Gene: [21q22/KCNE1] potassium voltage-gated channel, Isk-related subfamily, member 1; minimal potassium ion channel (minK); Jervell and Lange-Nielsen syndrome (JLNS; MIM:220400); long QT syndrome (LQTS; LQT5); [IsK minK ] — Gerard ea 1974


  • Gene: [21q22/KCNE1] potassium voltage-gated channel, Isk-related subfamily, member 1; minimal potassium ion channel (minK); Jervell and Lange-Nielsen syndrome (JLNS; MIM:220400); long QT syndrome (LQTS; LQT5); [IsK minK ]
  • Gene: [21q22/NDUFA6] NADH dehydrogenase (ubiquinone) 1 alpha subcomplex, 6 (14kD, B14);
  • Gene: [21q22/PCP4] Purkinje cell protein 4; [PEP-19 ]
  • Gene: [21q22/SH3D1A] SH3 domain protein 1A; [SH3P17 ]
  • Gene: [21q22/SLC5A3] solute carrier family 5 (inositol transporter), member 3; [SMIT ]
  • Gene: [21q22/SON] SON DNA-binding protein;
  • Gene: [21q221/BACH1] BTB and CNC homology, basic leucine zipper transcription factor 1;
  • Gene: [21q221/C21ORF4] plasma transmembrane glycoprotein 4 (chromosome 21, open reading frame 4);
  • Gene: [21q221/GART] trifunctional protein GARS-AIRS-GART; phosphoribosylglycinamide formyltransferase (EC:2.1.2.2); phosphoribosylaminoimidazole synthetase (EC:6.3.3.1); phosphoribosylglycinamide synthetase (EC:6.3.4.13);
  • Gene: [21q221/HLCS] holocarboxylase synthetase (biotin-[proprionyl-Coenzyme A-carboxylase (ATP-hydrolysing)] ligase); multiple carboxylase deficiency, neonatal form;
  • Gene: [21q221/IFNAR1] interferon (alpha, beta and omega) receptor 1; [IFNAR AVP1 ]
  • Gene: [21q221/IFNAR2] interferon (alpha, beta and omega) receptor 2; [IFNBR ]
  • Gene: [21q221/IFNGT1] interferon, gamma transducer 1 (confers antiviral resistance); [IFNGR2 ]
  • Gene: [21q221/KCNJ6] potassium inwardly-rectifying channel, subfamily J, member 6; G-protein coupled potassium inwardly-rectifying channel subfamily, member 2; [KCNJ7 GIRK2 ]
  • Gene: [21q221/SOD1] superoxide dismutase 1, soluble; amyotrophic lateral sclerosis 1 (adult; MIM:105400); indophenoloxidase A;
  • Gene: [21q221/TIAM1] T-cell lymphoma invasion and metastasis 1;
  • Gene: [21q2212/CBR1] carbonyl reductase 1 (NADPH) (EC:1.1.1.184); prostaglandin-E2 9-reductase (EC:1.1.1.189); hydroxyprostaglandin dehydrogenase 15- (NADP+) (EC:1.1.1.197);
  • Gene: [21q222/CAF1A] chromatin assembly factor 1, p60 subunit;
  • Gene: [21q222/DYRK] dual-specificity tyrosine-(Y)-phosphorylation regulated kinase; serine/threonine-specific protein kinase MNB; minibrain (Drosophila) homolog;
  • Gene: [21q222/EZH2] enhancer of zeste (Drosophila) homolog 2;
  • Gene: [21q222/KCNJ15] potassium inwardly-rectifying channel, subfamily J, member 15; [Kir4.2 Kir1.3 ]
  • Gene: [21q222/SIM2] single-minded (Drosophila) homolog 2; [SIM ]
  • Gene: [21q222/TTC3] tetratricopeptide repeat domain 3; [TPRD TPRDI ]
  • Gene: [21q223/ADARB1] adenosine deaminase, RNA-specific, B1 (homolog of rat RED1); double-stranded RNA-specific editase 1; RNA editing enzyme 1;
  • Gene: [21q223/AIRE] autoimmune regulator; autoimmune polyendocrinopathy candidiasis ectodermal dystrophy; polyglandular autoimmune syndrome 1 (Persian-Jewish type); hypoadrenocorticism with hypoparathyroidism and superficial moniliasis; [AP
  • Gene: [21q223/C21ORF1] plasma transmembrane glycoprotein 1 (chromosome 21, open reading frame 1);
  • Gene: [21q223/C21ORF2] plasma transmembrane glycoprotein 2 (chromosome 21, open reading frame 2);
  • Gene: [21q223/C21ORF3] plasma transmembrane glycoprotein 3 (chromosome 21, open reading frame 3);
  • Gene: [21q223/CBFA2] core-binding factor, runt domain, alpha subunit 2 (oncogene Aml1); acute myeloid leukemia 1 (Aml1 oncogene); [AML1 PEBP2A2 ]
  • Gene: [21q223/CBS] cystathionine-beta-synthase; homocystinuria (cystathionine-beta-synthase deficiency);
  • Gene: [21q223/COL18A1] collagen, type XVIII, alpha 1;
  • Gene: [21q223/COL6A1] collagen, type VI, alpha 1; Bethlem myopathy;
  • Gene: [21q223/COL6A2] collagen, type VI, alpha 2; Bethlem myopathy;
  • Gene: [21q223/CRYAA] crystallin, alpha A polypeptide; [CRYA1 ]
  • Gene: [21q223/CSTB] cystatin B (cystatin 6; stefin B); epilepsy, progressive myoclonic 1 (Unverricht-Lundborg type; MIM:254800); [STF2 EPM1 ]
