Gene: [04q2/SNCA] synuclein, alpha (non A4 component of amyloid precursor); Parkinson disease, familial 1 (MIM:601508); [NACP PD1 ] — Gene: [06p2/H4FK] H4 histone family, member K; [H4/k ]

  • 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);
  • Gene: [05p13/SKP2] S-phase kinase-associated protein 2 (p45); CDK2/cyclin A-associated protein p45;
  • Gene: [05p13/SLC1A3] solute carrier family 1 (glial high affinity glutamate transporter), member 3; [EAAT1 GLAST ]
  • Gene: [05p131/PTGER2] prostaglandin E2 receptor 2 (subtype EP2), 53kD;
  • Gene: [05p14/FRA5E] fragile site 5p14, aphidicolin type, common;
  • Gene: [05p14/MLVI2] Moloney murine leukemia virus (MoMuLV) integration site 2 homolog; [MLV12 ]
  • Gene: [05p14/PMCHL1] pro-melanin-concentrating hormone-like 1;
  • Gene: [05p15/ADCY2] adenylate cyclase 2 (brain);
  • Gene: [05p15/MTRR] 5-methyltetrahydrofolate-homocysteine methyltransferase reductase; methionine synthase reductase; homocystinuria-megaloblastic anemia (due to defect in cobalamin metabolism; MIM:236270);
  • Gene: [05p15/SDHA] succinate dehydrogenase complex, subunit A, flavoprotein (Fp) subunit; Leigh syndrome (succinate dehydrogenase deficiency);
  • Gene: [05p15/SRD5A1] steroid-5-alpha-reductase, alpha polypeptide 1; pseudohermaphroditism, male (steroid-5-alpha-reductase alpha 1 deficiency);
  • Gene: [05p152/DAP1] death-associated protein 1; [DAP ]
  • Gene: [05p153/SLC6A3] solute carrier family 6 (neurotransmitter transporter, dopamine), member 3; [DAT1 ]
  • Gene: [05p153/SLC9A3] solute carrier family 9 (sodium/hydrogen exchanger), isoform 3; [NHE3 ]
  • Gene: [05p1533/TERT] telomerase reverse transcriptase;
  • Gene: [05q/CAST] calpastatin (calpain inhibitor);
  • Gene: [05q/CCAL1] chondrocalcinosis 1; [CCAL2 ]
  • Gene: [05q/CCA] congenital contractural arachnodactyly (Marfanoid-like);
  • Gene: [05q/CD14] antigen CD14 (monoclonal antibodies MO2, MY4, LEUM3); monocyte differentiation antigen CD14;
  • Gene: [05q/CHD1] chromodomain helicase DNA binding protein 1;
  • Gene: [05q/CRHBP] corticotropin releasing hormone-binding protein;
  • Gene: [05q/EGR1] early growth response 1 (transcription factor Krox24-like); zinc-finger protein EGR1 (early growth response 1; Krox24-like); [KROX24]
  • Gene: [05q/FAB6] fatty acid binding protein 6, ileal (gastrotropin); gastrotropin (ileal lipid-binding protein; 15kD); [FABP6 ILBP ]
  • Gene: [05q/FBN2] fibrillin 2;
  • Gene: [05q/ISL1] ISL1 transcription factor, LIM/homeodomain (islet 1); insulin gene enhancer protein ISL-1;
  • Gene: [05q/ITGA2] integrin, alpha 2 (antigen CD49B, alpha 2 subunit of VLA-2 receptor); very late activation protein-2 receptor, alpha-2 subunit; glicoprotein Ia; [CD49B VLA2R ]
  • Gene: [05q/LMNB1] lamin B1;
  • Gene: [05q/LOX] lysyl oxidase;
  • Gene: [05q/NEUROD3] neurogenic differentiation 3;
  • Gene: [05q/NME5] non-metastatic cells 5, protein expressed in; nucleoside diphosphate kinase NME5;
  • Gene: [05q/PAM] peptidylglycine alpha-amidating monooxygenase;
  • Gene: [05q/PCSK1] proprotein convertase subtilisin/kexin-like type 1; neuroendocrine convertase 1 (proprotein convertase PC1); obesity and endocrinopathy due to impaired prohormone processing (MIM:600955);
  • Gene: [05q/PPP2CA] protein phosphatase 2 (formerly 2A), catalytic subunit, alpha isoform;
  • Gene: [05q/PROP1] prophet of Pit1, paired-like homeodomain transcription factor; pituitary hormone deficiency, combined familial (CPHD); [CPHD ]
  • Gene: [05q/RGS14] regulator of G-protein signalling 14;
  • Gene: [05q/RPS20A] ribosomal protein S20a (gene or pseudogene);
  • Gene: [05q/UBE2B] ubiquitin-conjugating enzyme E2B (RAD6B homolog; 17kD);
  • Gene: [05q1/ASSP10] argininosuccinate synthetase pseudogene 10;
  • Gene: [05q1/ASSP9] argininosuccinate synthetase pseudogene 9;
  • Gene: [05q1/CCNB1] cyclin B1 (G2/mitotic specific); [CCNB ]
  • Gene: [05q1/CCNH] cyclin H (37kD);
  • Gene: [05q1/CRTLN] cartilage linking protein 1 (proteoglycan link protein); [CRTL1 ]
  • Gene: [05q1/CSPG2] chondroitin sulfate proteoglycan 2 (versican);
  • Gene: [05q1/CTLA3] cytotoxic T-lymphocyte-associated serine esterase 3; granzyme A (Hanukah factor serine protease); T cell/natural killer cells serine esterase 3;
  • Gene: [05q1/DHFR] dihydrofolate reductase; megaloblastic anemia (dihydrofolate reductase deficiency);
  • Gene: [05q1/EEF1B3] eukaryotic translation elongation factor 1 beta 3;
  • Gene: [05q1/ERVR] Wagner syndrome; erosive vitreoretinopathy; [WGN1 ]
  • Gene: [05q1/FKHL8] forkhead (Drosophila)-like 8;
  • Gene: [05q1/GTF2H2] general transcription factor IIH, polypeptide 2 (44kD subunit); [BTF2 TFIIH ]
  • Gene: [05q1/HMGCR] 3-hydroxy-3-methylglutaryl-Coenzyme A reductase;
  • Gene: [05q1/KIF2] kinesin heavy chain member 2; [HK2 ]
  • Gene: [05q1/MSH3] mutS (E. coli) homolog 3; mismatch repair protein 1; endometrial cancer; [MRP1 ]
  • Gene: [05q1/NRPB] nuclear restricted protein, BTB domain-like (brain); [PIG10 ]
  • Gene: [05q1/PMCHL2] pro-melanin-concentrating hormone-like 2;
  • Gene: [05q1/RPS23] ribosomal protein S23;
  • Gene: [05q1/THBS4] thrombospondin 4; [TSP4 ]
  • Gene: [05q1/ZNF5] zinc finger protein 5 (probe 5CMP1); [TZF2 ]
  • Gene: [05q11/HTR1A] 5-hydroxytryptamine (serotonin) receptor 1A; [ADRBRL1 ]
  • Gene: [05q11/IL6ST] interleukin 6 signal transducer, gp130 (oncostatin M receptor; antigen CDW130);
  • Gene: [05q11/LARS] leucyl-tRNA synthetase;
  • Gene: [05q112/HSPBL4] heat shock 27kD protein-like 4; [HSPL27 ]
  • Gene: [05q12/LY64] lymphocyte antigen 64 (mouse) homolog, radioprotective, 105kD; [RP105 ]
  • Gene: [05q12/PDE4D] phosphodiesterase 4D, cAMP-specific; dunce (Drosophila)-homolog phosphodiesterase E3;
  • Gene: [05q13/CDH12P] cadherin 12 (N-cadherin 2) pseudogene;
  • Gene: [05q13/F2RL1] coagulation factor II (thrombin) receptor-like 1; proteinase activated (protease-activated) receptor 2; G protein-coupled receptor 11; [PAR2 GPR11 ]
  • Gene: [05q13/F2R] coagulation factor II (thrombin) receptor; proteinase activated (protease-activated) receptor 1; [TR CF2R PAR1 ]
  • Gene: [05q13/HEXB] hexosaminidase B, beta polypeptide; gangliosidosis GM2, type II (Sandhoff disease); motor neuron disease, progressive;
  • Gene: [05q13/MAP1B] microtubule-associated protein 1B; [MAP5 ]
  • Gene: [05q13/PIK3R1] phosphatidylinositol 3-kinase, regulatory, polypeptide 1 (p85 alpha); [p85a ]
  • Gene: [05q13/RASA1] RAS p21 protein activator 1; GTPase activating protein of RAS (GAP); [GAP ]
