Gene: [0X^/ECHD] enoyl-CoA hydratase (3-hydroxyacyl-CoA hydro-lyase); — Gene: [11p15/PDE3B] phosphodiesterase 3B, cGMP-inhibited; cyclic-AMP phosphodiesterase, adipocyte, cGMP-inhibited;

  • Gene: [0X^/ECHD] enoyl-CoA hydratase (3-hydroxyacyl-CoA hydro-lyase);
  • Gene: [0X^/EEF1B4] eukaryotic translation elongation factor 1 beta 4;
  • Gene: [0X^/F2L] coagulation factor II (prothrombin)-like;
  • Gene: [0X^/GAPDL10] glyceraldehyde-3-phosphate dehydrogenase-like 10;
  • Gene: [0X^/GAPDL2] glyceraldehyde-3-phosphate dehydrogenase-like 2;
  • Gene: [0X^/GPXP1] glutathione peroxidase pseudogene 1; [GPXL1 ]
  • Gene: [0X^/HSPAP1] heat shock 70kD protein, pseudogene 1;
  • Gene: [0X^/HSPBL3] heat shock 27kD protein-like 3;
  • Gene: [0X^/IHG1] iris hypoplasia with glaucoma 1; [IHG ]
  • Gene: [0X^/IL13RA1] interleukin 13 receptor, alpha 1; [NR4 ]
  • Gene: [0X^/KRT18L1] keratin 18-like 1;
  • Gene: [0X^/LDHBP] lactate dehydrogenase B pseudogene; [LDHBL2 ]
  • Gene: [0X^/LUSX] Lutheran supressor, X-linked (supressor of Lu antigens); [XS ]
  • Gene: [0X^/MAA] microphthalmia or anophthalmia and associated anomalies;
  • Gene: [0X^/MEAX] myopathy with excessive autophagy; [XMEA ]
  • Gene: [0X^/MF4] metacarpal 4-5 fusion;
  • Gene: [0X^/MRX10] mental retardation, X-linked 10;
  • Gene: [0X^/MRX11] mental retardation, X-linked 11;
  • Gene: [0X^/MRX12] mental retardation, X-linked 12;
  • Gene: [0X^/MRX13] mental retardation, X-linked 13;
  • Gene: [0X^/MRX14] mental retardation, X-linked 14;
  • Gene: [0X^/MRX16] mental retardation, X-linked 16;
  • Gene: [0X^/MRX17] mental retardation, X-linked 17;
  • Gene: [0X^/MRX18] mental retardation, X-linked 18;
  • Gene: [0X^/MRX1] mental retardation, X-linked 1 (non-dysmorphic);
  • Gene: [0X^/MRX26] mental retardation, X-linked 26;
  • Gene: [0X^/MRX31] mental retardation, X-linked 31;
  • Gene: [0X^/MRX34] mental retardation, X-linked 34;
  • Gene: [0X^/MRX36] mental retardation, X-linked 36;
  • Gene: [0X^/MRX39] mental retardation, X-linked 39;
  • Gene: [0X^/MRX42] mental retardation, X-linked 42;
  • Gene: [0X^/MRX43] mental retardation, X-linked 43;
  • Gene: [0X^/MRX44] mental retardation, X-linked 44;
  • Gene: [0X^/MRX45] mental retardation, X-linked 45;
  • Gene: [0X^/MRX46] mental retardation, X-linked 46;
  • Gene: [0X^/MRX51] mental retardation, X-linked 51;
  • Gene: [0X^/MRX52] mental retardation, X-linked 52;
  • Gene: [0X^/MRX54] mental retardation, X-linked 54;
  • Gene: [0X^/MRX55] mental retardation, X-linked 55;
  • Gene: [0X^/MRX56] mental retardation, X-linked 56;
  • Gene: [0X^/MRX57] mental retardation, X-linked 57;
  • Gene: [0X^/MRX58] mental retardation, X-linked 58;
  • Gene: [0X^/MRX59] mental retardation, X-linked 59;
  • Gene: [0X^/MRX61] mental retardation, X-linked 61;
  • Gene: [0X^/MRX62] mental retardation, X-linked 62;
  • Gene: [0X^/MRX63] mental retardation, X-linked 63;
  • Gene: [0X^/MRX65] mental retardation, X-linked 65;
  • Gene: [0X^/MRX7] mental retardation, X-linked 7;
  • Gene: [0X^/MRXS7] mental retardation, X-linked, syndromic 7;
  • Gene: [0X^/MSD] microcephaly with spastic diplegia (Paine syndrome);
  • Gene: [0X^/MYP1] myopia 1 (X-linked, Bornholm eye disease included); [BED ]
  • Gene: [0X^/NAC] neurocanthocytosis; [NA ]
  • Gene: [0X^/NSX] N syndrome (mental retardation, malformations, chromosome breakage);
  • Gene: [0X^/NYS1] nystagmus 1, congenital; [NYS ]
  • Gene: [0X^/ODT1] oligodontia 1;
  • Gene: [0X^/OFD1] orofaciodigital syndrome 1;
  • Gene: [0X^/OPD2] otopalatodigital syndrome 2 (cranioorodigital syndrome); [OPD ]
  • Gene: [0X^/OPEM] ophthalmoplegia, external, with myopia;
  • Gene: [0X^/PCNAP] cyclin pseudogene; proliferating cell nuclear antigen, pseudogene;
  • Gene: [0X^/PLS3] plastin 3 (T isoform);
  • Gene: [0X^/PSBG1L2] beta-1-glycoprotein, pregnancy specific like 2; [B1G2 SP2 ]
  • Gene: [0X^/PSF2] protein spot in 2-D gels (MM 27 kD);
  • Gene: [0X^/PSF3] protein spot in 2-D gels (MM 37 kD);
  • Gene: [0X^/PSF4] protein spot in 2-D gels (MM 40 kD);
  • Gene: [0X^/PYHG12] protein spot in 2-D gels (MM 55 kD);
  • Gene: [0X^/PYHG17] protein spot in 2-D gels (MM 32 kD);
  • Gene: [0X^/PYHG4] protein spot in 2-D gels (MM 104 kD);
  • Gene: [0X^/RENS1] Renpenning syndrome 1; mental retardation, X-linked, syndromic 8; [MRXS8 ]
  • Gene: [0X^/RENS2] Renpenning syndrome 2 (Renpenning-like syndrome); mental retardation, X-linked, syndromic 9; [MRXS9 ]
  • Gene: [0X^/RP16] retinitis pigmentosa 16 (X-linked recessive);
  • Gene: [0X^/RTT] Rett syndrome (autism/dementia/ataxia/loss of purposeful hand use);
  • Gene: [0X^/S12] surface antigen S12 (X-linked 3);
  • Gene: [0X^/SEN3] senescence (cellular)-related 3;
  • Gene: [0X^/SHS] Sutherland-Haan syndrome; mental retardation, X-linked, syndromic 3 (with spastic diplegia); [MRXS3 ]
  • Gene: [0X^/SUP45L4] sup45 (yeast omnipotent suppressor 45) homolog-like 4;
  • Gene: [0X^/TDD] testicular 17,20-desmolase, deficiency of?; pseudohermaphroditism, male, due to testicular desmolase deficiency;
  • Gene: [0X^/TMSL7] thymosin-like 7;
  • Gene: [0X^/WTS] Wilson-Turner syndrome; mental retardation, X-linked, syndromic 6 (ginecomastia/obesity); [MRXS6 ]
  • Gene: [0X^/XLRL] X-linked B cell surface antigen (mouse)-like 1;
  • Gene: [0X^/XM] XM antigen;
  • Gene: [0Yp1/SMCY] selected mouse cDNA on the Y;
  • Gene: [0Yp1/TSPY] testis-specific protein, Y-linked;
  • Gene: [0Yp1/XE7Y] pseudoautosomal gene XE7, Y-linked;
  • Gene: [0Yp11/HYA] histocompatibility Y antigen, Y-linked; [HY HYS ]
  • Gene: [0Yp11/MIC2Y] antigen MIC2, Y-linked (monoclonal antibodies 12E7, F21, O13); [MIC2 ]
  • Gene: [0Yp112/AMELY] amelogenin, Y-linked; [AMGY AMGL ]
  • Gene: [0Yp112/PRKY] protein kinase, Y-linked;
  • Gene: [0Yp112/TDF] testis-determining factor, Y-linked; histocompatibility Y antigen, inductor Y-linked; gonadal dysgenesis, XY female type (Swyer syndrome); [HYAI GDXYF ]
  • