Gene: [03^/ERVT4] endogenous retroviral sequence, truncated 4 (band T4, 14.9 kb);
  • Gene: [03^/GP9] glycoprotein IX (platelet);
  • Gene: [03^/GSTM1L] glutathione S-transferase M1-like;
  • Gene: [03^/HPRTP1] hypoxanthine phosphoribosyltransferase pseudogene 1;
  • Gene: [03^/HSPBL1] heat shock 27kD protein-like 1;
  • Gene: [03^/P2RY1] purinergic receptor P2Y, G-protein coupled, 1 (purinoceptor P2Y1); [P2Y1 ]
  • Gene: [03^/PANG] plasmacytoma-associated neuronal glycoprotein;
  • Gene: [03^/PDHB] pyruvate dehydrogenase, E1 beta polypeptide;
  • Gene: [03^/PLS1] plastin 1 (I isoform, intestine specific);
  • Gene: [03^/PPIP6] peptidylprolyl cis-trans-isomerase (cyclophilin) pseudogene 6;
  • Gene: [03^/PRKCD] protein kinase C, delta polypeptide;
  • Gene: [03^/PROS1] protein S, alpha (activated protein-C cofactor; vitamin K-dependent); thromboembolic disease, recurrent venous; [PROS ]
  • Gene: [03^/PROSP] protein S, beta (pseudogene); [PROS2 ]
  • Gene: [03^/PTK8] protein tyrosine kinase PTK8;
  • Gene: [03^/QARS] glutaminyl-tRNA synthetase;
  • Gene: [03^/RPS6KA1] ribosomal protein S6 kinase, 90kD, polypeptide A1;
  • Gene: [03^/SRML2] spermidine synthase-like 2;
  • Gene: [03^/SYN2] synapsin II;
  • Gene: [03^/TFP] transferrin, pseudogene;
  • Gene: [03^/TRH] thyrotropin-releasing hormone;
  • Gene: [03^/ZNF80] zinc finger protein 80 (pT17);
  • Gene: [04p1/ADRA2C] adrenergic, alpha-2C-, receptor; [ADRA2RL2 ]
  • Gene: [04p1/ART3] ADP-ribosyltransferase 3, testis;
  • Gene: [04p1/CNGA1] cyclic nucleotide gated channel alpha 1; cyclic nucleotide gated channel (photoreceptor), cGMP gated 1 (alpha); retinal rod cGMP-gated channel, alpha subunit (63kD); retinitis pigmentosa, autosomal recessive (CNGA1 gene m
  • Gene: [04p1/DPYSL1] dihydropyrimidinase-like 1; collapsin response mediator protein 1; [DRP-1 CRMP1 ]
  • Gene: [04p1/GABRA2] gamma-aminobutyric acid (GABA) A receptor, alpha 2;
  • Gene: [04p1/GABRB1] gamma-aminobutyric acid (GABA) A receptor, beta 1;
  • Gene: [04p1/LDHAL1] lactate dehydrogenase A-like 1;
  • Gene: [04p1/RFC1] replication factor C (activator 1) 1 (145kD);
  • Gene: [04p1/RPL9] ribosomal protein L9;
  • Gene: [04p12/PTK4] protein tyrosine kinase PTK4;
  • Gene: [04p12/TEC] protein tyrosine kinase TEC, non-receptor;
  • Gene: [04p12/TXK] protein tyrosine kinase TXK, non-receptor;
  • Gene: [04p14/HIP2] huntingtin interacting protein 2; ubiquitin-conjugating enzyme E2 (25kD);
  • Gene: [04p14/TIL] Toll/interleukin-1 receptor-like; Toll (Drosophila) homolog; [KIAA0012 ]
  • Gene: [04p14/UCHL1] ubiquitin carboxyl-terminal esterase L1 (neuron-specific);
  • Gene: [04p15/CD38] antigen CD38 (p45; monoclonal antibody OKT-10); ADP-ribosyl cyclase/cyclic ADP-ribose hydrolase; diabetes mellitus 2, association with;
  • Gene: [04p15/DRD5] dopamine receptor D5; dopamine receptor D1B (MIM:126448); [DRD1L2 DRD1B ]
  • Gene: [04p15/FRA4D] fragile site 4p15, aphidicolin type, common;
