Gene: [17q2/DDX5] DEAD/H (Asp-Glu-Ala-Asp/His) box polypeptide 5 (RNA helicase, 68kD); RNA-dependent ATPase 1 (nuclear; p68; RNA-helicase 1); — Gene: [19q13/FPRL2] formyl peptide receptor-like 2;

Gene: [17q2/KRT10] keratin 10, type I, alpha, acidic (pI 5.3; 56.5kD); epidermolytic hyperkeratosis (keratosis palmaris et plantaris; MIM:113800); [CYKA10 ]

Gene: [17q2/KRT13] keratin 13, type I, alpha, acidic (pI 5.1; 54kD); white sponge nevus (MIM:193900); [CYKA13 KRTB ]

Gene: [17q2/KRT14] keratin 14, type I, alpha, acidic (pI 5.3; 50kD); epidermolysis bullosa simplex (Dowling-Meara type; MIM:131760); epidermolysis bullosa simplex (Weber-Cockayne type; MIM:131800); epidermolysis bullosa simplex (EBS2; gener

Gene: [17q2/KRT15] keratin 15, type I, alpha, acidic (pI 4.9; 50kD); [CYKA15 CYK13 ]

Gene: [17q2/KRT16] keratin 16, type I, alpha, acidic (pI 5.1; 48kD); pachyonychia congenita (Jadassohn-Lewandowsky type; MIM:167200); nonepidermolytic palmoplantar keratoderma; [CYKA16 ]

Gene: [17q2/KRT17] keratin 17, type I, alpha, acidic (pI 5.1; 46kD); pachyonychia congenita 1 (Jackson-Lawler type; MIM:167210); [CYKA17 PC ]

Gene: [17q2/KRT19] keratin 19, type I, alpha, acidic (pI 5.2; 40kD); [CYKA19 ]

Gene: [17q2/MIC6] antigen MIC6 (monoclonal antibody H207); [H207 ]

Gene: [17q2/MKS] dysencephalia splanchnocystica (Meckel-Gruber syndrome);

Gene: [17q2/MPO] myeloperoxidase; myeloperoxidase deficiency;

Gene: [17q2/MSK18] antigen MSK18 (monoclonal antibody J143);

Gene: [17q2/MYL4] myosin, light polypeptide 4, alkali; atrial, embryonic; [MYLF ]

Gene: [17q2/NGFR] nerve growth factor receptor;

Gene: [17q2/NSF] N-ethylmaleimide-sensitive factor (vesicular-fusion protein NSF);

Gene: [17q2/PEPE] peptidase E;

Gene: [17q2/PNMT] phenylethanolamine N-methyltransferase;

Gene: [17q2/PRKAR1A] protein kinase, cAMP-dependent, regulatory subunit, type I, alpha; tissue-specific extinguisher 1;

Gene: [17q2/PRKCA] protein kinase C, alpha polypeptide;

Gene: [17q2/PSORS2] psoriasis susceptibility locus 2 (psoriasin?); [PSOR ]

Gene: [17q2/RAC3] ras-related C3 botulinum toxin substrate 3; rho family, small GTP binding protein Rac3;

Gene: [17q2/RAD51C] RAD51 (S. cerevisiae) homolog C; [RAD51L2 ]

Gene: [17q2/RP17] retinitis pigmentosa 17 (autosomal dominant);

Gene: [17q2/RPL27] ribosomal protein L27;

Gene: [17q2/RPL38] ribosomal protein L38;

Gene: [17q2/SCN4A] sodium channel, voltage-gated, type IV, alpha polypeptide (adult muscle); hyperkalemic periodic paralysis (HYPP; Gamstorp disease; myotonia; adynamia episodica hereditaria); paramyotonia congenita (of von Eulenburg; MIM:1

Gene: [17q2/SFRS1] splicing factor, arginine/serine-rich 1 (alternate splicing factor/splicing factor 2); [ASF SF2 ]

Gene: [17q2/SHCL1] SHC (Src homology 2 domain-containing) transforming protein-like 1;

Gene: [17q2/SOX9] SRY (sex-determining region Y)-box 9; campomelic dysplasia, autosomal sex-reversal (campomelic dwarfism); [SRA1 CMD1 ]

Gene: [17q2/SUPT4H1] suppressor of Ty (S.cerevisiae) 4 homolog 1; [SPT4H ]

Gene: [17q2/SYM1] symphalangism 1 (proximal; hereditary absence of the proximal interphalangeal joints);

Gene: [17q2/TBX4] T-box 4;

Gene: [17q2/TK1] thymidine kinase, soluble;

Gene: [17q2/TNFAI1] tumor necrosis factor, alpha-induced protein 1 (endothelial); [TNFAIP1 EDP1 ]

Gene: [17q2/TOP2A] topoisomerase (DNA) II alpha (170kD);

Gene: [17q2/UMPH2] uridine 5'-monophosphate phosphohydrolase 2; 5'-nucleotidase 2 (pyrimidine specific);

Gene: [17q2/ZNF147] zinc finger protein 147 (estrogen-responsive finger protein);

Gene: [17q21/ACACA] acetyl-CoA carboxylase alpha (265kD; EC:6.4.1.2); biotin carboxylase (EC:6.3.4.14); acetyl-CoA carboxylase deficiency;

Gene: [17q21/AOC2] amine oxidase, copper containing 2 (retina-specific);

Gene: [17q21/ATP6N1] ATPase, H+ transporting, lysosomal (vacuolar proton pump) non-catalytic accessory protein 1 (116kD); vacuolar proton pump 1 (116kD);

Gene: [17q21/BRCA1] oncogene BRCA1; breast cancer 1, early onset;

Gene: [17q21/CNP] 2',3'-cyclic nucleotide 3'phosphohydrolase;