  • Gene: [21q223/DCR] Down syndrome chromosome region; [DSCR ]
  • Gene: [21q223/DFNB8] deafness, autosomal recessive 8; [NSRD8 ]
  • Gene: [21q223/ERG] avian erythroblastosis virus E26 related protein;
  • Gene: [21q223/ETS2] avian erythroblastosis virus E26 homolog 2; acute myeloid leukemia with morphology M2;
  • Gene: [21q223/HES1] ES1 (Zebrafish) homolog; [KNP-I ES1 D21 ]
  • Gene: [21q223/HMG14] high-mobility group (nonhistone chromosomal) protein 14;
  • Gene: [21q223/HPE1] holoprosencephaly 1, alobar;
  • Gene: [21q223/HRMT1L1] HMT1 (hnRNP methyltransferase, S. cerevisiae)-like 1; protein arginine N-methyltransferase 2;
  • Gene: [21q223/IFNIMX1] myxovirus (influenza) resistance 1, homolog of murine; interferon-inducible protein 78; [MX1 MXA ]
  • Gene: [21q223/IFNIMX2] myxovirus (influenza) resistance 2, homolog of murine; interferon-inducible protein 78-related; [MX2 MXB ]
  • Gene: [21q223/ITGB2] integrin, beta 2 (antigen CD18B (p95); LFA1-beta; LCAM-B); cell adhesion molecule, leukocyte, beta (light chain; LCAM-B); lymphocyte function-associated antigen 1, beta subunit (LCAM-B); complement component receptor 3,
  • Gene: [21q223/KNO] Knobloch syndrome (retinal detachment and occipital encephalocele); [KS ]
  • Gene: [21q223/LSS] lanosterol synthase (2,3-epoxysqualene-lanosterol cyclase);
  • Gene: [21q223/NDUFV3] NADH dehydrogenase (ubiquinone) flavoprotein 3 (10kD; EC:1.6.5.3, EC:1.6.99.3);
  • Gene: [21q223/PCNT] pericentrin; [PCN ]
  • Gene: [21q223/PFKL] phosphofructokinase, liver type;
  • Gene: [21q223/PKNOX1] PBX/knotted 1 homeobox 1;
  • Gene: [21q223/PNK] pyridoxal kinase;
  • Gene: [21q223/PWP2] PWP2 (periodic tryptophan protein, S. cerevisiae) homolog; [EHOC-17 PWP2H ]
  • Gene: [21q223/S100B] S100 calcium-binding protein, beta (neural);
  • Gene: [21q223/SH3BGR] SH3 domain binding glutamic acid-rich protein;
  • Gene: [21q223/SLC19A1] solute carrier family 19 (folate transporter), member 1 (placental); [FOLT ]
  • Gene: [21q223/TFF1] trefoil factor 1 (PH1.A); protein pS2 (estrogen-inducible sequence; growth factor); estrogen-inducible sequence, expressed in breast cancer; [BCEI PS2 ]
  • Gene: [21q223/TFF2] trefoil factor 2; spasmolytic protein 1; [SML1 ]
  • Gene: [21q223/TFF3] trefoil factor 3 (PH1.B; intestinal);
  • Gene: [21q223/TMEM1] transmembrane protein 1; [EHOC-1 GT334 ]
  • Gene: [21q223/TMPRSS2] transmembrane protease, serine 2;
  • Gene: [21q223/U2AF1] U2 small nuclear RNP auxiliary factor 1, 35kD subunit; [RNU2AF1 ]
  • Gene: [21q223/WHITE1] white (Drosophila) homolog 1, ATP binding casette transporter superfamily;
  • Gene: [21q223/WRB] tryptophan rich basic protein (nuclear?); congenital heart disease 5 protein (CHD5 protein); congenital heart disease, CHD5-associated; [CHD5 ]
  • Gene: [21^/AABT] beta-amino acid transport;
  • Gene: [21^/ASNSL2] asparagine synthetase-like 2;
  • Gene: [21^/BAS] beta-adrenergic stimulation, response to;
  • Gene: [21^/FDXP2] ferredoxin pseudogene 2 (adrenodoxin pseudogene 2);
  • Gene: [21^/GPXP2] glutathione peroxidase pseudogene 2; [GPXL2 ]
  • Gene: [21^/HSPA3] heat shock 70kD protein 3; [BIP3 ]
  • Gene: [21^/HTOE] 5-hydroxytryptamine (serotonin) oxygenase regulator; [HTOR ]
  • Gene: [21^/NF1L1] neurofibromin 1-like 1 (a processed pseudogene);
  • Gene: [21^/PNY1] protein spot in 2-D gels (MM 82 kD);
  • Gene: [21^/PNY2] protein spot in 2-D gels (MM 65 kD);
  • Gene: [21^/PNY3] protein spot in 2-D gels (MM 33 kD);
  • Gene: [21^/PNY4] protein spot in 2-D gels (MM 72 kD);
  • Gene: [21^/PNY5] protein spot in 2-D gels (MM 40 kD);
  • Gene: [21^/PRKCM] protein kinase C, mu polypeptide;
  • Gene: [21^/PRKCSLL1] protein kinase C substrate 80K-L (myristoylated alanine-rich, MARCKS)-like 1; [MACSL1 ]
  • Gene: [21^/S14] surface antigen S14 (chromosome 21);
  • Gene: [21^/VDAC2] voltage-dependent anion channel 2; outer mitochondrial membrane protein porin 2;
  • Gene: [22p1/D22Z4] satellite DNA, alpha (probe pI90-22);
  • Gene: [22p1/D22Z7] satellite DNA, unknown class (probe N65D4);
  • Gene: [22p1/ZNF72] zinc finger protein 72 (Cos8);
  • Gene: [22p1/ZNF73] zinc finger protein 73 (Cos12);
  • Gene: [22p111/D22Z1] satellite DNA, HinfI subset (probe pM1-4-3);