  • Gene: [04p15/PCDH7] protocadherin 7 (brain-heart); [BHPCDH ]
  • Gene: [04p153/ACOX3] acyl-Coenzyme A oxidase 3, pristanoyl, peroxisomal;
  • Gene: [04p153/QDPR] quinoid dihydropteridine reductase; phenylketonuria II, atypical (QDPR/DHPR deficiency);
  • Gene: [04p16/CRS3] craniosynostosis, Adelaide type; [CRSA ]
  • Gene: [04p16/CTBP1] C-terminal binding protein 1;
  • Gene: [04p16/EVC] Ellis-van Creveld syndrome (6-fingered dwarfism); chondroectodermal dysplasia (mesoectodermal dysplasia);
  • Gene: [04p16/GAK] cyclin G associated kinase;
  • Gene: [04p16/S100P] S100 calcium-binding protein P;
  • Gene: [04p161/FRA4A] fragile site 4p16.1, aphidicolin type, common;
  • Gene: [04p161/HMX1] homeo box (H6 family) 1;
  • Gene: [04p161/MSX1] msh (Drosophila) homeo box homolog 1 (homeo box 7); homeo box (H7 family) 1; [WHS WHCR HOX7 ]
  • Gene: [04p161/NKX3B] NK homeobox (Drosophila), family 3, B; bagpipe homeobox (Drosophila) homolog 1; [NKX3.2 Bapx1 ]
  • Gene: [04p161/RAF1P1] murine leukemia viral oncogene pseudogene 1 (oncogene raf-2?); [RAF2 ]
  • Gene: [04p161/WFS] diabetes mellitus and insipidus with optic atrophy and deafness (Wolfram syndrome); [DIDMOAD ]
  • Gene: [04p162/ASVS1] adenovirus/SV40 integration site 1;
  • Gene: [04p163/ADD1] adducin 1 (alpha); [ADDA ]
  • Gene: [04p163/D4S10] DNA segment G8 (Huntigton disease DNA-marker);
  • Gene: [04p163/DFNA6] deafness, autosomal dominant 6;
  • Gene: [04p163/DGKQ] diacylglycerol kinase, theta (110kD);
  • Gene: [04p163/FGFR3] fibroblast growth factor receptor 3; protein tyrosine kinase FGFR-like 3; achondroplasia (MIM:100800); Muenke nonsyndromic coronal craniosynostosis (MIM:602849); thanatophoric dysplasia (MIM:187600);
  • Gene: [04p163/GPRK2L] G protein-coupled receptor kinase 2 (Drosophila)-like;
  • Gene: [04p163/HBP] hairpin binding protein, histone (stem-loop binding protein); [SLBP ]
  • Gene: [04p163/HD] huntingtin (HD protein); Huntington disease;
  • Gene: [04p163/IDUA] alpha-L-iduronidase; mucopolysaccharidosis I (Hurler/Scheie syndromes; alpha-L-iduronidase deficiency);
  • Gene: [04p163/LRPAP1] low density lipoprotein receptor-related protein-associated protein 1; alpha-2-macroglobulin receptor-associated protein; [A2MRAP ]
  • Gene: [04p163/MYL5] myosin, light polypeptide 5, regulatory;
  • Gene: [04p163/PDE6B] phosphodiesterase 6B, cGMP-specific, rod, beta; retinal rod photoreceptor cGMP phosphodiesterase, beta subunit; retinitis pigmentosa (cGMP phosphodiesterase 6B deficiency); congenital stationary night blindness 3 (hemer
  • Gene: [04p163/RGS12] regulator of G-protein signalling 12;
  • Gene: [04p163/RNF4] ring finger protein 4;
  • Gene: [04p163/SH3BP2] SH3 domain binding protein 2;
  • Gene: [04p163/WHCR] Wolf-Hirschhorn syndrome candidate 1; Wolf-Hirschhorn syndrome (MIM:194190); [WHS WHSC1 ]
  • Gene: [04p163/ZNF141] zinc finger protein 141 (clone pHZ-44);
  • Gene: [04q/AGA] aspartyl-beta-glucosaminidase; aspartylglycosaminuria;
  • Gene: [04q/ANX2P1] annexin II (lipocortin II) pseudogene 1; [LPC2A ANX2L1 ]
  • Gene: [04q/AREG] amphiregulin; schwannoma-derived growth factor; [SDGF ]
  • Gene: [04q/ASMD] anterior segment mesenchymal dysgenesis; [ASOD ]
  • Gene: [04q/ASSP8] argininosuccinate synthetase pseudogene 8;
  • Gene: [04q/BTC] betacellulin;
  • Gene: [04q/CCNA] cyclin A (G2/mitotic specific); [CCN1 ]
  • Gene: [04q/CLGN] calmegin;
  • Gene: [04q/CLTB] clathrin, light polypeptide (Lcb);
  • Gene: [04q/COX5BL1] cytochrome c oxidase subunit Vb-like 1;
  • Gene: [04q/DCK] deoxycytidine kinase;
  • Gene: [04q/FAB2] fatty acid binding protein 2, intestinal; insulin resistance? (fat transport diturbance?); [FABP2 ]
  • Gene: [04q/GSTMS2] glutathione S-transferase, microsomal, 2;
  • Gene: [04q/GYPA] glycophorin A (MN blood group); [MNS MN ]
  • Gene: [04q/GYPB] glycophorin B (SS blood group);
  • Gene: [04q/GYPE] glycophorin E;
  • Gene: [04q/HCL2] hair color 2 (red); [RHC ]
  • Gene: [04q/IFNB4] interferon, beta 4, fibroblast;
  • Gene: [04q/IL8] interleukin 8 (monocyte-derived neutrophil chemotactic factor); [MDNCF ]
  • Gene: [04q/M4S1] membrane component, chromosome 4, surface marker 1 (35kD glycoprotein); gastrointestinal tumor-associated antigen 2 (35kD; identified by monoclonal antibody GA733); [KSA ]
  • Gene: [04q/MLT2P] metallothionein 2 pseudogene 1 (processed); [MT2P1 ]
  • Gene: [04q/MUC7] mucin 7, salivary;
  • Gene: [04q/PEE1] preeclampsia/eclampsia 1 (gestational proteinuric hypertension);
  • Gene: [04q/PF4V1] platelet factor 4 variant 1;
  • Gene: [04q/PF4] platelet factor 4;
  • Gene: [04q/PRKG2] protein kinase, cGMP-dependent, type II; [cGKII PRKGR2 ]
  • Gene: [04q/RRH] peropsin, visual pigment-like receptor;
  • Gene: [04q/SCYB5] small inducible cytokine B5 (epithelial-derived neutrophil-activating peptide 78); [ENA-78 ]
  • Gene: [04q/SF] Stoltzfus blood group;
  • Gene: [04q/TYS] sclerotylosis (scleroatrophic and keratotic dermatosis of limbs);
  • Gene: [04q1/AFM] afamin (alpha-albumin); [ALBA ALB2 ]
  • Gene: [04q1/AFP] alpha-fetoprotein; hereditary persistence of alpha-fetoprotein (HPAFP); [HPAFP ]
  • Gene: [04q1/AIH2] amelogenesis imperfecta 2, hypocalcification (autosomal dominant);
  • Gene: [04q1/ALB] albumin (alloalbuminemia familial, asymptomatic); dysalbuminemic hyperthyroxinemia, familial; analbuminemia congenital; hyperzincemia, familial dysalbuminemic (MIM:194470); [FDH ]
  • Gene: [04q1/CENPC1] centromere protein C (autoantigen C; 140kD);
  • Gene: [04q1/DGI] dentinogenesis imperfecta 1; [DGI1 ]
  • Gene: [04q1/GC] group-specific component (vitamin D binding protein); vitamin D binding protein (group-specific component); [DBP VDBG ]
  • Gene: [04q1/JPD] periodontitis, juvenile; [JP AP ]
  • Gene: [04q1/PPBPL1] pro-platelet basic protein (beta-thromboglobulin)-like 1; neutrophil-activating peptide-2-like 1;
  • Gene: [04q1/PPBP] pro-platelet basic protein (beta-thromboglobulin); neutrophil-activating peptide-2 (connective tissue-activating peptide III); [THBGB1 TGB1 ]