Gene: [17q21/DUSP3] dual specificity phosphatase 3 (EC:3.1.3.48 and EC:3.1.3.16); vaccinia virus phosphatase VH1-related;

Gene: [17q21/ETV4] ets translocation variant gene 4 (adenovirus E1A enhancer-binding protein, E1AF); [E1A-F ]

Gene: [17q21/EZH1] enhancer of zeste (Drosophila) homolog 1;

Gene: [17q21/FGF11] fibroblast growth factor 11; [FHF3 ]

Gene: [17q21/G6PC] glucose-6-phosphate, catalytic; glycogen storage disease type Ia (von Gierke disease);

Gene: [17q21/GCN5L2] GCN5 (general control of amino-acid synthesis, yeast, homolog)-like 2;

Gene: [17q21/GFA] glial fibrillary acidic protein; [GFAP ]

Gene: [17q21/GNGT2] guanine nucleotide binding protein (G protein), gamma transducing activity polypeptide 2; adenylate cyclase transductor GT, gamma-T2; [GNGT8 ]

Gene: [17q21/GPR2] G protein-coupled receptor 2;

Gene: [17q21/HCRT] hypocretin (orexin) neuropeptide precursor; [PPOX ]

Gene: [17q21/IFNI35] interferon-induced protein 35; [IFI35 ]

Gene: [17q21/JUP] junction plakoglobin (desmoplakin III); [DP3 DP DSP ]

Gene: [17q21/KRT9] keratin 9, type I, alpha, acidic (pI 5.4; 64kD); epidermolytic palmoplantar keratoderma; [CYKA9 ]

Gene: [17q21/MAPT] microtubule-associated protein tau; Alzheimer disease susceptibility locus x?; frontotemporal dementia, with parkinsonism; [MTBT1 A68 ]

Gene: [17q21/MEOX1] mesenchyme homeo box 1; [MOX1 ]

Gene: [17q21/MLLT6] myeloid/lymphoid or mixed-lineage leukemia (trithorax (Drosophila) homolog); translocated to, 6; [AF17 ]

Gene: [17q21/NAGLU] N-acetylglucosaminidase, alpha- (Sanfilippo disease IIIB); mucopolysaccharidosis type IIIB (alpha-N-acetylglucosaminidase deficiency); SanFilippo syndrome B (alpha-N-acetylglucosaminidase deficiency);

Gene: [17q21/PHB] prohibitin;

Gene: [17q21/PTP4AP1] protein tyrosine phosphatase 4A pseudogene 1; [HH18 ]

Gene: [17q21/RHO7] GTP-binding protein Rho7;

Gene: [17q21/RNU2] RNA, U2 small nuclear;

Gene: [17q21/RPL34] ribosomal protein L34;

Gene: [17q21/SCYA11] small inducible cytokine subfamily A (Cys-Cys), member 11 (eotaxin);

Gene: [17q21/SGCA] sarcoglycan, alpha (dystrophin-associated glycoprotein, 50kD); adhalin (dystrophin-associated glycoprotein, 50kD); dystroglycan 2 (dystrophin-associated glycoprotein, 50kD); limb girdle muscular dystrophy 2D (autosomal re

Gene: [17q21/SLC4A1] solute carrier family 4, anion exchanger, member 1; erythrocyte membrane protein band 3; Diego blood group (MIM:110500); Waldner blood group (Wd(a) antigenic expression; MIM:112010); Wright blood group antigen (MIM:1120

Gene: [17q21/STAT3] signal transducer and activator of transcription 3, 80kD/89kD (acute-phase response factor); [APRF ]

Gene: [17q21/TADA2L] transcriptional adaptor 2 (ADA2, yeast, homolog)-like; [hADA2 ]

Gene: [17q21/UBTF] upstream binding transcription factor, RNA polymerase I;

Gene: [17q21/VAT1] synaptic vesicle membrane protein vatI homolog;

Gene: [17q21/WNT15] wingless-type MMTV integration site 15, human homolog;

Gene: [17q21/WNT3] wingless-type MMTV integration site 3; oncogene INT4/WNT3; murine mammary tumor virus oncogene homolog (WNT3); [INT4 ]

Gene: [17q211/ACLY] ATP citrate lyase (citrate cleavage enzyme);

Gene: [17q211/FZD2] frizzled (Drosophila) homolog 2;

Gene: [17q211/M17S2] membrane component, chromosome 17, surface marker 2; ovarian carcinoma antigen CA125;

Gene: [17q211/PPY] pancreatic polypeptide Y; [PNP ]

Gene: [17q211/PYY] peptide YY;

Gene: [17q211/TCFL4] transcription factor-like 4;

Gene: [17q212/CA9] membrane antigen MN; carbonic anhydrase IX;

Gene: [17q212/RABL] RAB, member of RAS oncogene family-like;

Gene: [17q213/CDC18L] cell division cycle 18-like (p62; homologous to CDC18 of S.pombe and CDC6 of S.cerevisiae); [CDC6 p62 ]

Gene: [17q213/MDC] metalloproteinase-like, disintegrin-like, cysteine-rich protein; a disintegrin and metalloprotease domain 11;

Gene: [17q213/MUL] Mulibrey nanism (Perheentupa syndrome);

Gene: [17q213/NFE2L1] transcription factor 11 (basic leucine zipper type; HBZ17; LCR-F1); nuclear factor, erythroid-derived 2-like 1; NFE2-related transcription factor 1 (NRF1); locus control region, beta (MIM:152424); [NRF1 LCRB LCR ]

Gene: [17q213/NME1] nucleoside diphosphate kinase A; metastasis inhibition factor NM23-H1; non-metastatic cells 1, protein expressed in (NM23A); neuroblastoma;

Gene: [17q213/NME2] nucleoside diphosphate kinase B; metastasis inhibition factor NM23-H2; non-metastatic cells 2, protein (NM23B) expressed in;

Gene: [17q2132/ITGA2B] integrin, alpha 2b (antigen CD41B); coagulation factor I receptor, alpha subunit; fibrinogen receptor on platelets, alpha subunit; glycoprotein IIb (platelet IIb/IIIa complex); thrombasthenia, Glanzmann-Naegeli type (

Gene: [17q2132/ITGB3] integrin, beta 3 (antigen CD61); fibrinogen receptor on platelets, beta subunit; coagulation factor I receptor, beta subunit; glycoprotein IIIa (platelet GPIIb/IIIa complex); neonatal alloimmune thrombocytopenia; [GP3A

Gene: [17q2133/CHAD] chondroadherin;

Gene: [17q2133/DLX4] distal-less homeo box 4; [DLX7 DLX8 ]

Gene: [17q22/BCL5] B-cell chronic lymphatic leukemia 5 (B-CLL: lymphoma 5); [BCL3 ]

Gene: [17q22/HLF] hepatic leukemia factor; hepatic leukemia?;

Gene: [17q23/CA4] carbonic anhydrase IV, membrane-bound;

Gene: [17q23/CD79B] antigen CD79 beta; immunoglobulin-associated beta (B29); [IGB B29 ]

Gene: [17q23/DCP1] dipeptidyl carboxypeptidase 1 (angiotensin I converting enzyme); peptidyl dipeptidase A (peptidase P; angiotensin I-converting enzyme);

Gene: [17q23/GAA] glucosidase, alpha (lysosomal; acid maltase); glycogen storage disease II (glycogenosis; Pompe disease);

Gene: [17q23/KPNA2] karyopherin (importin) alpha 2 (SRP1-alpha); RAG (recombination activating gene) cohort 1; [RCH1 ]

Gene: [17q23/PECAM1] platelet/endothelial cell adhesion molecule (CD31); graft-versus-host disease (GVHD), association with; [CD31 GVHD ]

Gene: [17q23/PSMC5] proteasome (prosome, macropain) 26S subunit, ATPase, 5 (homolog of yeast Sug1); thyroid hormone receptor interactor 1; [P45 TRIP1 S8 ]

Gene: [17q23/SMARCD2] SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily d, member 2; chromatin remodeling complex, BRG1-associated factor, 60kD, B; [BAF60B ]

Gene: [17q23/TBX2] T-box 2;

Gene: [17q231/FRA17B] fragile site 17q23.1, aphidicolin type, common;

Gene: [17q24/CACNG] calcium channel, voltage-dependent, gamma subunit; calcium channel, L type, gamma polypeptide (skeletal muscle); [CACNLG ]

Gene: [17q24/CCA1] cataract, congenital, cerulean type, 1;

Gene: [17q24/FALZ] fetal Alzheimer antigen; [FAC1 ]

Gene: [17q24/SSTR2] somatostatin receptor 2;

Gene: [17q24/TOC] tylosis with oesophageal cancer; [TOCG ]

Gene: [17q25/AANAT] arylalkylamine N-acetyltransferase;

Gene: [17q25/ACOX1] acyl-CoA oxidase 1, palmitoyl, peroxisomal; pseudoneonatal adrenoleukodystrophy (peroxisomal acyl-CoA oxidase deficiency);

Gene: [17q25/ACTG1] actin, gamma 1, cytoplasmic; [ACTG ]

Gene: [17q25/CBX2] chromobox homolog 2 (Drosophila Polycomb class);

Gene: [17q25/CD7] antigen CD7 (p41; monoclonal antibodies 3A1,4A,TR41,Tp40); [p41 ]

Gene: [17q25/CDR3] cerebellar degeneration-related autoantigen 3 (52kD); paraneoplastic cerebellar degeneration-associated antigen;

Gene: [17q25/CSNK1D] casein kinase 1, delta polypeptide;

Gene: [17q25/EIF5AP2] eukaryotic translation initiation factor 5A pseudogene 2;

Gene: [17q25/EVPL] envoplakin;

Gene: [17q25/FASN] fatty acid synthase;

Gene: [17q25/GCGR] glucagon receptor; [GGR ]

Gene: [17q25/GRIN2C] glutamate receptor, ionotropic, N-methyl-D-aspartate 2C; N-methyl D-aspartate receptor channel, subunit epsilon 3; [NMDAR2C ]

Gene: [17q25/H3F3B] H3 histone, family 3B (predominant form in nondividing cells); [H3.3B ]

Gene: [17q25/ILF1] interleukin enhancer binding factor 1; [ILF ]

Gene: [17q25/LGALS3BP] lectin, galactoside-binding, soluble, 3 binding protein; galectin 3 binding protein;

Gene: [17q25/MAFG] v-maf avian musculoaponeurotic fibrosarcoma (avian) oncogene family, protein G; basic leucine zipper transcription factor MafG;

Gene: [17q25/NAPB] neuritis with brachial predilection; brachial plexus neuropathy, hereditary; amyotrophy, hereditary neuralgic, with predilection for brachial plexus; [HNA ]

Gene: [17q25/NPTX1] pentraxin I;

Gene: [17q25/P4HB] procollagen-proline, 2-oxoglutarate 4-dioxygenase (EC:1.14.11.2), beta; prolyl 4-hydroxylase (EC:1.14.11.2), beta; protein disulfide isomerase (EC:5.3.4.1); glutathione-insulin transhydrogenase (EC:1.8.4.2); thyroid hormo

Gene: [17q25/PDE6G] phosphodiesterase 6G, cGMP-specific, rod, gamma; retinal rod photoreceptor cGMP phosphodiesterase, gamma subunit;

Gene: [17q25/RPML12] ribosomal protein, mitochondrial, L12; [MRPL12 Mrp17 ]

Gene: [17q25/SEC14L] SEC14 (S. cerevisiae)-like;

Gene: [17q25/SECTM1] secreted and transmembrane 1 (protein K12); [K12 ]

Gene: [17q25/SFRS2] splicing factor, arginine/serine-rich 2 (splicing component, 35kD); [SC-35 PR264 ]

Gene: [17q25/THRBL] avian erythroblastic leukemia viral homolog 2-like; thyroid hormone receptor beta-2-like; [ERBA2L ]

Gene: [17q25/TIMP2] tissue inhibitor of metalloproteinase 2;

Gene: [17q253/ARHGDIA] GDP association inhibitor, Aplasia-ras related 1; Rho GDP dissociation inhibitor (GDI) alpha; [GDIA1 ]

Gene: [17q253/SEC7] SEC7 (S. cerevisiae)-like; [D17S811E ]

Gene: [17q253/SGSH] N-sulfoglucosamine sulfohydrolase (sulfamidase); sulphamidase, heparan sulfate sulfatase; mucopolysaccharidosis type IIIA (heparan sulfate sulfatase deficiency); SanFilippo syndrome A (heparan sulfate sulfatase deficienc

Gene: [17^/ALOX12P1] arachidonate 12-lipoxygenase pseudogene 1;

Gene: [17^/ALOX15] arachidonate 15-lipoxygenase;

Gene: [17^/ATP1B2] ATPase, Na+,K+ transporting, beta 2 polypeptide;

Gene: [17^/ATP5BL2] ATP synthase, H+ transporting, mitochondrial F1 complex, beta polypeptide-like 2; [ATPMBL2 ]

Gene: [17^/CALM2P1] calmodulin 2 (phosphorylase kinase, delta) pseudogene 1;

Gene: [17^/DVL2] dishevelled 2 (phosphoprotein; homologous to Drosophila dsh);

Gene: [17^/EFTUP] translation elongation factor Tu, mitochondrial, pseudogene; [TUFML ]

Gene: [17^/FTHL14] ferritin, heavy polypeptide-like 14;

Gene: [17^/G6PDL] glucose-6-phosphate dehydrogenase-like;

Gene: [17^/GRN] granulin;

Gene: [17^/HRP1] hyperpolymorphic gene 1; [TRE17 ]

Gene: [17^/KCNJ2] potassium inwardly-rectifying channel, subfamily J, member 2;

Gene: [17^/LIG3] ligase III, DNA, ATP-dependent;

Gene: [17^/MEIS3] homeobox protein Meis (mouse) homolog 3; [MRG2 ]

Gene: [17^/NOS2B] nitric oxide synthase 2B;

Gene: [17^/NOS2C] nitric oxide synthase 2C;

Gene: [17^/PYCR1] pyrroline-5-carboxylate reductase 1;

Gene: [17^/S9] surface antigen S9 (chromosome 17); [SA17 ]

Gene: [17^/TEX4] testis-expressed sequence 4;

Gene: [18p1/DYT7] dystonia 7, torsion (autosomal dominant);

Gene: [18p11/ADCYAP1] adenylate cyclase activating polypeptide 1 (pituitary); pituitary adenylate cyclase activating polypeptide (PACAP); [PACAP ]

Gene: [18p11/ZFP161] zinc finger protein homologous to Zfp161 in mouse;

Gene: [18p112/C18ORF1] C18orf1 (clone 22 gene);

Gene: [18p112/EIF4A2] eukaryotic translation initiation factor 4A, isoform 2;

Gene: [18p112/ERV1] endogenous retroviral sequence 1;

Gene: [18p112/GNAL] guanine nucleotide binding protein (G protein), alpha stimulating activity polypeptide, olfactory type; adenylate cyclase stimulator, olfactory type;

Gene: [18p112/MC2R] melanocortin 2 receptor (adrenocorticotropic hormone receptor); familial glucocorticoid deficiency; [ACTHR ]

Gene: [18p112/MC5R] melanocortin 5 receptor;

Gene: [18p112/PTPN2] protein tyrosine phosphatase, non-receptor type 2;

Gene: [18p112/PTPRM] protein tyrosine phosphatase, receptor type, mu polypeptide;

Gene: [18p113/HPE4] holoprosencephaly 4;

Gene: [18p113/IL9RP4] interleukin 9 receptor pseudogene 4;

Gene: [18p1131/LAMA1] laminin, alpha 1 (laminin A); [LAMA ]

Gene: [18p1131/NDUFV2] NADH dehydrogenase (ubiquinone) flavoprotein 2 (24kD; EC:1.6.5.3, EC:1.6.99.3);

Gene: [18p1132/LMCM] multiple hereditary cutaneous leiomyomata; [MCL ]

Gene: [18q/MBD1] methyl-CpG binding domain protein 1; [PCM1 MECP1 ]

Gene: [18q/PRKM4] protein kinase, mitogen-activated 4; MAP kinase 4 (p63); extracellular signal-regulated kinase 4 (p63);

Gene: [18q/SLC14A1] solute carrier family 14 (urea transporter), member 1; Kidd blood group antigen; urea transporter 1, erythrocyte; [JK UTE ]

Gene: [18q/SLC14A2] solute carrier family 14 (urea transporter), member 2; urea transporter 2, kidney; [UT2 HUT2 ]

Gene: [18q/ZNF47] zinc finger protein 47;

Gene: [18q1/AQP4] aquaporin 4;

Gene: [18q11/GATA6] GATA-binding protein 6;

Gene: [18q11/HVBS7] hepatitis B virus integration site 7;

Gene: [18q11/NPC1] intracellular cholesterol transport regulator?; Niemann-Pick disease, type C1 (major form); [NPC ]

Gene: [18q112/CDH2] cadherin 2 (N-cadherin, neural); [NCAD CAHN ]

Gene: [18q112/LAMA3] laminin, alpha 3 (nicein (150kD), kalinin (165kD), BM600 (150kD), epilegrin); epidermolysis bullosa, junctional, Herlitz type (MIM:226700);

Gene: [18q112/SSXT] synovial sarcoma, translocated to X chromosome;

Gene: [18q12/DTNA] dystrobrevin, alpha; dystrophin related protein 3; [DRP3 D18S892E ]

Gene: [18q12/MEP1B] meprin A, beta;

Gene: [18q12/PGDL1] phosphogluconate dehydrogenase-like 1;

Gene: [18q12/SPPK] palmoplantar keratoderma, striated (Brunauer-Fuhs-Siemens) form;

Gene: [18q12/ZNF24] zinc finger protein 24 (KOX 17);

Gene: [18q121/DHFRP1] dihydrofolate reductase pseudogene 1;

Gene: [18q121/DSC1] desmocollin 1a/1b;

Gene: [18q121/DSC3] desmocollin 3a/3b; [DSC2 ]

Gene: [18q121/DSC4] desmocollin 4a/4b;

Gene: [18q121/DSG1] desmoglein 1; [DSG DG1 ]

Gene: [18q121/DSG2] desmoglein 2;

Gene: [18q121/DSG3] desmoglein 3 (pemphigus vulgaris antigen); [PVA ]

Gene: [18q121/PALB] prealbumin, thyroxine-binding (transthyretin); familial amyloidotic polyneuropathy (FAP I/II/III/X); hyperthyroxinemia, dysprealbunemic; [TBPA TTR FAP ]

Gene: [18q122/FRA18A] fragile site 18q12.2, aphidicolin type, common;

Gene: [18q2/CDH7] cadherin 7;

Gene: [18q2/LMAN1] lectin, mannose-binding, 1; intracellular mannose specific lectin; coagulation factor V - factor VIII combined deficiency (MIM:227300); [ERGIC-53 ]

Gene: [18q2/MC4R] melanocortin 4 receptor;

Gene: [18q2/PDB2] Paget disease of bone 2;

Gene: [18q2/TGFBRE] transforming growth factor, beta 1 response element;

Gene: [18q2/TS] thymidylate synthetase (methylenetetrahydrofolate methyltransferase);

Gene: [18q21/CORD1] cone-rod dystrophy 1 (autosomal dominant);

Gene: [18q21/FECH] ferrochelatase (protoporphyria); protoporphyria erythropoietic;

Gene: [18q21/FIC1] familial intrahepatic cholestasis 1; benign recurrent intrahepatic cholestasis (BRIC; MIM:243300); progressive familial intrahepatic cholestasis 1, Byler disease (PFIC1; MIM:211600); [BRIC PFIC1 ]

Gene: [18q21/FVT1] follicular lymphoma variant translocation 1;

Gene: [18q21/IDDM6] insulin-dependent diabetes mellitus 6;

Gene: [18q21/MADH2] MAD (mothers against decapentaplegic, Drosophila) homolog 2; tumor suppressor MADR2 (mutated in colorectal carcinoma); [SMAD2 JV18-1 ]

Gene: [18q21/NARS] asparaginyl-tRNA synthetase;

Gene: [18q211/DCC] suppression of colorectal cancer; colorectal cancer-related sequence in chromosome 18q; tumor suppressor DCC (deleted in colorectal carcinoma); [CRCR1 CRC18 ]

Gene: [18q211/ERVSSA] endogenous retroviral sequence simian sarcoma-associated; simian sarcoma-associated virus 1; gibbon ape leukemia virus-related endogenous retroviral element 1; [SSAV1 ]

Gene: [18q211/MADH4] MAD (mothers against decapentaplegic, Drosophila) homolog 4; pancreatic carcinoma; polyposis, juvenile intestinal (MIM:174900); [SMAD4 DPC4 ]

Gene: [18q213/FEO] expansile osteolysis, familial (McCabe disease); polyostotic osteolytic dysplasia, hereditary expansile; [HEPOD EOF OFE ]

Gene: [18q213/FRA18B] fragile site 18q21.3, aphidicolin type, common;

Gene: [18q213/GRP] gastrin-releasing peptide;

Gene: [18q213/PI5] protease inhibitor 5 (maspin);

Gene: [18q213/SCCA1] squamous cell carcinoma antigen 1; [SCC ]

Gene: [18q213/SCCA2] squamous cell carcinoma antigen 2; protease inhibitor 11 (leucine-serpin); [PI11 ]

Gene: [18q213/YES1] YES proto-oncogene tyrosine kinase; Yamaguchi sarcoma viral homolog 1;

Gene: [18q2133/BCL2] transforming protein BCL-2; B-cell chronic lymphatic leukemia 2 (B-CLL: lymphoma 2);

Gene: [18q221/GTS] Gilles de la Tourette syndrome;

Gene: [18q221/PLGAI2] plasminogen activator inhibitor, type II (placental, arginine-serpin); [PLANH2 PAI2 ]

Gene: [18q221/RANK] receptor activator of nuclear factor-kappa B AF018253;

Gene: [18q23/CBLN2] cerebellin 2;

Gene: [18q23/CYB5] cytochrome b-5 (MIM:123950); methemoglobinemia, type IV, with male pseudohermaphrodism (cytochrome b-5 deficiency);

Gene: [18q23/GALNR1] galanin receptor 1 (brain);

Gene: [18q23/MBP] myelin basic protein;

Gene: [18q23/NFATC1] nuclear factor of activated T-cells, cytoplasmic 1; NFAT transcription complex, cytosolic component; [NF-ATC ]

Gene: [18q23/PEPA] peptidase A;

Gene: [18^/ACTBP3] actin, beta pseudogene 3;

Gene: [18^/ACY1L] aminoacylase 1-like;

Gene: [18^/D18Z1] alphoid satellite DNA from chr 18 (probe pBRHS13);

Gene: [18^/D18Z2] alphoid satellite DNA from chr 18 (probe pYAM4-22);

Gene: [18^/GAPDL11] glyceraldehyde-3-phosphate dehydrogenase-like 11;

Gene: [18^/GGTL1] gamma-glutamyltransferase-like 1;

Gene: [18^/MADH7] MAD (mothers against decapentaplegic, Drosophila) homolog 7; [SMAD7 ]

Gene: [18^/MLTL3] metallothionein-like 3; [MTL3 ]

Gene: [18^/PPIP4] peptidylprolyl cis-trans-isomerase (cyclophilin) pseudogene 4;

Gene: [18^/PTK3B] protein tyrosine kinase PTK3B;

Gene: [18^/RPL17] ribosomal protein L17 (L23);

Gene: [19p1/EXT3] exostoses (multiple) 3;

Gene: [19p1/HHC2] hypocalciuric hypercalcemia 2;

Gene: [19p1/ICAM4] intercellular adhesion molecule 4, Landsteiner-Wiener blood group; LW (Landsteiner-Wiener) blood group; [LW ]

Gene: [19p1/INSL3] insulin-like 3 (Leydig cell);

Gene: [19p1/ITGB1L] integrin, beta 1-like; fibronectin receptor, beta polypeptide-like; [FNRBL ]

Gene: [19p1/UBA52] ubiquitin A-52 residue ribosomal protein fusion product 1;

Gene: [19p1/ZNF121] zinc finger protein 121 (clone ZHC32); [D19S204 ]

Gene: [19p1/ZNF43] zinc finger protein 43 (HTF6);

Gene: [19p1/ZNF53A] zinc finger protein 53A;

Gene: [19p1/ZNF54A] zinc finger protein 54A;

Gene: [19p1/ZNF77] zinc finger protein 77 (pT1);

Gene: [19p1/ZNF90] zinc finger protein 90 (HPF9);

Gene: [19p1/ZNF92] zinc finger protein 92 (HPF12);

Gene: [19p1/ZNF93] zinc finger protein 93 (HPF34);

Gene: [19p12/MEF2B] MADS box transcription enhancer factor 2, polypeptide B; myocyte-specific enhancer factor 2B; [RSRFR2 ]

Gene: [19p12/PAR4] proteinase activated (protease-activated) receptor 4;

Gene: [19p12/ZNF208] zinc finger protein 208;

Gene: [19p12/ZNF209] zinc finger protein 209 (pseudogene);

Gene: [19p12/ZNF85] zinc finger protein 85 (HPF4, HTF1);

Gene: [19p12/ZNF91] zinc finger protein 91 (HPF7, HTF10);

Gene: [19p13/CD70] antigen CD70 (antigen CD27 ligand); [CD27LG ]

Gene: [19p13/CD97] antigen CD97;

Gene: [19p13/CDKN2D] cyclin-dependent kinase inhibitor 2D (p19);

Gene: [19p13/FRA19B] fragile site 19p13, folic acid type, rare;

Gene: [19p13/ICAM3] intercellular adhesion molecule 3 (CDW50); [CDW50 ]

Gene: [19p13/MSK20] antigen MSK20 (glycoprotein 50 kD; monoclonal antibody F10);

Gene: [19p13/MYO1D] myosin ID;

Gene: [19p13/OK] OK blood group; [OKa ]

Gene: [19p13/PIN1] peptidylprolyl cis/trans isomerase, NIMA-interacting 1;

Gene: [19p13/RENT1] regulator of nonsense transcripts 1;

Gene: [19p13/STXBP2] syntaxin binding protein 2; [UNC18B ]

Gene: [19p13/ZNF136] zinc finger protein 136 (clone pHZ-20);

Gene: [19p13/ZNF14] zinc finger protein 14 (KOX 6); [KOX6 ]

Gene: [19p13/ZNF20] zinc finger protein 20 (KOX 13); [KOX13 ]

Gene: [19p131/CACNA1A] calcium channel, voltage-dependent, P/Q type, alpha 1A subunit; calcium channel, L type, alpha 1 polypeptide, isoform 4 (neuroendocrine); migraine, hemiplegic 1 (MIM:141500); spinocerebellar ataxia 6 (MIM:183086); epi

Gene: [19p131/COMP] cartilage oligomeric matrix protein; pseudoachondroplasia (MIM:177170); epiphyseal dysplasia, multiple 1 (Fairbank type; MIM:132400); [PSACH EPD1 ]

Gene: [19p131/EKLF] erythroid Kruppel-like transcription factor;

Gene: [19p131/ELL] eleven-nineteen lysine-rich leukemia gene; RNA polymerase II elongation factor ELL;

Gene: [19p131/IL12RB1] interleukin 12 receptor, beta 1;

Gene: [19p131/JAK3] Janus kinase 3; protein tyrosine kinase JAK3 (leukocyte); immunodeficiency, severe combined;

Gene: [19p131/MELL1] mel transforming oncogene-like 1;

Gene: [19p131/MEL] cell line NK14 derived transforming oncogene; oncogene RAS-family, member rab8 homolog; [RAB8 ]

Gene: [19p131/MYO9B] myosin IXB;

Gene: [19p131/NOTCH3] Notch (Drosophila) homolog 3; cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL; MIM:125310); [CASIL CADASIL ]

Gene: [19p131/PRKACA] protein kinase, cAMP-dependent, catalytic subunit, alpha;

Gene: [19p131/PTGER1] prostaglandin E2 receptor 1 (subtype EP1), 42kD;

Gene: [19p131/RAB3A] oncogene RAS-family, member rab3A;

Gene: [19p131/RFX1] regulatory factor (trans-acting) 1 (influences HLA class II expression); bare lymphocyte syndrome (combined immunodeficiency with lack of HLA-II; MIM:209920); [BLS ]

Gene: [19p131/RPL23AP2] ribosomal protein L23a pseudogene 2;

Gene: [19p131/THRL2] thyroid hormone receptor-like 2; avian leukemia viral homolog-like 2; [ERBAL2 EAR2 ]

Gene: [19p131/TPM4] tropomyosin 4;

Gene: [19p131/ZNF56] zinc finger protein 56;

Gene: [19p131/ZNF66] zinc finger protein 66;

Gene: [19p131/ZNF67] zinc finger protein 67;

Gene: [19p132/ACP5] acid phosphatase 5, tartrate resistant;

Gene: [19p132/ATHS] atherosclerosis susceptibility (lipoprotein associated); atherogenic lipoprotein phenotype (ALP); [ALP ]

Gene: [19p132/BST2] bone marrow stromal cell antigen 2;

Gene: [19p132/CALR] calreticulin; ribonucleoprotein Ro/SS-A; Sjogren syndrome antigen A (autoantigen Ro); [CRTC ]

Gene: [19p132/CNN1] calponin 1, basic, smooth muscle;

Gene: [19p132/CYP4F3] cytochrome P450, subfamily IVF, polypeptide 3;

Gene: [19p132/DNMT1] DNA (cytosine-5-)-methyltransferase 1; DNA methyltransferase 1;

Gene: [19p132/ELAVL1] ELAV (embryonic lethal, abnormal vision, Drosophila)-like 1; Hu antigen R; [HUR ]

Gene: [19p132/EPOR] erythropoietin receptor; erythroleukemia; familial erythrocytosis;

Gene: [19p132/FARSL] phenylalanine-tRNA synthetase-like protein; [CML33 ]

Gene: [19p132/GCDH] glutaryl-CoA dehydrogenase; glutaricaciduria I (glutaryl-CoA dehydrogenase deficiency);

Gene: [19p132/ICAM1] intercellular adhesion molecule 1 (CD54; rhinovirus receptor); [CD54 BB2 ]

Gene: [19p132/ICAM5] intercellular adhesion molecule 5, telencephalin; telencephalin; [TLN TLCN ]

Gene: [19p132/JUNB] protooncogene jun B;

Gene: [19p132/JUND] protooncogene jun D;

Gene: [19p132/LDLR] low density lipoprotein receptor; familial hypercholesterolemia (hyperlipoproteinemia IIA); [HC FH FHC ]

Gene: [19p132/LYL1] lymphoblastic leukemia derived sequence 1;

Gene: [19p132/NAGR1] N-acetyl glucosamine receptor 1 (thyroid);

Gene: [19p132/PRKCSH] protein kinase C substrate 80K-H (glycoprotein 80K-H); [PKCSH G19P1 ]

Gene: [19p132/RAD23A] RAD23 (S. cerevisiae) homolog A; [HHR23A ]

Gene: [19p132/RPS28] ribosomal protein S28;

Gene: [19p132/ST2L] signal transduction protein 2 ligand;

Gene: [19p132/TYK2] tyrosine kinase 2 (fms-like);

Gene: [19p132/U2AF1RS3] U2 small nuclear RNP auxiliary factor 1, 35kD subunit, related subunit 3;

Gene: [19p132/ZNF58] zinc finger protein 58;

Gene: [19p133/AMH] anti-Mullerian hormone (mullerian inhibiting factor); persistent Mullerian duct syndrome, type I (pseudohermaphroditism, male internal; MIM:261550);

Gene: [19p133/ATCAY] ataxia, cerebellar, Cayman type;

Gene: [19p133/AZU1] azurocidin 1; cationic antimicrobial protein (37 kD); [NAZC CAP37 ]

Gene: [19p133/BSG] basigin;

Gene: [19p133/C3] complement component 3; nephritis membranoproliferative with lipodystrophy (C3 deficiency);

Gene: [19p133/CAPS] calcyphosine (canine thyroid regulator homolog);

Gene: [19p133/CDC34] cell division cycle 34; ubiquitin-conjugating enzyme E2-CDC34 complementing;

Gene: [19p133/CIRBP] cold inducible RNA-binding protein; glycine-rich RNA binding protein (cold inducible); [CIRP ]

Gene: [19p133/CSNK1G2] casein kinase 1, gamma 2;

Gene: [19p133/ELA2] elastase 2 (neutrophil?);

Gene: [19p133/EMR1] egf-like module containing, mucin-like, hormone receptor-like sequence 1;

Gene: [19p133/FEB2] febrile convulsions, familial, 2 (MIM:121210);

Gene: [19p133/FUT3] fucosyltransferase 3 (galactoside 3(4)-L-fucosyltransferase); Lewis blood group;

Gene: [19p133/FUT5] fucosyltransferase 5 (alpha (1,3) fucosyltransferase);

Gene: [19p133/FUT6] fucosyltransferase 6 (alpha (1,3) fucosyltransferase);

Gene: [19p133/GAMT] guanidinoacetate N-methyltransferase; guanidinoacetate N-methyltransferase deficiency;

Gene: [19p133/GNA11] guanine nucleotide binding protein (G protein), alpha 11 (Gq class);

Gene: [19p133/GNA15] guanine nucleotide binding protein (G protein), alpha 15 (Gq class);

Gene: [19p133/GTF2F1] general transcription factor IIF, polypeptide 1 (74kD subunit);

Gene: [19p133/GZMM] granzyme M (lymphocyte met-ase 1);

Gene: [19p133/HYL] hematopoietic consensus tyrosine-lacking kinase; protein tyrosine kinase CTK; megakaryocyte-associated tyrosine kinase; leukocyte carboxyl-terminal src kinase related gene;

Gene: [19p133/IGHER2] immunoglobulin E Fc-receptor II (low-affinity; antigen CD23); atopy 4? (allergic asthma and hay fever, liability 4); [CD23A FCE2 ]

Gene: [19p133/INSR] insulin receptor; leprechaunism (Donohue syndrome; MIM:246200);

Gene: [19p133/LMNB2] lamin B2; [LMN2 ]

Gene: [19p133/MA] addressin, mucosal; mucosal addressin cell adhesion molecule 1; [MAdCAM-1 ]

Gene: [19p133/MDRV] muscular dystrophy, with rimmed vacuoles;

Gene: [19p133/MLLT1] myeloid/lymphoid or mixed-lineage leukemia (trithorax (Drosophila) homolog); translocated to, 1; [ENL ]

Gene: [19p133/NDUFS7] NADH dehydrogenase (ubiquinone) Fe-S protein 7 (20kD; NADH-CoQ reductase);

Gene: [19p133/NFIC] nuclear factor I/C, CCAAT-binding transcription factor; [NFI ]

Gene: [19p133/NFIX] nuclear factor I, X-type, CCAAT-binding transcription factor;

Gene: [19p133/NRTN] neurturin;

Gene: [19p133/OAZ] ornithine decarboxylase antizyme;

Gene: [19p133/PGK2] phosphoglycerate kinase 2 (of spermatozoa);

Gene: [19p133/POLR2E] RNA polymerase II (DNA directed) polypeptide E (25kD);

Gene: [19p133/POLRMT] polymerase (RNA) mitochondrial (DNA directed);

Gene: [19p133/PRTN3] proteinase 3 (serineproteinase, neutrophil); Wegener granulomatosis autoantigen;

Gene: [19p133/PSMC1] proteasome (prosome, macropain) 26S subunit, ATPase, 1; 26S protease regulatory subunit 4; [S4 P56 ]

Gene: [19p133/PTPRS] protein tyrosine phosphatase, receptor type, sigma;

Gene: [19p133/RFX2] regulatory factor (trans-acting) 2 (influences HLA class II expression);

Gene: [19p133/SAP62] spliceosome-associated protein;

Gene: [19p133/STK11] serine/threonine kinase 11; Peutz-Jeghers syndrome (MIM:175200);

Gene: [19p133/TBXA2R] thromboxane A2 receptor; bleeding disorder (due to defective thromboxane A2 receptor);

Gene: [19p133/TCF3] transcription factor 3 (E2A immunoglobulin enhancer binding); immunoglobulin enhanser binding factors E12/E47; [E2A ]

Gene: [19p133/TLE1] transducin-like enhancer of split 1, homolog of Drosophila E(spl);

Gene: [19p133/TLE2] transducin-like enhancer of split 2, homolog of Drosophila E(spl);

Gene: [19p133/VAV1] vav 1 oncogene; [VAV ]

Gene: [19p133/ZNF55] zinc finger protein 55;

Gene: [19p133/ZNF57] zinc finger protein 57;

Gene: [19q1/A1BG] alpha-1-B glycoprotein; [GAB ABG ]

Gene: [19q1/CCNE] cyclin E (G1/S-specific);

Gene: [19q1/MANB] mannosidase, alpha B, lysosomal; mannosidosis, alpha- (lysosomal alpha-mannosidase B deficiency);

Gene: [19q1/MSK37] antigen MSK37 (monoclonal antibody S7);

Gene: [19q1/NPHS1] nephrosis 1, congenital, Finnish type; [CNF ]

Gene: [19q1/SYT3] synaptotagmin 3;

Gene: [19q1/ZNF17] zinc finger protein 17 (HPF3, KOX 10); [KOX10 ]

Gene: [19q1/ZNF53B] zinc finger protein 53B;

Gene: [19q1/ZNF78L1] zinc finger protein 78-like 1 (pT3);

Gene: [19q12/UQCRFS1] ubiquinol-cytochrome c reductase, Rieske iron-sulfur polypeptide 1;

Gene: [19q13/AAVS1] adeno-associated virus integration site 1; [AAV ]

Gene: [19q13/BAX] BCL2-associated X protein (apoptosis derepressor);

Gene: [19q13/BLVRB] biliverdin reductase B (EC:1.3.1.24); flavin reductase (NADPH) (EC:1.6.8.2; MIM:601111);

Gene: [19q13/C5R1] complement component 5 receptor 1 (C5a ligand);

Gene: [19q13/DFNA4] deafness, autosomal dominant 4;

Gene: [19q13/E11S] ECHO virus (serotypes 4, 6, 11, 19) sensitivity;

Gene: [19q13/FPRL1] formyl peptide receptor-like 1; lipoxin A4 receptor (formyl peptide receptor related); [LXA4R HM63 ]

Gene: [19q13/FPRL2] formyl peptide receptor-like 2;

Биология и медицина

Gene: [17q2/DDX5] DEAD/H (Asp-Glu-Ala-Asp/His) box polypeptide 5 (RNA helicase, 68kD); RNA-dependent ATPase 1 (nuclear; p68; RNA-helicase 1); — Gene: [19q13/FPRL2] formyl peptide receptor-like 2;

Содержание

Случайный рисунок