  • Gene: [05q13/RASGRF2] Ras protein-specific guanine nucleotide-releasing factor 2;
  • Gene: [05q13/SMN1] survival of motor neuron 1, telomeric; spinal muscular atrophy, type I (infantile acute form; Werdnig-Hoffmann disease; MIM:253300); spinal muscular atrophy, type II (intermediate form; MIM:253550); spinal muscular atroph
  • Gene: [05q13/SMN2] survival of motor neuron 2, centromeric; spinal muscular atrophy, type I (infantile acute form; Werdnig-Hoffmann disease; MIM:253300);
  • Gene: [05q131/NAIP] neuronal apoptosis inhibitory protein;
  • Gene: [05q131/OCLN] occludin;
  • Gene: [05q133/ARSB] arylsulfatase B (N-acetylgalactosamine 4-sulfatase); mucopolysaccharidosis VI (Maroteaux-Lamy syndrome);
  • Gene: [05q133/CKMT2] creatine kinase, mitochondrial 2 (sarcomeric);
  • Gene: [05q14/GLRX] glutaredoxin (thioltransferase);
  • Gene: [05q14/MEF2C] MADS box transcription enhancer factor 2, polypeptide C; myocyte-specific enhancer factor 2C;
  • Gene: [05q14/TFCOUP1] transcription factor COUP 1 (chicken ovalbumin upstream promoter 1); thyroid hormone receptor-like 3 (COUP transcription factor); avian leukemia viral homolog-like 3; [ERBAL3 EAR3 ]
  • Gene: [05q15/FRA5B] fragile site 5q15, BrdU type, common;
  • Gene: [05q15/FRA5D] fragile site 5q15, aphidicolin type, common;
  • Gene: [05q2/APC] adenomatous polyposis of the colon; [FAP FPC ]
  • Gene: [05q2/CAMK4] calcium/calmodulin-dependent protein kinase (CaM kinase) 4, catalytic; calspermin;
  • Gene: [05q2/DP1] deleted in polyposis 1; [D5S346 ]
  • Gene: [05q2/HSD17B4] hydroxysteroid (17-beta) dehydrogenase 4; estradiol 17 beta-dehydrogenase 4; D-bifunctional protein deficiency;
  • Gene: [05q2/MANA2] mannosidase, alpha type II;
  • Gene: [05q2/MCC] tumor suppressor MCC (mutated in colorectal cancers); mutated in colorectal cancers; [D5S141 ]
  • Gene: [05q2/SRP19] signal recognition particle 19kD;
  • Gene: [05q21/FER] fps/fes-related tyrosine kinase (phosphoprotein NCP94);
  • Gene: [05q21/FRA5F] fragile site 5q21, aphidicolin type, common;
  • Gene: [05q21/GJA1P1] gap junction protein, alpha 1, 43kD pseudogene 1; connexin 43, pseudogene 1; [GJA1P ]
  • Gene: [05q22/CTNNAP1] catenin (cadherin-associated protein), alpha pseudogene 1;
  • Gene: [05q22/U2AF1RS1] U2 small nuclear RNP auxiliary factor 1, 35kD subunit, related subunit 1; [U2AFBPL ]
  • Gene: [05q23/CAMLG] calcium-modulating cyclophilin ligand;
  • Gene: [05q23/DHFRL2] dihydrofolate reductase like 2;
  • Gene: [05q23/DTR] diphtheria toxin receptor; heparin-binding epidermal growth factor-like growth factor; diphtheria toxin sensitivity; [DTS HEGFL ]
  • Gene: [05q233/SLC12A2] solute carrier family 12 (sodium/potassium/chloride transporters), member 2;
  • Gene: [05q3/ADRB2] adrenergic, beta-2-, receptor (surface); [ADRBR ADRB2R ]
  • Gene: [05q3/ANX6] annexin VI (calcium-binding protein p68); annexin VI (lipocortin VI; calcium-binding protein p68; calphobindin II); [CBP68 p68 p70 ]
  • Gene: [05q3/ATOX1] antioxidant protein 1 (yeast) homolog 1; [ATX1 HAH1 ]
  • Gene: [05q3/CCNG1] cyclin G1;
  • Gene: [05q3/CDX1] caudal type homeo box transcription factor 1;
  • Gene: [05q3/CSX] cardiac-specific homeo box;