  • Gene: [22p111/D22Z2] satellite DNA, alpha family (identical to an alpha subset on Chr 13);
  • Gene: [22p111/D22Z3] satellite DNA, HinfI family (48 bp repeat; probe pM1-4-3);
  • Gene: [22p12/D22FB2S1] satellite DNA, beta, NOR5-flanking subset 1; [DNFB2S1 ]
  • Gene: [22p12/D22FB2S2] satellite DNA, beta, NOR5-flanking subset 2; [DNFB2S2 ]
  • Gene: [22p12/RNR5BAM] rDNA subset 5, BamHI-RFLP in downstream 28S rRNA gene (30-50 copies); [RNR5 ]
  • Gene: [22p12/RNR5SN1] RNA, ribosomal 5, 8S-1 RNA (sn-PolI; 30-50 copies); [RNR5 SNPIRNA1 ]
  • Gene: [22p12/RNR5SN2] RNA, ribosomal 5, 8S-2 RNA (sn-PolI; 30-50 copies); [RNR5 SNPIRNA2 ]
  • Gene: [22p12/RNR5UA] RNA, ribosomal 5, accessory unit 5.8S rRNA (30-50 copies); [RNR5 ]
  • Gene: [22p12/RNR5UL] RNA, ribosomal 5, large unit 28S rRNA (30-50 copies); [RNR5 ]
  • Gene: [22p12/RNR5US] RNA, ribosomal 5, small unit 18S rRNA (30-50 copies); [RNR5 ]
  • Gene: [22p13/D22Z5] satellite DNA, unknown class (probe ?);
  • Gene: [22q1/ACO2] aconitase 2, mitochondrial;
  • Gene: [22q1/CRYBA4] crystallin, beta A4 polypeptide;
  • Gene: [22q1/CRYBB2P1] crystallin, beta B2 pseudogene 1; [CRYB2B ]
  • Gene: [22q1/CRYBB2] crystallin, beta B2 polypeptide; cataract, congenital, cerulean type, 2 (MIM:601547); [CRYB2 CRYB2A ]
  • Gene: [22q1/CRYBB3] crystallin, beta B3 polypeptide; [CRYB3 ]
  • Gene: [22q1/CSNK1E] casein kinase 1, epsilon polypeptide;
  • Gene: [22q1/CYP2D7AP] cytochrome P450, subfamily IID (debrisoquine 4-hydroxylase), polypeptide 7a (pseudogene); [CYP2DL1 ]
  • Gene: [22q1/CYP2D7BP] cytochrome P450, subfamily IID (debrisoquine 4-hydroxylase), polypeptide 7b (pseudogene);
  • Gene: [22q1/CYP2D8P] cytochrome P450, subfamily IID (debrisoquine 4-hydroxylase), polypeptide 8 (pseudogene); [CYP2DP1 ]
  • Gene: [22q1/CYP2DL1] cytochrome P450, subfamily IID (debrisoquine 4-hydroxylase) like 1;
  • Gene: [22q1/CYP2DP1] cytochrome P450, subfamily IID (debrisoquine 4-hydroxylase) pseudogene 1;
  • Gene: [22q1/KCNN3] potassium intermediate/small conductance calcium-activated channel, subfamily N, member 3; [SK3 SKCA3 ]
  • Gene: [22q1/LGALS1] lectin, galactoside-binding, soluble, 1; galectin 1 (galaptin; 14.5kD);
  • Gene: [22q1/LGALS2] lectin, galactoside-binding, soluble, 2; galectin 2 (14.65kD);
  • Gene: [22q1/MFNG] manic fringe (Drosophila) homolog;
  • Gene: [22q1/MYH9] myosin, heavy polypeptide 9, non-muscle;
  • Gene: [22q1/NEFH] neurofilament, heavy polypeptide (200kD);
  • Gene: [22q1/P1] P blood group (P1 antigen);
  • Gene: [22q1/PDGFB] platelet-derived growth factor, beta polypeptide; simian sarcoma viral oncogene homolog; [PDGF2 SIS ]
  • Gene: [22q1/PPARA] peroxisome proliferative activated receptor, alpha;
  • Gene: [22q1/PVALB] parvalbumin;
  • Gene: [22q1/RAC2] ras-related C3 botulinum toxin substrate 2; rho family, small GTP binding protein Rac2;
  • Gene: [22q1/SCZD4] schizophrenia disorder 4;
  • Gene: [22q1/SOX10] SRY (sex determining region Y)-box 10; Waardenburg-Hirschsprung disease (MIM:277580); [WS4 ]
  • Gene: [22q1/TCN2] transcobalamin II (vitamin B12 binding protein); vitamin B12 binding deficiency (macrocytic anemia);
  • Gene: [22q1/TIMP3] tissue inhibitor of metalloproteinase 3; Sorsby fundus dystrophy, pseudoinflammatory (MIM:136900);
  • Gene: [22q1/TOP1P2] topoisomerase (DNA) I pseudogene 2;
  • Gene: [22q1/TST] thiosulfate sulfurtransferase (rhodanese);
  • Gene: [22q1/UBE2L3] ubiquitin-conjugating enzyme E2L 3;
  • Gene: [22q11/ADRBK2] adrenergic, beta, receptor kinase 2;
  • Gene: [22q11/ARVCF] armadillo repeat gene deleted in VCFS;
  • Gene: [22q11/CECR] cat eye syndrome chromosome region (Schmid-Fraccaro syndrome); [CES ]
  • Gene: [22q11/CRKL] avian sarcoma virus CT10 (v-crk) oncogene homolog-like;
  • Gene: [22q11/CTHM] cono-truncal heart malformation;
  • Gene: [22q11/DVL] dishevelled (homologous to Drosophila dsh);
  • Gene: [22q11/GGT1] gamma-glutamyltransferase 1 (GGT deficiency); glutathionuria (gamma-glutamyltranspeptidase deficiency);
  • Gene: [22q11/GGT2] gamma-glutamyltransferase 2 (GGT deficiency?); glutathionuria II? (gamma-glutamyltranspeptidase deficiency);