  • Gene: [04q1/STATH] statherin (salivary protein); [STR SPFSTAT ]
  • Gene: [04q12/FRA4B] fragile site 4q12, BrdU type, common;
  • Gene: [04q12/GCSPP] glycine cleavage system protein P, processed pseudogene; glycine dehydrogenase (decarboxylating), processed pseudogene; glycine decarboxylase, processed pseudogene; [GLDCP ]
  • Gene: [04q12/IGFB7] insulin-like growth factor binding protein 7; [PSF MAC25 ]
  • Gene: [04q12/KDR] tyrosine kinase growth factor receptor (KDR; kinase insert domain receptor); growth factor receptor tyrosine kinase; vascular endothelial growth factor receptor (FLK1);
  • Gene: [04q12/KIT] protooncogene tyrosine protein kinase KIT (CD117); v-kit Hardy-Zuckerman 4 feline sarkoma virus homolog; piebald trait (piebaldism; MIM:172800); mast/stem cell growth factor receptor; mast cell leukemia (mastocytosis with
  • Gene: [04q12/PAICS] phosphoribosylaminoimidazole carboxylase (AIR carboxylase; EC:4.1.1.21); phosphoribosylaminoimidazole succinocarboxamide synthetase (SAICAR synthetase; EC:6.3.2.6);
  • Gene: [04q12/PDGFRA] platelet-derived growth factor receptor, alpha polypeptide;
  • Gene: [04q12/POLR2B] RNA polymerase II (DNA directed) polypeptide B (140kD);
  • Gene: [04q12/PPAT] phosphoribosyl pyrophosphate amidotransferase;
  • Gene: [04q12/SGCB] sarcoglycan, beta (dystrophin-associated glycoprotein, 43kD); limb girdle muscular dystrophy 2E (autosomal recessive); [SGC LGMD2E ]
  • Gene: [04q12/TAPVR1] total anomalous pulmonary venous return 1;
  • Gene: [04q13/GKP2] glycerol kinase pseudogene 2;
  • Gene: [04q13/GRSF1] G-rich RNA sequence binding factor 1;
  • Gene: [04q13/HTN1] histatin 1 (histidine rich salivary protein 1); salivary protein, histatin 1 (histidine rich); [HIS1 SPFHTN1 ]
  • Gene: [04q13/HTN3] histatin 3 (histidine rich salivary protein 3); [HTN2 SPFHTN3 ]
  • Gene: [04q13/TYRO4] protein tyrosine kinase TYRO4;
  • Gene: [04q13/UGT2B10] UDP-glucuronosyltransferase 2 family, polypeptide B, gene 10;
  • Gene: [04q13/UGT2B15] UDP-glucuronosyltransferase 2 family, polypeptide B, gene 15;
  • Gene: [04q13/UGT2B4] UDP-glucuronosyltransferase 2 family, polypeptide B, gene 4;
  • Gene: [04q13/UGT2B7] UDP-glucuronosyltransferase 2 family, polypeptide B, gene 7;
  • Gene: [04q131/STE] sulfotransferase, estrogen-preferring;
  • Gene: [04q2/ADH7] alcohol dehydrogenase 7 (class IV), sigma polypeptide;
  • Gene: [04q2/ANK2] ankyrin 2, neuronal (ankyrin B);
  • Gene: [04q2/ANX5] annexin V (lipocortin V; endonexin II; calphobindin I); placental anticoagulant protein I (vascular anticoagulant, alpha); thromboplastin inhibitor; [ENX2 PAP1 ]
  • Gene: [04q2/CASP6] caspase 6, apoptosis-related cysteine protease;
  • Gene: [04q2/CENPE] centromere protein E (autoantigen E; 312kD);
  • Gene: [04q2/EIF4E] eukaryotic translation initiation factor 4E; eukaryotic translation initiation factor 4E-like 1;
  • Gene: [04q2/FDH] formaldehyde dehydgogenase;