  • Gene: [05q3/DTD] diastrophic dysplasia sulfate transporter; diastrophic dysplasia; atelosteogenesis type IB (MIM:600972); atelosteogenesis type II (neonatal osseous dysplasia I; MIM:256050); achondrogenesis, type IB (ACG-IB; ACG1B); [DTDST
  • Gene: [05q3/F12] coagulation factor XII (Hageman factor); Hageman clotting factor deficiency;
  • Gene: [05q3/FGF1] fibroblast growth factor 1 (acidic); endothelial cell growth factor (beta and alpha); [FGFA ECGFA ]
  • Gene: [05q3/FGFR4] fibroblast growth factor receptor 4; protein tyrosine kinase FGFR-like 4;
  • Gene: [05q3/FLT4] fms-related tyrosine kinase 4; oncogene FLT4 (src/ros/fms-related tyrosine kinase);
  • Gene: [05q3/GABRA1] gamma-aminobutyric acid (GABA) A receptor, alpha 1;
  • Gene: [05q3/GABRA6] gamma-aminobutyric acid (GABA) A receptor, alpha 6;
  • Gene: [05q3/GABRG2] gamma-aminobutyric acid (GABA) A receptor, gamma 2;
  • Gene: [05q3/GAPDL16] glyceraldehyde-3-phosphate dehydrogenase-like 16;
  • Gene: [05q3/GM2A] ganglioside GM2 activator protein; sphingolipid activator protein 3; GM2-gangliosidosis; Tay-Sachs disease, type AB; [SAP3 ]
  • Gene: [05q3/GPX3] glutathione peroxidase 3 (plasma);
  • Gene: [05q3/GRL] glucocorticoid receptor; cortisol resistance from glucocorticoid receptor defect; [GCCR GCR ]
  • Gene: [05q3/HEMANGC] hemangioma, capillary, hereditary;
  • Gene: [05q3/HMMR] hyaluronan-mediated motility receptor; [RHAMM ]
  • Gene: [05q3/HTR4] 5-hydroxytryptamine (serotonin) receptor 4; cardiac 5-HT4 (serotonin 5-HT-4A) receptor;
  • Gene: [05q3/IL12B] interleukin 12, beta (cytotoxic lymphocyte maturation factor 2, p40); natural killer cell stimulatory factor 2 (interleukin 12, beta); [NKSF2 ]
  • Gene: [05q3/ITK] protein tyrosine kinase ITK, non-receptor (T-cell-specific); T-cell-specific tyrosine kinase; homolog of mouse itk/tsk;
  • Gene: [05q3/LCP2] lymphocyte cytosolic protein 2 (SH2 domain-containing leukocyte protein of 76kD); [SLP-76 ]
  • Gene: [05q3/LECT2] leukocyte cell-derived chemotaxin 2;
  • Gene: [05q3/MFAP3] microfibrillar-associated protein 3;
  • Gene: [05q3/MSX2] msh (Drosophila) homeo box homolog 2 (homeo box 8); craniosynostosis, Boston type; [HOX8 CRS2 CSB ]
  • Gene: [05q3/NDST1] N-deacetylase/N-sulfotransferase 1 (heparan glucosaminyl); heparan sulfate-N-deacetylase/N-sulfotransferase;
  • Gene: [05q3/PDE6A] phosphodiesterase 6A, cGMP-specific, rod, alpha; retinal rod photoreceptor cGMP phosphodiesterase, alpha subunit; retinitis pigmentosa (cGMP phosphodiesterase 6A deficiency);
  • Gene: [05q3/PDGFRB] platelet-derived growth factor receptor, beta polypeptide; [PDGFR ]
  • Gene: [05q3/RPS14] ribosomal protein S14; emetine resistance; [EMTB ]
  • Gene: [05q3/RPS17L1] ribosomal protein S17a-like 1 (gene or pseudogene); [RPS17A ]
  • Gene: [05q3/RPS20B] ribosomal protein S20b (gene or pseudogene);
  • Gene: [05q3/SLC2A3P] solute carrier family 2 (facilitated glucose transporter), member 3 pseudogene; glucose transporter 3 pseudogene 1; [GLUT6 GLUT3P1 ]
  • Gene: [05q3/SM1] Schistosoma mansoni susceptibility/resistance;
  • Gene: [05q3/SPARC] secreted protein, acidic, cysteine-rich (BM-40; osteonectin); [BM-40 ]