  • Gene: [22q11/GSCL] goosecoid-like homeobox gene;
  • Gene: [22q11/IGKVP3] immunoglobulin kappa subunit, variable region, pseudogene 3;
  • Gene: [22q11/IGKVP4] immunoglobulin kappa subunit, variable region, pseudogene 4;
  • Gene: [22q11/IGKVP5] immunoglobulin kappa subunit, variable region, pseudogene 5;
  • Gene: [22q11/LRE1] LINE retrotransposable element 1;
  • Gene: [22q11/LZTR1] leucine-zipper-like transcriptional regulator 1;
  • Gene: [22q11/MN1] meningioma-associated protein MN1; meningioma chromosome region; [MGCR1 MGCR ]
  • Gene: [22q11/TMVCF] transmembrane protein deleted in velocardiofacial syndrome;
  • Gene: [22q11/TRSPP1] tRNA phosphoserine (opal suppressor), pseudogene 1;
  • Gene: [22q11/ZNF15L2] zinc finger protein 15-like 2 (KOX 8); [KOX8 ]
  • Gene: [22q11/ZNF39L2] zinc finger protein 39-like 2 (KOX 27); [KOX27 ]
  • Gene: [22q111/IGLV1] immunoglobulin lambda subunit, variable region 1; amyloidosis idiopathic (primary)?;
  • Gene: [22q111/IGLV2] immunoglobulin lambda subunit, variable region 2;
  • Gene: [22q112/ADORA2A] adenosine A2a receptor; [ADORA2 RDC8 ]
  • Gene: [22q112/CDC45L] cell division cycle 45, S.cerevisiae, homolog-like; cell division cycle 45-like 2; [CDC45L2 ]
  • Gene: [22q112/CLTD] clathrin, heavy polypeptide (Hd); Di George syndrome (velocardialfacial syndrome); [CLTCL CLH-22 ]
  • Gene: [22q112/COMTE] catechol-O-methyltransferase activity, low (in red cell); [COMT ]
  • Gene: [22q112/CRYBB1] crystallin, beta B1 polypeptide;
  • Gene: [22q112/DGCR2] DiGeorge critical region gene 2; integral membrane protein, deleted in DiGeorge syndrome; [IDD ]
  • Gene: [22q112/DGCR6] DiGeorge critical region gene 6;
  • Gene: [22q112/DGCR] DiGeorge syndrome chromosome region; DiGeorge syndrome (hypoplasia of thymus and parathyroids); velocardiofacial syndrome (conotruncal anomaly face syndrome; MIM:192430); [DGS CATCH22 ]
  • Gene: [22q112/F8VWFP] coagulation factor VIII VWF (von Willebrand factor) pseudogene; [VWFP ]
  • Gene: [22q112/GNAZ] guanine nucleotide binding protein (G protein), alpha z polypeptide;
  • Gene: [22q112/GP1BB] glycoprotein Ib (platelet), beta polypeptide;
  • Gene: [22q112/GSTT1] glutathione S-transferase T1 (theta class);
  • Gene: [22q112/GSTT2] glutathione S-transferase T2 (theta class);
  • Gene: [22q112/HCF2] heparin cofactor II (thrombophilia); thrombophilia due to heparin cofactor II deficiency; [HC2 ]
  • Gene: [22q112/HIRA] HIR (histone cell cycle regulation defective, S. cerevisiae) homolog A; Tup-like enhancer of split 1; [TUPLE1 ]
  • Gene: [22q112/IGLVL1] immunoglobulin variable region related pre-B cell peptide 1; immunoglobulin lambda-like polypeptide 1; agammaglobulinaemia, autosomal recessive; [IGL5 VPREB1 ]
  • Gene: [22q112/IGLVL2] immunoglobulin variable region related pre-B cell peptide 2; immunoglobulin lambda-like polypeptide 2; [IGLL2 VPREB2 ]
  • Gene: [22q112/IGLVL3] immunoglobulin variable region related pre-B cell peptide 3; immunoglobulin lambda-like polypeptide 3; [IGLL3 ]
  • Gene: [22q112/MIF] macrophage migration inhibitory factor; glycosylation-inhibiting factor; phenylpyruvate tautomerase;
  • Gene: [22q112/MMP11] matrix metalloproteinase 11; stromelysin 3; breast cancer progression;
  • Gene: [22q112/PNUTL1] peanut-like 1 (Drosophila homolog; GTPase-like?); cell division cycle-related; [CDCREL ]
  • Gene: [22q112/PRKM1] protein kinase, mitogen-activated 1; MAP kinase 1 (p40, p41); extracellular signal-regulated kinase 2 (p42);
  • Gene: [22q112/PRODH] proline dehydrogenase (proline oxidase); hyperprolinemia, type I (proline oxidase deficiency);
  • Gene: [22q112/TBX1] T-box 1;
  • Gene: [22q112/UFD1L] ubiquitin fusion degradation 1-like protein;
  • Gene: [22q112/YESP] Yamaguchi sarcoma viral homolog, pseudogene; [YES2 SYR SYN ]
  • Gene: [22q112/ZNF69] zinc finger protein 69 (Cos5);
  • Gene: [22q112/ZNF70] zinc finger protein 70 (Cos17);
  • Gene: [22q112/ZNF71] zinc finger protein 71 (Cos26);
  • Gene: [22q112/ZNF74] zinc finger protein 74 (Cos52);
  • Gene: [22q1121/BCR2] breakpoint cluster region 2; [BCRL2 ]
  • Gene: [22q1121/BCR4] breakpoint cluster region 4; [BCRL4 ]
  • Gene: [22q1121/IGLC1] immunoglobulin lambda subunit, constant region 1;
  • Gene: [22q1121/IGLC2] immunoglobulin lambda subunit, constant region 2;
  • Gene: [22q1121/IGLC3] immunoglobulin lambda subunit, constant region 3;
  • Gene: [22q1121/IGLC6] immunoglobulin lambda subunit, constant region 6;
  • Gene: [22q1121/IGLCP1] immunoglobulin lambda subunit, constant region, pseudogene 1; [IGLC4 IGLP1 ]
  • Gene: [22q1121/IGLCP2] immunoglobulin lambda subunit, constant region, pseudogene 2; [IGLC5 ]
  • Gene: [22q1121/IGLJ1] immunoglobulin lambda subunit, J-1 segment;
  • Gene: [22q1121/IGLJ2] immunoglobulin lambda subunit, J-2 segment;
  • Gene: [22q1121/IGLJ3] immunoglobulin lambda subunit, J-3 segment;
  • Gene: [22q1121/IGLJ6] immunoglobulin lambda subunit, J-6 segment;
  • Gene: [22q1121/IGLJP1] immunoglobulin lambda subunit, J-4 segment, pseudogene 1?;
  • Gene: [22q1121/IGLJP2] immunoglobulin lambda subunit, J-4 segment, pseudogene 2?;
  • Gene: [22q1121/SLC20A3] solute carrier family 20 (mitochondrial citrate transporter), member 3; tricarboxylate transport protein, mitochondrial; [CTP ]
  • Gene: [22q1122/BCR1] breakpoint cluster region 1; chronic myelogenous leukemia (CML; Ph'-oncomarker); [PHL BCR ]
  • Gene: [22q1123/BCR3] breakpoint cluster region 3; [BCRL3 ]
  • Gene: [22q12/ADTB1] adaptin, beta 1 (beta prime); meningioma-associated locus BAM22; [BAM22 AP105A ]
  • Gene: [22q12/CAMK2B] calcium/calmodulin-dependent protein kinase (CaM kinase) 2 beta;
  • Gene: [22q12/GAR22] GAR22 protein (GAS2-related on chromosome 22);
  • Gene: [22q12/HMOX1] heme oxygenase (decycling) 1;
  • Gene: [22q12/LIF] leukemia inhibitory factor (differentiation-stimulating); [HILDA ]
  • Gene: [22q12/LIMK2] LIM domain kinase 2; LIM motif-containing protein kinase 2;
  • Gene: [22q12/MB] myoglobin;
  • Gene: [22q12/NIPSNAP1] 4-nitrophenylphosphatase domain and nonneuronal snap25-like 1; [NIPSNAP1 ]
  • Gene: [22q12/OSM] oncostatin M;
  • Gene: [22q12/RFPL1ANT] ret finger protein-like 1 antisense; [RFPL1S ]
  • Gene: [22q12/RFPL1] ret finger protein-like 1; [rfpl1l rfpl1s ]
  • Gene: [22q12/RFPL2] ret finger protein-like 2;
  • Gene: [22q12/RFPL3ANT] ret finger protein-like 3 antisense; [RFPL3S ]
  • Gene: [22q12/RFPL3] ret finger protein-like 3;
  • Gene: [22q12/RRP22] RAS-like protein RRP22 (RAS-related on chromosome 22);
  • Gene: [22q12/SMTN] smoothelin;
  • Gene: [22q12/YWHAH] tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, eta polypeptide; protein kinase C-dependent activator of tyrosine/tryptophan hydroxylase; brain protein 14-3-3, eta subtype; [YWHA1 AS1 ]
  • Gene: [22q121/EWSR1] Ewing sarcoma breakpoint region 1 (peripheral neuroepithelioma 1); Askin tumor (esthesioneuroblastoma); [EWS ES ]
  • Gene: [22q122/FRA22B] fragile site 22q12.2, aphidicolin type, common;
  • Gene: [22q122/NF2] neurofibromin 2; merlin (schwannomin); neurofibromatosis 2 (bilateral acoustic neurinoma); [BANF ]
  • Gene: [22q13/ACR] acrosin (sperm head acrosomal endoprotease);
  • Gene: [22q13/FRA22A] fragile site 22q13, folic acid type, rare;
  • Gene: [22q13/GAD3] glutamate decarboxylase 3;
  • Gene: [22q13/IL2RB] interleukin 2 receptor, beta (low affinity; p70-75; antigen CD122); [GP75 NONTAC ]
  • Gene: [22q13/MCM5] minichromosome maintenance deficient (S.cerevisiae) 5; cell division cycle 46 (homologous to CDC46 of S. cerevisiae); DNA replication licensing factor MCM5; [CDC46 ]
  • Gene: [22q13/NAGA] acetylgalactosaminidase, alpha-N- (alpha-galactosidase B); Schindler neuroaxonal dystrophy (alpha-galactosidase deficiency);
  • Gene: [22q13/RPL3] ribosomal protein L3;
  • Gene: [22q13/SREBF2] sterol regulatory element binding transcription factor 2;
  • Gene: [22q13/TAKU] thyroid autoantigen, 70kD (antigen Ku; p70; lupus antigen); ATP-dependent DNA helicase II, 70kD;
  • Gene: [22q13/TEF] thyrotrophic embryonic factor;
  • Gene: [22q13/UQCRFSL1] ubiquinol-cytochrome c reductase, Rieske iron-sulfur polypeptide-like 1;
  • Gene: [22q131/ADSL] adenylosuccinate lyase; autism, succinylpurinemic (adenylosuccinase deficiency);
  • Gene: [22q131/CSF2RB] colony stimulating factor 2 receptor, beta, low-affinity (granulocyte-macrophage); granulocyte-macrophage factor CSF2 receptor, beta; interleukin 3 receptor, beta; interleukin 5 receptor, beta; pulmonary alveolar prote
  • Gene: [22q131/CYP2D6] cytochrome P450, subfamily IID (debrisoquine 4-hydroxylase), polypeptide 6; debrisoquine/sparteine polymorphism;
  • Gene: [22q131/GGT3] gamma-glutamyltransferase 3;
  • Gene: [22q131/H1F0] H1 histone family, member 0; [H1FV ]
  • Gene: [22q131/KCNJ4] potassium inwardly-rectifying channel, subfamily J, member 4;
  • Gene: [22q131/MGAT3] mannosyl (beta-1,4-)-glycoprotein beta-1,4-N-acetylglucosaminyltransferase;
  • Gene: [22q131/NCF4] neutrophil cytosolic factor 4 (40kD); [p40phox ]
  • Gene: [22q131/PLA2G6] phospholipase A2, group VI;
  • Gene: [22q131/PMM1] phosphomannomutase 1;
  • Gene: [22q131/SLC5A1] solute carrier family 5 (sodium/glucose transporter), member 1 (intestinal); congenital glucose-galactose malabsorbtion syndrome; [SGLT1 ]
  • Gene: [22q131/SSTR3] somatostatin receptor 3;
  • Gene: [22q133/ARSA] arylsulfatase A (metachromatic leukodystrophy); metachromatic leukoencephalopathy (leukodystrophy); cerebral sclerosis, diffuse, metachromatic form (ARS-A deficiency); sulfatide lipidosis (ARS-A deficiency);
  • Gene: [22q133/BZRP] benzodiazepine receptor (peripheral);
  • Gene: [22q133/CELSR1] cadherin EGF LAG seven-pass G-type receptor;
  • Gene: [22q133/CHKL] choline kinase-like;
  • Gene: [22q133/CPT1B] carnitine palmitoyltransferase I, muscle;
  • Gene: [22q133/DIA1] diaphorase 1 (NADH) (cytochrome b-5 reductase); methemoglobinemia (cytochrome b-5 reductase deficiency);
  • Gene: [22q133/ECGF1] endothelial cell growth factor 1 (platelet-derived); thymidine phosphorylase;
  • Gene: [22q133/FBLN1] fibulin 1; [FBLN ]
  • Gene: [22q133/GPR24] G protein-coupled receptor 24 (somatostatin receptor-like); [SLC SSTR ]
  • Gene: [22q133/SAPK3] stress-activated SAPK/Erk protein kinase 3; protein kinase, mitogen-activated 12;
  • Gene: [22q133/WNT7B] wingless-type MMTV integration site 7B, human homolog;
  • Gene: [22^/ASLL] argininosuccinate lyase-like; [ASLP ]
  • Gene: [22^/ATP6E] ATPase, H+ transporting, lysosomal (vacuolar proton pump) 31kD;
  • Gene: [22^/BP239A] adult brain protein 239; [239AB C22orf1 ]
  • Gene: [22^/COX5BL7] cytochrome c oxidase subunit Vb-like 7;
  • Gene: [22^/HBQP] hemoglobin, theta pseudogene;
  • Gene: [22^/MSK40] antigen MSK40 (monoclonal antibody F35/9; gp45);
  • Gene: [22^/MSK41] antigen MSK41 (monoclonal antibody E3);
  • Gene: [22^/NRASL2] neuroblastoma ras viral homolog-like 2;
  • Gene: [22^/S13] surface antigen S13 (chromosome 22);
  • Gene: [22^/XBP1] X-box binding protein 1; [XBP2 ]
  • Gene: [ADH/04q22] alcohol dehydrogenase, gene cluster 4q22; (ADH1 ADH2 ADH3 ADH4 ADH5 ADH5P1)
  • Gene: [ALP/02q37] alkaline phosphatase gene cluster 2q37; (ALPIA ALPIF ALPPR ALPT)
  • Gene: [AMY/01p21] amylase; (AMY1A AMY1B AMY1C AMY2A AMY2B AMYP1)
  • Gene: [APOAC/11q233] apolipoproteins, gene cluster APOAC (in chr 11q2); (APOA1 APOA4 APOC3)
  • Gene: [APOCE/19q132] apolipoproteins, gene cluster APOCE (in chr 19q132); (APOC1 APOC1P1 APOC2 APOC4 APOE)
  • Gene: [BAT/06p2133] HLA-B-associated gene family; (BAT1 BAT2 BAT3 BAT4 BAT5 LST1)
  • Gene: [CD1/01q2] antigen CD1; (CD1A CD1B CD1C CD1D CD1E)
  • Gene: [CD8/02p12] antigen CD8 (cluster on chr 2); (CD8A CD8B1 CD8B2)
  • Gene: [CRYG/02q3] crystallin, gamma, gene cluster in Chr 2q3; (CRYGA CRYGB CRYGC CRYGD CRYGEP1 CRYGFP1 CRYGGP1 CRYGP1 CRYGP2)
  • Gene: [CSN/04q211] caseins; (CSN1 CSN2 CSN10)
  • Gene: [CST/20p112] cystatins; (CST1 CST2 CST3 CST4 CST5 CSTP1 CSTP2)
  • Gene: [CYP11B/08q21] cytochrome P450, subfamily XIB in chr 8q21; (CYP11B1 CYP11B2)
  • Gene: [CYP21/06p2133] cytochrome P450, subfamily XXI in chr 6p2133; (CYP21 CYP21P)
  • Gene: [CYP2ABF/19q132] cytochrome P450, subfamily II in Chr 19q13.2; (CYP2A6 CYP2A7 CYP2A7P1 CYP2A7P2 CYP2A13 CYP2B6 CYP2B7 CYP2B8 CYP2F1)
  • Gene: [CYP2C/10q241] cytochrome P450, subfamily IIC in Chr 10q24.1; (CYP2C8 CYP2C9 CYP2C10 CYP2C18 CYP2C19)
  • Gene: [CYP2D/22q1] cytochrome P450, subfamily IID in chr 22q1; (CYP2D6 CYP2D7AP CYP2D7BP CYP2D8P CYP2DL1 CYP2DP1)
  • Gene: [CYP3/07q2] cytochrome P450 gene family in chr 7q2; (CYP3A3 CYP3A4 CYP3A5 CYP3A7)
  • Gene: [CYPCHR10/10q24] cytochrome P450 gene family in chr 10q24; (@CYP2C CYP2E1 CYP17)
  • Gene: [CYPCHR15/15q2] cytochrome P450 gene family in chr 15q2; (CYP1A1 CYP1A2 CYP11A CYP19)
  • Gene: [F1/04q28] fibrinopeptides, gene cluster 4q28; (F1A F1B F1G)
  • Gene: [FOLR/11q13] folate receptors; (FOLR1 FOLR1P FOLR2 FOLR2L FOLR3)
  • Gene: [FRA/00.0] fragile chromosome sites superfamily; (@FRAAZ @FRABR @FRADA @FRAFA @FRAUN)
  • Gene: [FRAAZ/00.0] fragile azacytidine sites family; (FRA1J FRA1H FRA9F)
  • Gene: [FRABR/00.0] fragile BrdU-type sites family; (FRA4B FRA5A FRA5B FRA6D FRA9C FRA10B FRA10C FRA12C FRA13B)
  • Gene: [FRADA/00.0] fragile distamycin sites family; (FRA8E FRA11I FRA16B FRA16E FRA17A)
  • Gene: [FRAFA/00.0] fragile folic acid sites family; (FRA2A FRA2B FRA2K FRA6A FRA7A FRA8A FRA9A FRA9B FRA10A FRA11A FRA11B FRA12A FRA12D FRA16A FRA19B FRA20A FRA22A FMR1)
  • Gene: [FRAUN/00.0] fragile unclassified sites family; (FRA4E FRA8F FRAYA)
  • Gene: [GHCS/17q2] growth-hormone gene family; (CSH1 CSH2 CSHP1 GH1 GH2)
  • Gene: [HBA/16p133] hemoglobin, alpha-polypeptide gene family; (HBA1 HBA2 HBA3 HBAP1 HBAP2 HBHR HBQ1 HBZ HBZP HVRDQ HVRIZ HVRUZ)
  • Gene: [HBB/11p155] hemoglobin, beta- and associated loci; (HBB HBBP HBD HBE HBG1 HBG2 HBGR HBHPAI HPFH1)
  • Gene: [HIS1/07q] histone multigene family cluster 7q; (H2A1 H2B1 H3F1 H4F1)
  • Gene: [HIS2/01q21] histone multigene family cluster 1q21; (H1F2 H2A2 H2B2 H3F2 H4F2)
  • Gene: [HOXA/07p1] homeo box region A, gene cluster on chr 7p1; (HOXA1 HOXA2 HOXA3 HOXA4 HOXA5 HOXA6 HOXA7 HOXA9 HOXA10 HOXA11 HOXA13)
  • Gene: [HOXB/17q2] homeo box region B, gene cluster on chr 17q2; (HOXB1 HOXB2 HOXB3 HOXB4 HOXB5 HOXB6 HOXB7 HOXB8 HOXB9 HOXB13)
  • Gene: [HOXC/12q1] homeo box region C, gene cluster on chr 12q1; (HOXC4 HOXC5 HOXC6 HOXC8 HOXC9 HOXC10 HOXC11 HOXC12 HOXC13)
  • Gene: [HOXD/02q31] homeo box region D, gene cluster on chr 2q31; (HOXD1 HOXD3 HOXD4 HOXD8 HOXD9 HOXD10 HOXD11 HOXD12 HOXD13)
  • Gene: [HPH/20] hypothalamic peptide hormones; (ARVP OT)
  • Gene: [IFN9/09p22] interferon genes' cluster on chromosome 9p; (@IFNA IFNB1 @IFNW IFNP24)
  • Gene: [IFNAS/09p22] interferon, class alpha-S polypeptides (mRNA 0.7-1.4 kb); (IFNAS1 IFNAS2 IFNAS3 IFNAS4 IFNAS5 IFNAS6 IFNAS7 IFNAS8 IFNAS9 IFNAS10 IFNAS11 IFNAS12 IFNAS13 IFNAS14 IFNAS16 IFNAS17 IFNAS21 IFNAP22 IFNASP1A IFNASP1B IFNASP2)
  • Gene: [IFNW/09p22] interferon, omega; (IFNW1 IFNWP9 IFNWP15 IFNWP18 IFNWP19)
  • Gene: [IGH/14q3233] immunoglobulin, heavy subunit, CON-J-DIV-VAR minigenes; (@IGHC @IGHDIV @IGHJ @IGHV)
  • Gene: [IGHC/14q3233] immunoglobulin, heavy subunit, constant region genes; (IGHA1 IGHA2 IGHG1 IGHG2 IGHG3 IGHG4 IGHD IGHE IGHM IGHMAS)
  • Gene: [IGHDIV/14q3233] immunoglobulin heavy chain, diversity region minigenes; (IGHDYA1 IGHDYA2 IGHDYA3 IGHDYA4 IGHDYA5 IGHDYA6 IGHDYA7 IGHDYA8 IGHDYA9 IGHDYA10 IGHDYB1 IGHDYB2)
  • Gene: [IGHJ/14q3233] immunoglobulin, heavy subunit, J-segment genes; (IGHJ1 IGHJ2 IGHJ3 IGHJ4 IGHJ5 IGHJ6 IGHJP1 IGHJP2 IGHJP3)
  • Gene: [IGHV/14q3233] immunoglobulin, heavy chain, variable minigenes, I-VI classes; (IGHVP1 IGHVA1 IGHVB1 IGHVC1 IGHVD1 IGHVE1 IGHVF1)
  • Gene: [IGK/02p12] immunoglobulin, kappa polypeptides, gene claster; (IGKC IGKJ1 IGKJ2 IGKJ3 IGKJ4 IGKJ5 @IGKV)
  • Gene: [IGKV/02p12] immunoglobulin, kappa VAR-polypeptides, minigene cluster; (IGKV4F1 @IGKVA @IGKVL IGKVO9 IGKVO10 IGKVW1)
  • Gene: [IGKVA/02p12] immunoglobulin, kappa VAR-polypeptides, minigene A-cluster; (IGKVA1 IGKVA2 IGKVA3 IGKVA7 IGKVA8 IGKVA9 IGKVA10 IGKVA11 IGKVA13 IGKVA14 IGKVA17 IGKVA18 IGKVA19 IGKVA23 IGKVA24 IGKVA25 IGKVA26 IGKVA27 IGKVA29 IGKVA30 IGKVA
  • Gene: [IGKVL/02p12] immunoglobulin, kappa VAR-polypeptides, minigene L-cluster; (IGKVL1 IGKVL3 IGKVL4 IGKVL6 IGKVL7 IGKVL8 IGKVL9 IGKVL10 IGKVL12 IGKVL13 IGKVL15 IGKVL16 IGKVL17 IGKVL18 IGKVLP1 IGKVLP2 IGKVLP3 IGKVLP4)
  • Gene: [IGL/22q11] immunoglobulin lambda subunit, variable region; (@IGLCJ IGLV1 IGLV2 IGLVL1 IGLVL2 IGLVL3)
  • Gene: [IGLCJ/22q1121] immunoglobulin lambda subunit, constant region and J-segments; (IGLC1 IGLC2 IGLC3 IGLC6 IGLCP1 IGLCP2 IGLJ1 IGLJ2 IGLJ3 IGLJ6 IGLJP1 IGLJP2)
  • Gene: [MDR/07q211] multidrug-resistance complex, gene family; (PGY1 PGY1P PGY3 SRI)
  • Gene: [MHC/06p2133] major histocompatibility complex; cell-surface MHC-glycoproteins; (@MHC1 @MHC3 @MHC2)
  • Gene: [MHC1/06p2133] major histocompatibility complex, MHC, class I polypeptides; (HLAA HLAB HLAC HLAE HLAF HLAG HLAH HLAJ HLAK HLAL)
  • Gene: [MHC2/06p2133] major histocompatibility complex, class II polypeptides; (HLADRA HLADRB1 HLADRB1L HLADRB2 HLADRB2P HLADRB3 HLADRB4 HLADRB5 HLADRB6 HLADRB7 HLADRB8 HLADRB9 HLADMA HLADMB HLADQA1 HLADQB1 HLADVB HLADQA2 HLADQB2 HLADQB3 HLA
  • Gene: [MHC3/06p2133] major histocompatibility complex, MHC, class III polypeptides; (@BAT TNFB TNFA C2 BF C4A C4B MICA MICB MICC MICD MICE G11)
  • Gene: [MLT1/16q13] metallothioneins, gene cluster in chr 16q13; (MLT1A MLT1B MLT1CP MLT1DP MLT1E MLT1F MLT1G MLT1H MLT1I MLT1J MLT1K MLT1L MLT1X MLT2A MLT3)
  • Gene: [RCA/01q32] complement activation regulator proteins; (CR1 CR2 C4BPA C4BPAL1 C4BPAL2 C4BPB DAF HF1 HFL3 HF2 MCP MCPL)
  • Gene: [RNR05S/01q4213] RNA, 5S, cluster; (RNR05S RNR05SP1 RNR05SP2 RNR05SP3 RNR05SP4)
  • Gene: [RNR1/13p12] rRNA, rDNA tandem 1 (8S-18S-5.8S-28S rRNA genes); (RNR1BAM RNR1SN1 RNR1SN2 RNR1UA RNR1UL RNR1US)
  • Gene: [RNR2/14p12] rRNA, rDNA tandem 2 (8S-18S-5.8S-28S rRNA genes); (RNR2BAM RNR2SN1 RNR2SN2 RNR2UA RNR2UL RNR2US)
  • Gene: [RNR3/15p12] rRNA, rDNA tandem 3 (8S-18S-5.8S-28S rRNA genes); (RNR3BAM RNR3SN1 RNR3SN2 RNR3UA RNR3UL RNR3US)
  • Gene: [RNR4/21p12] rRNA, rDNA tandem 4 (8S-18S-5.8S-28S rRNA genes); (RNR4BAM RNR4SN1 RNR4SN2 RNR4UA RNR4UL RNR4US)
  • Gene: [RNR5/22p12] rRNA, rDNA tandem 5 (8S-18S-5.8S-28S rRNA genes); (RNR5BAM RNR5SN1 RNR5SN2 RNR5UA RNR5UL RNR5US)
  • Gene: [S100A/01q21] S100 calcium-binding protein, A subunit; (S100A1 S100A2 S100A3 S100A4 S100A5 S100A6 S100A7 S100A8 S100A9 S100A10 S100A11 S100A12 S100A13)
  • Gene: [SPF12P/12p132] salivary proteins cluster on chr 12p; (SPFCON1 SPFCON2 SPFGR1 SPFGR2 @SPFPR SPFUC SPFUO SPFUS)
  • Gene: [SPFPR/12p132] salivary protein complex, proline rich polypeptide; (SPFPRB1 SPFPRB2 SPFPRB3 SPFPRB4 SPFPRH1 SPFPRH2)
  • Gene: [SPRR/01q21] small proline-rich proteins; (SPRR1A SPRR1B SPRR2A SPRR2B SPRR2C SPRR2D SPRR2E SPRR2F SPRR2G SPRR3)
  • Gene: [SURF/09q341] surfeits; (SURF1 SURF2 RPL7A SURF4 SURF5 SURF6)
  • Gene: [TCR1A/14q112] T cell receptor, Ti-alpha polypeptide; TiT3 receptor complex, Ti-alpha polypeptide; (TCR1AC TCR1ADY TCR1AJ TCR1AV)
  • Gene: [TCR1AD/14q112] T cell receptor, Ti-alpha/delta polypeptides; TiT3 receptor complex, Ti-alpha/delta polypeptides; (@TCR1A @TCR1D)
  • Gene: [TCR1B/07q35] T cell receptor, Ti-beta polypeptide; (@TCR1BNV @TCR1BV)
  • Gene: [TCR1BG/07] T cell receptor, Ti-beta/gamma polypeptide family; (@TCR1B @TCR1G)
  • Gene: [TCR1BNV/07q35] T cell receptor, Ti-beta polypeptide CON/DIV/J-region; (TCR1B1C TCR1B1D TCR1B1J1 TCR1B1J2 TCR1B1J3 TCR1B1J4 TCR1B1J5 TCR1B1J6 TCR1B2C TCR1B2D TCR1B2J1 TCR1B2J2 TCR1B2J3 TCR1B2J4 TCR1B2J5 TCR1B2J6 TCR1B2J7)
  • Gene: [TCR1BV/07q35] T cell receptor, Ti-beta subunit, VAR-region; (TCR1BV1 TCR1BV2 TCR1BV3 TCR1BV4 TCR1BV5 TCR1BV6 TCR1BV7 TCR1BV8 TCR1BV9 TCR1BV10 TCR1BV11 TCR1BV12 TCR1BV13 TCR1BV14 TCR1BV15 TCR1BV16 TCR1BV17 TCR1BV18 TCR1BV19 TCR1BV20 T
  • Gene: [TCR1D/14q112] T cell receptor, Ti-delta polypeptide; TiT3 receptor complex, Ti-delta polypeptide; (TCR1DC TCR1DJ1 TCR1DJ2)
  • Gene: [TCR1G/07p15] T cell receptor, Ti-gamma polypeptide; T cell rearranging gene, gamma; (TCR1GC1 TCR1GC2 TCR1GJ1 TCR1GJ2 TCR1GJP0 TCR1GJP1 TCR1GJP2 @TCR1GV)
  • Gene: [TCR1GV/07p15] T cell receptor, Ti-gamma subunit, VAR-region; (TCR1GV1P TCR1GV2 TCR1GV3 TCR1GV4 TCR1GV5 TCR1GV5P TCR1GV6P TCR1GV7P TCR1GV8 TCR1GV9 TCR1GV9P TCR1GV10 TCR1GVTP TCR1GV11)
  • Gene: [TCR2DEG/11q233] T cell TiT3 receptor complex, signal component T3(CD3); (TCR2D TCR2E TCR2G)
  • Gene: [TCRBV/09p] T-cell receptor, beta variable region, orphan; (TCRBV2O TCRBV4O TCRBV10O TCRBV11O TCRBV15O)
  • Gene: [TRNA14/14q112] tRNA cluster in Chr 14q11.2; (TRL1 TRK1 TRL2 TRQ1 TRR1)
  • Gene: [TRNA17/17p131] tRNA cluster in Chr 17p13.1; (TRG2 TRK1 TRL2 TRQ1 TRR1)
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