  • Gene: [04q2/GNPTA] UDP-N-acetylglucosaminyl-phosphotransferase; mucolipidoses II/III (I cell desease); pseudo-Hurler polydystrophy (MIM:252600; mucolipidosis III);
  • Gene: [04q2/HADHSC] L-3-hydroxyacyl-CoA dehydrogenase, short-chain; SCHAD deficiency;
  • Gene: [04q2/HSPCP1] heat shock 90kD protein pseudogene 1;
  • Gene: [04q2/IBSP] integrin-binding sialoprotein (bone sialoprotein II);
  • Gene: [04q2/IL2] interleukin 2 (T-cell growth factor); [TCGF ]
  • Gene: [04q2/LEF1] lymphoid enhancer-binding factor 1;
  • Gene: [04q2/LQT4] long (electrocardiographic) QT syndrome 4;
  • Gene: [04q2/MANBA] mannosidase, beta A, lysosomal; mannosidosis, beta- (lysosomal beta-mannosidase deficiency);
  • Gene: [04q2/NKX6A] NK homeobox (Drosophila), family 6, member A;
  • Gene: [04q2/PDHA2] pyruvate dehydrogenase, E1 alpha polypeptide 2 (testicular);
  • Gene: [04q2/PKD2] polycystin 2; polycystic kidney disease, adult, type 2 (autosomal dominant); [ARPKD ]
  • Gene: [04q2/PPP3CA] protein phosphatase 3 (formerly 2B), catalytic subunit, alpha isoform; calcineurin A alpha;
  • Gene: [04q2/RAP1GDS1] RAP1, GTP-GDP dissociation stimulator 1;
  • Gene: [04q2/SNCA] synuclein, alpha (non A4 component of amyloid precursor); Parkinson disease, familial 1 (MIM:601508); [NACP PD1 ]
  • Gene: [04q2/SPP1] secreted phosphoprotein 1 (osteopontin, bone sialoprotein I, early T-lymphocyte activation 1); [OPN BNSP ]
  • Gene: [04q21/AMBN] ameloblastin, enamel matrix protein;
  • Gene: [04q21/ANX3] annexin III (lipocortin III); 1,2-cyclic-inositol-phosphate phosphodiesterase; placental anticoagulant protein III (calcimedin 35-alpha);
  • Gene: [04q21/AUF1A] AU-rich element RNA-binding protein 1A, 37kD; [AUF1 ]
  • Gene: [04q21/DMP1] dentin matrix acidic phosphoprotein;
  • Gene: [04q21/FGF5] fibroblast growth factor 5 (fgf.5 oncogene);
  • Gene: [04q21/GRO1] oncogene GRO1 (GRO-alpha; melanoma growth stimulating activity); neutrophil-activating protein 3; [GRO NAP3 MGSA ]
  • Gene: [04q21/GRO2] oncogene GRO2 (GRO-beta); macrophage inflammatory protein Mip2-alpha; [MIP2A ]
  • Gene: [04q21/GRO3] oncogene GRO3 (GRO-gamma); macrophage inflammatory protein Mip2-beta; [MIP2B ]
  • Gene: [04q21/IFNI10] interferon-inducible cytokine IP-10; interferon, gamma-inducible protein 10; [INP10 IP10 IF ]
  • Gene: [04q21/IGJ] immunoglobulin, J linker protein for alpha/mu subunits; [JCH ]
  • Gene: [04q21/MIG] monokine induced by gamma interferon; chemokine; [CMK ]
  • Gene: [04q21/MLLT2] myeloid/lymphoid or mixed-lineage leukemia (trithorax (Drosophila) homolog); translocated to, 2; [AF4 ]
  • Gene: [04q21/PTPN13] protein tyrosine phosphatase, non-receptor type 13;
  • Gene: [04q21/SCYB6] small inducible cytokine subfamily B (Cys-X-Cys), member 6; granulocyte chemotactic protein 2; [GCP2 ]
  • Gene: [04q211/CSN10] casein, kappa; [CSN3 CASK ]
  • Gene: [04q211/CSN1] casein, alpha 1; [CASA ]
  • Gene: [04q211/CSN2] casein, beta; [CASB ]