  • Gene: [05q3/TCOF1] treacle protein; Treacher Collins-Franceschetti syndrome 1 (mandibulofacial dysostosis); [TCS MFD1 ]
  • Gene: [05q3/TTC1] tetratricopeptide repeat domain 1; [TPR1 ]
  • Gene: [05q31/CDC25C] cell division cycle 25C; protein tyrosine phosphatase CDC25C;
  • Gene: [05q31/CSF2] colony stimulating factor 2 (granulocyte-macrophage); [GMCSF ]
  • Gene: [05q31/CTNNA1] catenin (cadherin-associated protein), alpha 1 (102kD); [CAP102 ]
  • Gene: [05q31/DIAPH1] diaphanous, Drosophila, homolog of, 1; deafness, autosomal dominant 1 (Konigsmark syndrome; MIM:124900); deafness, progressive low-tone (nonsyndromic sensorineural, 1; MIM:124900); [DFNA1 LFHL1 ]
  • Gene: [05q31/HSPA4] heat shock 70kD protein 4;
  • Gene: [05q31/IL13] interleukin 13; [P600 ]
  • Gene: [05q31/IL3] interleukin 3 (colony-stimulating factor, multiple); differentiation factor for basophils (interleukin 3); [MCSF CSFM ]
  • Gene: [05q31/IL4] interleukin 4 (B cell stimulatory factor-1); [BCGF1 BSF1 ]
  • Gene: [05q31/IL5] interleukin 5 (colony-stimulating factor, eosinophil); eosinophil differentiation factor (T-cell replacing factor); [CSFE EDF TRF ]
  • Gene: [05q31/IL9] interleukin 9 (T cell-derived growth factor P40/TCGFIII); [P40 TCGFIII ]
  • Gene: [05q31/LGMD1A] limb girdle muscular dystrophy 1A (autosomal dominant; proximal); [LGMD1 ]
  • Gene: [05q31/MADH5] MAD (mothers against decapentaplegic, Drosophila) homolog 5; [SMAD5 JV5-1 ]
  • Gene: [05q31/MGAT1] mannosyl (alpha-1,3-)-glycoprotein beta-1,2-N-acetylglucosaminyltransferase;
  • Gene: [05q31/NDUFA2] NADH dehydrogenase (ubiquinone) 1 alpha subcomplex, 2 (8kD, B8);
  • Gene: [05q31/NPY6R] neuropeptide Y receptor Y6; neuropeptide Y receptor Y1-like; pancreatic polypeptide receptor 2; [PP2 ]
  • Gene: [05q31/PITX1] pituitary homeo box 1; paired-like homeodomain transcription factor 1; backfoot (mouse) homolog; [PTX1 BFT ]
  • Gene: [05q31/POU4F3] POU domain, class 4, transcription factor 3; deafness, autosomal dominant 15 (MIM:602459); [BRN3C DFNA15 ]
  • Gene: [05q31/RAD50] RAD50 (S. cerevisiae) homolog;
  • Gene: [05q31/SEPP1] selenoprotein P, plasma, 1;
  • Gene: [05q31/SLC22A5] solute carrier family 22 (organic cation transporter), member 5; carnitine transporter, membrane; carnitine deficiency, systemic primary (MIM:212140); [OCTN2 CDSP ]
  • Gene: [05q31/TCEB1L] transcription elongation factor B (SIII), polypeptide 1-like; organ of Corti protein 2; [OCP2 ]
  • Gene: [05q31/TGFBI] transforming growth factor, beta-induced, 68kD (keratoepithelin); corneal stromal dystrophy 1 (lattice corneal dystrophy type 1; MIM:122200); corneal stromal dystrophy 2 (granular type; Reis-Bucklers type; Groenouw type
  • Gene: [05q311/FRA5C] fragile site 5q31.1, aphidicolin type, common;
  • Gene: [05q311/HSPA9] heat shock 70kD protein 9 (mortalin); glucose regulated protein (75kD); mortalin-2, cytosolic, (mouse) homolog; mitochondrial stress-70 protein; peptide-binding protein 74; [GRP75 MOT-2 ]
  • Gene: [05q311/IGES] immunoglobulin E concentration, serum;
  • Gene: [05q311/IRF1] interferon regulatory factor 1 (activator);
  • Gene: [05q311/TCF7] transcription factor 7 (T-cell specific, HMG-box); [TCF-1 ]
  • Gene: [05q312/HINT] histidine triad nucleotide-binding protein; protein kinase C inhibitor 1; protein kinase C interacting protein 1; [PRKCNH1 PKCI1 ]
  • Gene: [05q32/GLRA1] glycine receptor, alpha 1; startle disease/hyperekplexia (stiff man syndrome; Kok disease; MIM:149400); [STHE ]
  • Gene: [05q32/HLADG] HLA-D, class II, gamma polypeptide (p33; invariant; antigen CD74); CD74 antigen (p33; invariant polypeptide of MHC class II antigen-associated); [DHLAG CD74 ]
  • Gene: [05q32/PCDH1] protocadherin 1 (cadherin-like 1); [pc42 ]
  • Gene: [05q32/PCDH2] protocadherin 2 (cadherin-like 2); [pc43 ]
  • Gene: [05q33/ADRA1B] adrenergic, alpha-1B-, receptor; [ADRA1 ]
  • Gene: [05q33/CSF1R] colony stimulating factor 1 (macrophage-specific, CSF-M) receptor; McDonough feline sarcoma viral homolog; friend-murine leukemia virus integration site 2 homolog; anemia macrocytic, refractory (5q-minus syndrome
  • Gene: [05q33/GLULL1] glutamate-ammonia ligase (glutamine synthase)-like 1;
  • Gene: [05q33/GRIA1] glutamate receptor, ionotropic, AMPA 1; [GLUR1 ]
  • Gene: [05q33/SGCD] sarcoglycan, delta (dystrophin associated glycoprotein, 35kD); limb-girdle muscular dystrophy 2F (MIM:601287); [SGD DAGD ]
  • Gene: [05q333/RPL7P] ribosomal protein L7 pseudogene; [RPL17P ]
  • Gene: [05q34/DUSP1] dual specificity phosphatase 1 (EC:3.1.3.48 and EC:3.1.3.16); protein-tyrosine phosphatase, nonreceptor type, 10; MAP kinase phosphatase 1;
  • Gene: [05q34/EBF] early B-cell factor; olfactory neuronal transcription factor OLF1; [OLF1 ]
  • Gene: [05q34/FKHL10] forkhead (Drosophila)-like 10;
  • Gene: [05q34/GABRB2] gamma-aminobutyric acid (GABA) A receptor, beta 2;
  • Gene: [05q34/KCNMB1] potassium large conductance calcium-activated channel, subfamily M, beta member 1; slowpoke (Drosophila) homolog, beta; [SLOB ]
  • Gene: [05q35/AMCN] arthrogryposis multiplex congenita, neurogenic; [AMC ]
  • Gene: [05q35/CANX] calnexin (MHC class I antigen-binding);
  • Gene: [05q35/CHR] chromate resistance (sulfate transport?);
  • Gene: [05q35/FKHRP1] forkhead (Drosophila) homolog (rhabdomyosarcoma) pseudogene 1;
  • Gene: [05q35/FRA5G] fragile site, folic acid type, rare, fra(5)(q35);
  • Gene: [05q35/GPRK6] G protein-coupled receptor kinase 6;
  • Gene: [05q35/GRM6] glutamate receptor, metabotropic 6;
  • Gene: [05q35/LTC4S] leukotriene C4 synthase;
  • Gene: [05q35/NPM1] nucleophosmin (nucleolar phosphoprotein B23, numatrin); non-Hodgkin's lymphoma with t(2;5)(p23;q35); myelodysplastic syndrome and acute myeloid leukemia with t(3;5)(q25.1;q35);
  • Gene: [05q35/PIGFP1] phosphatidylinositol glycan, class F, pseudogene 1;
  • Gene: [05q35/PRKM9] protein kinase, mitogen-activated 9 (MAP kinase); stress-activated protein kinase 2; c-jun N-terminal kinase 2;
  • Gene: [05q35/SLC17A2] solute carrier family 17 (sodium phosphate), member 2; [NPT2 NAPI-3 ]
  • Gene: [05q35/SNCB] synuclein, beta;
  • Gene: [05q351/DRD1] dopamine receptor D1; [DRD1A ]
  • Gene: [05q352/HK3] hexokinase 3;
  • Gene: [05q353/HNRPH1] heterogeneous nuclear ribonucleoprotein H1 (H); RNP particle, heterogeneous nuclear, H1 protein; [D8P49 ]
  • Gene: [05q353/TCF17] transcription factor 17; [KID-1 ]
  • Gene: [05^/ACTBP2] actin, beta pseudogene 2;
  • Gene: [05^/ACTBP4] actin, beta pseudogene 4;
  • Gene: [05^/CART] cocaine- and amphetamine-regulated transcript;
  • Gene: [05^/CKN1] Cockayne syndrome A protein (WD-repeat protein); Cockayne syndrome 1 (classical form A); [CSA ]
  • Gene: [05^/DBN1] drebrin 1;
  • Gene: [05^/ERVPL2] endogenous retroviral sequence pol-like 2; [ERPL2 ]
  • Gene: [05^/FTHL10] ferritin, heavy polypeptide-like 10;
  • Gene: [05^/GABRIL1] diazepam binding inhibitor, like 1; [DBIL1 ]
  • Gene: [05^/GP36B] glycoprotein GP36b (of the endoplasmic reticulum);
  • Gene: [05^/HARSR] histidyl-tRNA synthetase related gene;
  • Gene: [05^/HARS] histidyl-tRNA synthetase;
  • Gene: [05^/ITGA1] integrin, alpha 1 (antigen CD49A); [CD49A Vla-1 ]
  • Gene: [05^/MEKK1] MAP/ERK kinase kinase 1; MAP kinase kinase kinase 1; MEK kinase;
  • Gene: [05^/MSK11] antigen MSK11 (monoclonal antibody SR84);
  • Gene: [05^/PCH2] protein spot in 2-D gels (MM 250 kD; pI 8.3);
  • Gene: [05^/RAB9P] oncogene RAS-family, member rab9 pseudogene;
  • Gene: [05^/RARS] arginyl-tRNA synthetase;
  • Gene: [05^/RPL37] ribosomal protein L37;
  • Gene: [05^/SLC22A4] solute carrier family 22 (organic cation transporter), member 4; [OCTN1 ]
  • Gene: [05^/SPINK1] serine protease inhibitor, Kazal type 1; pancreatic secretory trypsin inhibitor; [PSTI ]
  • Gene: [05^/SUP45L1] sup45 (yeast omnipotent suppressor 45) homolog-like 1;
  • Gene: [05^/TCP1L2] t-complex 1-like 2;
  • Gene: [05^/TRP3] tRNA proline (anticodon UGG) 3;
  • Gene: [05^/TRT1] tRNA threonine (anticodon UGU) 1;
  • Gene: [05^/TRV1] tRNA valine 1; [TRV ]
  • Gene: [05^/UNG2] uracil-DNA glycosylase 2;
  • Gene: [05^/UQCRBP] ubiquinol-cytochrome c reductase binding protein-like;
  • Gene: [05^/XBPP1] X-box binding protein pseudogene 1; [XBP1 ]
  • Gene: [05^/XRCC4] X-ray repair complementing defective repair in Chinese hamster cells 4;
  • Gene: [05^/ZNF3] zinc finger protein 3 (A8-51);
  • Gene: [06p/CBFA1] core-binding factor, runt domain, alpha subunit 1; cleidocranial dysplasia 1 (MIM:119600); [AML3 PEBP2A1 ]
  • Gene: [06p/CSCI] corticosterone side-chain isomerase;
  • Gene: [06p/CSNK2B] casein kinase 2, beta polypeptide (phosvitin);
  • Gene: [06p/FTHP1] ferritin, heavy polypeptide pseudogene 1; [FTHL5 ]
  • Gene: [06p/MCM3] minichromosome maintenance deficient (S.cerevisiae) 3; DNA replication licensing factor MCM3; DNA polymerase alpha holoenzyme-associated protein P1;
  • Gene: [06p/PAFAH] platelet-activating factor acetylhydrolase (plasma); platelet-activating factor acetylhydrolase deficiency;
  • Gene: [06p/PGK1P2] phosphoglycerate kinase 1 pseudogene 2;
  • Gene: [06p/PKHD1] polycystic kidney and hepatic disease 1 (autosomal recessive); [ARPKD ]
  • Gene: [06p/PTK7] protein tyrosine kinase PTK7; colon carcinoma kinase 4;
  • Gene: [06p/RDS] peripherin (retinal degeneration slow protein); retinal degeneration, slow; retinitis pigmentosa 7 (autosomal dominant); [RP7 ]
  • Gene: [06p/RHAG] Rhesus blood group-associated glycoprotein, 50kD; Rh deficiency syndrome (RH-null hemolytic anemia; MIM:268150); [RH50A ]
  • Gene: [06p1/BPAG1] bullous pemphigoid antigen 1 (230/240kD); epidermolysis bullosa, generalized atrophic benign (MIM:226650); [BP240 ]
  • Gene: [06p1/EJM1] epilepsy, juvenile myoclonic 1 (Janz syndrome); [EJM ]
  • Gene: [06p1/FTHL15] ferritin, heavy polypeptide-like 15;
  • Gene: [06p1/KRAS1P] Kirsten rat sarcoma 1 viral homolog, pseudogene; [RASK1 ]
  • Gene: [06p1/PRIM2A] primase polypeptide 2A (58kD);
  • Gene: [06p1/PRIM2B] primase polypeptide 2B (58kD);
  • Gene: [06p12/CACTP] carnitine-acylcarnitine translocase pseudogene;
  • Gene: [06p12/GLCLC] glutamate-cysteine ligase (gamma-glutamylcysteine synthetase), catalytic (72.8kD); hereditary hemolytic anemia (due to gamma-glutamylcysteine synthetase deficiency);
  • Gene: [06p12/GSTAP1] glutathione S-transferase A pseudogene 1;
  • Gene: [06p12/GSTAP2] glutathione S-transferase A pseudogene 2;
  • Gene: [06p12/HNRPG] heterogeneous nuclear ribonucleoprotein G; RNP particle, heterogeneous nuclear, G protein;
  • Gene: [06p12/HSPCB] heat shock 90kD protein 1, beta; [HSP90B HSP84 ]
  • Gene: [06p12/NYS2] nystagmus 2, congenital autosomal dominant; [NYSA ]
  • Gene: [06p12/TFAP2B] transcription factor AP-2 beta (activating enhancer-binding protein 2 beta);
  • Gene: [06p12/VEGF] vascular endothelial growth factor;
  • Gene: [06p122/GSTA1] glutathione S-transferase A1 (alpha class; H-a1; liver); hyperbilirubinemia, non-hemolytic unconjugated (in the newborn);
  • Gene: [06p122/GSTA2] glutathione S-transferase A2 (alpha class; H-a2; liver);
  • Gene: [06p2/BCKDE1B] 2-oxoisovalerate dehydrogenase (lipoamide), beta polypeptide; branched chain keto acid dehydrogenase E1, beta polypeptide; maple syrup urine disease (due to BCK-E1-beta deficiency);
  • Gene: [06p2/BTN] butyrophilin;
  • Gene: [06p2/CLPS] colipase, pancreatic (12kD);
  • Gene: [06p2/DSP] desmoplakin (DPI, DPII);
  • Gene: [06p2/ELANH2] protease inhibitor 2 (anti-elastase), monocyte/neutrophil derived; [PI2 ]
  • Gene: [06p2/F13A1] coagulation factor XIII, A1 polypeptide; fibrin stabilizing factor, A1 subunit; glutaminyl-peptide gamma-glutamyltransferase, A1 subunit; transglutaminase, plasma (fibrinoligase), A1 subunit;
  • Gene: [06p2/FIM1] friend-murine leukemia virus integration site 1 homolog;
  • Gene: [06p2/H1F3] H1 histone family, member 3;
  • Gene: [06p2/H1F5] H1 histone family, member 5; [H1.5 ]
  • Gene: [06p2/H2AFA] H2A histone family, member A; [H2A/a ]
  • Gene: [06p2/H2AFC] H2A histone family, member C; [H2A/c ]
  • Gene: [06p2/H2AFD] H2A histone family, member D; [H2A/d ]
  • Gene: [06p2/H2AFE] H2A histone family, member E; [H2A/e ]
  • Gene: [06p2/H2AFG] H2A histone family, member G; [H2A/g ]
  • Gene: [06p2/H2AFI] H2A histone family, member I; [H2A/i ]
  • Gene: [06p2/H2AFN] H2A histone family, member N; [H2A/n H2A.1 ]
  • Gene: [06p2/H2BFC] H2B histone family, member C; [H2B/c ]
  • Gene: [06p2/H2BFD] H2B histone family, member D; [H2B/d ]
  • Gene: [06p2/H2BFE] H2B histone family, member D; [H2B/d ]
  • Gene: [06p2/H2BFN] H2B histone family, member N; [H2B/n H2B.2 ]
  • Gene: [06p2/H3FF] H3 histone family, member F; [H3/f ]
  • Gene: [06p2/H3FJ] H3 histone family, member J; [H3/j ]
  • Gene: [06p2/H3FK] H3 histone family, member K; [H3/k ]
  • Gene: [06p2/H4FD] H4 histone family, member D; [H4/d ]
  • Gene: [06p2/H4FE] H4 histone family, member E; [H4/e ]
  • Gene: [06p2/H4FK] H4 histone family, member K; [H4/k ]

    •