  • Gene: [04q212/GNRHR] gonadotropin-releasing hormone receptor; leutinizing hormone-releasing hormone receptor;
  • Gene: [04q22/ADH1] alcohol dehydrogenase 1 (class I), alpha polypeptide;
  • Gene: [04q22/ADH2] alcohol dehydrogenase 2 (class I), beta polypeptide;
  • Gene: [04q22/ADH3] alcohol dehydrogenase 3 (class I), gamma polypeptide;
  • Gene: [04q22/ADH4] alcohol dehydrogenase 4 (class II), pi polypeptide;
  • Gene: [04q22/ADH5P1] alcohol dehydrogenase 5 (class III), chi polypeptide pseudogene 1;
  • Gene: [04q22/ADH5] alcohol dehydrogenase 5 (class III), chi polypeptide (EC:1.1.1.1); glutathione-dependent formaldehyde dehydrogenase (EC:1.2.1.1);
  • Gene: [04q22/ATOH1] atonal (Drosophila) homolog 1; [HATH1 ]
  • Gene: [04q22/GRID2] glutamate receptor, ionotropic, delta 2;
  • Gene: [04q24/H2AZ] histone H2AZ (basal);
  • Gene: [04q24/MTP] microsomal triglyceride transfer protein, large polypeptide (88kD); abetalipoproteinemia (acanthocytosis; MIM:200100);
  • Gene: [04q24/NFKB1] nuclear factor of kappa light chain gene enhancer in B-cells 1 (p105); transcription factor kappa-B, subunit 1 (p105);
  • Gene: [04q25/EGF] epidermal growth factor; urogastrone (MIM:191810); [URG ]
  • Gene: [04q25/FGF2] fibroblast growth factor 2 (basic; angiogenesis stimulator); prostatropin; [HBGF2 FGFB ]
  • Gene: [04q25/IF] complement component I (C3b/C4b inactivator); I factor (complement); complement component I deficiency (C3b/C4b inactivator deficiency);
  • Gene: [04q25/PITX2] pituitary homeo box 2; bicoid-related homeobox transcription factor (solurshin); Rieger syndrome 1 (MIM:180500); iridogoniodysgenesis, type 2 (MIM:137600); iris hypoplasia with glaucoma 2; [PTX2 RIEG1 ]
  • Gene: [04q26/UGT8] UDP glycosyltransferase 8; UDP-galactose-ceramide galactosyltransferase;
  • Gene: [04q27/FRA4E] fragile site 4q27, unclassified type, common;
  • Gene: [04q28/F1A] fibrinogen, alpha polypeptide; dysfibrinogenemia-alpha; afibrinogenemia; amyloidosis VIII (systemic nonneuropathic, Ostertag type, German type; MIM:105200); [FGA ]
  • Gene: [04q28/F1B] fibrinogen, beta polypeptide; dysfibrinogenemia-beta; [FGB ]
  • Gene: [04q28/F1G] fibrinogen, gamma polypeptide; dysfibrinogenemia-gamma; [FGG ]
  • Gene: [04q28/MADH1] MAD (mothers against decapentaplegic, Drosophila) homolog 1; [SMAD1 JV4-1 ]
  • Gene: [04q3/CLCN3] chloride channel 3;
  • Gene: [04q3/COX7A2] cytochrome c oxidase subunit VIIa polypeptide 2 (liver);
  • Gene: [04q3/ETFDH] electron-transferring-flavoprotein dehydrogenase; glutaricaciduria IIC (ETF dehydrogenase deficiency);
  • Gene: [04q3/FACL2] fatty-acid-CoA ligase, long-chain 2; palmitoyl-CoA ligase 2;
  • Gene: [04q3/FAT] FAT tumor suppressor (Drosophila) homolog;
  • Gene: [04q3/GRIA2] glutamate receptor, ionotropic, AMPA 2; [GLUR2 ]
  • Gene: [04q3/HPGD] hydroxyprostaglandin dehydrogenase 15-(NAD);
  • Gene: [04q3/NPY1R] neuropeptide Y receptor Y1; [NPYR ]
  • Gene: [04q3/NPY5R] neuropeptide Y receptor Y5;
  • Gene: [04q3/PLRG1] pleiotropic regulator 1 (PRL1, Arabidopsis thaliana homolog); [PRL1 ]
  • Gene: [04q3/SC4MOL] sterol-C4-methyl oxidase-like;
  • Gene: [04q31/GTF2F2L] general transcription factor IIF, polypeptide 2-like;
  • Gene: [04q31/HMG2] high-mobility group (nonhistone chromosomal) protein 2;
  • Gene: [04q31/IL15] interleukin 15;
  • Gene: [04q31/NPY2R] neuropeptide Y receptor Y2;
  • Gene: [04q31/RNASELI] ribonuclease L (2',5'-oligoisoadenylate synthetase-dependent) inhibitor; [RNS4I ]
  • Gene: [04q31/RPS3A] ribosomal protein S3a; mitochondrial fusion target-like; [MFTL MPTL ]
  • Gene: [04q31/TDO2] tryptophan 2,3-dioxygenase (tryptophan oxygenase);
  • Gene: [04q31/UCP1] uncoupling protein 1 (mitochondrial, proton carrier); brown adipose tissue uncoupling protein (thermogenin);
  • Gene: [04q311/FRA4C] fragile site 4q31.1, aphidicolin type, common;
  • Gene: [04q312/MLR] mineralocorticoid receptor (aldosterone receptor); pseudohypoaldosteronism, type I, autosomal dominant (MIM:177735); [MCR ]
  • Gene: [04q312/POU4F2] POU domain, class 4, transcription factor 2; [BRN3B ]
  • Gene: [04q32/GKP3] glycerol kinase pseudogene 3;
  • Gene: [04q32/GLRB] glycine receptor, beta;
  • Gene: [04q32/GUCY1A3] guanylate cyclase 1, soluble, alpha 3 (82kD);
  • Gene: [04q32/GUCY1B3] guanylate cyclase 1, soluble, beta 3 (70kD);
  • Gene: [04q321/HVBS6] hepatitis B virus integration site 6 (hepatocarcinoma); hepatocarcinoma (hepatitis B virus integration site 6); [D4S122 HCC2 ]
  • Gene: [04q34/CASP3] caspase 3, apoptosis-related cysteine protease; apopain (PARP cleavage protease);
  • Gene: [04q34/GPM6A] glycoprotein M6A (neuronal?); [GPM6 ]
  • Gene: [04q35/ANT1] adenine nucleotide translocator 1 (skeletal muscle);
  • Gene: [04q35/F11] coagulation factor XI (plasma thromboplastin antecedent); hypothromboplastinemia (Rosenthal syndrome, coagulation factor XI deficiency);
  • Gene: [04q35/FRG1] FSHD region gene 1;
  • Gene: [04q35/FSHMD1A] facioscapulohumeral muscular dystrophy 1A, Landouzy-Dejerine; [FSHD FMD ]
  • Gene: [04q35/HSPCAL2] heat shock 90kD protein, alpha-like 2;
  • Gene: [04q35/KLK3] kallikrein 3, plasma (Fletcher factor); Fletcher factor deficiency (plasma kallikrein deficiency);
  • Gene: [04q351/IRF2] interferon regulatory factor 2 (repressor);
  • Gene: [04q351/MTNR1A] melatonin receptor 1A;
  • Gene: [04^/ATP1BL1] ATPase, Na+,K+ transporting, beta polypeptide-like 1;
  • Gene: [04^/BMP3] bone morphogenetic protein 3 (osteogenin);
  • Gene: [04^/CCKAR] cholecystokinin A receptor;
  • Gene: [04^/CD36L2] antigen CD36 (collagen type I receptor, thrombospondin receptor)-like 2; lysosomal integral membrane protein II (85kD); [LIMPII ]
  • Gene: [04^/CPE] carboxypeptidase E (carboxypeptidase H; enkephalin convertase);
  • Gene: [04^/DSPP] dentin sialophosphoprotein;
  • Gene: [04^/EDNRA] endothelin receptor type A (endothelin 1 receptor);
  • Gene: [04^/GABRA4] gamma-aminobutyric acid (GABA) A receptor, alpha 4;
  • Gene: [04^/GABRG1] gamma-aminobutyric acid (GABA) A receptor, gamma 1;
  • Gene: [04^/GAPDL4] glyceraldehyde-3-phosphate dehydrogenase-like 4;
  • Gene: [04^/GTA] galactosyltransferase activator; glycoprotein-4-beta-galactosyltransferase activator; [GGTB1 ]
  • Gene: [04^/LAG5] leukocyte antigen group 5 (granulocytic); neutropenia, autoimmune/alloimmune neonatal;
  • Gene: [04^/MDF1] antigen MDF1 (monoclonal antibody A-3A4);
  • Gene: [04^/PDE1A] phosphodiesterase 1A, calcium/calmodulin-dependent (61kD);
  • Gene: [04^/PEPS] peptidase S;
  • Gene: [04^/PGM2] phosphoglucomutase 2;
  • Gene: [04^/PPEF2] protein phosphatase, EF hand calcium-binding domain 2;
  • Gene: [04^/PPID] peptidylprolyl cis-trans-isomerase D (cyclophilin D; rotamase);
  • Gene: [04^/SEN1] senescence (cellular)-related 1; [SEN ]
  • Gene: [04^/SOD3] superoxide dismutase 3, extracellular;
  • Gene: [04^/SPINK2] serine protease inhibitor, Kazal type 2 (acrosin-trypsin inhibitor);
  • Gene: [04^/SRIL] sorcin-like;
  • Gene: [04^/TMSL3] thymosin-like 3;
  • Gene: [04^/TS13] temperature sensitivity complementation, TS-13;
  • Gene: [05p1/AVRR] antiviral state repressor regulator;
  • Gene: [05p1/CDH12] cadherin 12 (N-cadherin 2; Br-cadherin);
  • Gene: [05p1/CMDJ] craniometaphyseal dysplasia, Jackson type (dominant);
  • Gene: [05p1/FGF10] fibroblast growth factor 10;
  • Gene: [05p1/GDNF] glial cell line derived neurotrophic factor; Hirschsprung disease (MIM:142623); [HSCR ]
  • Gene: [05p1/GHR] growth hormone receptor; pituitary dwarfism II (Laron type; MIM:262500); [GHBP LTD LS ]
  • Gene: [05p1/HMGCS1] 3-hydroxy-3-methylglutaryl-Coenzyme A synthase 1 (soluble);
  • Gene: [05p1/HPRTP2] hypoxanthine phosphoribosyltransferase pseudogene 2;
  • Gene: [05p1/LIFR] leukemia inhibitory factor receptor;
  • Gene: [05p1/MHS6] malignant hyperthermia susceptibility 6;
  • Gene: [05p1/MYO10] myosin X;
  • Gene: [05p1/NNT] nicotinamide nucleotide transhydrogenase (NAD(P)+);
  • Gene: [05p1/NPR3] natriuretic peptide receptor C; [ANPRC NPRC AN ]
  • Gene: [05p1/PRLR] prolactin receptor;
  • Gene: [05p1/TARS] threonyl-tRNA synthetase;
  • Gene: [05p1/TRIO] triple functional domain (PTPRF interacting);
  • Gene: [05p1/ZNF131] zinc finger protein 131 (clone pHZ-10);
  • Gene: [05p1/ZNF4] zinc finger protein 4 (probe 5CMP1); [TZF1 ]
  • Gene: [05p12/PRKAA1] protein kinase, AMP-activated, alpha 1 catalytic subunit (AMPK alpha 1);
  • Gene: [05p13/C6] complement component 6;
  • Gene: [05p13/C7] complement component 7; complement component 7 deficiency;
  • Gene: [05p13/C9] complement component 9; complement component 9 deficiency;
  • Gene: [05p13/DOC2] differentially expressed in ovarian cancer 2;
  • Gene: [05p13/FRA5A] fragile site 5p13, BrdU type, common;
  • Gene: [05p13/IL7R] interleukin 7 receptor (antigen CDW127);
  • Gene: [05p13/OXCT] 3-oxoacid CoA transferase (succinyl CoA:); ketoacidosis of infancy (succinyl CoA: 3-oxoacid CoA transferase deficiency);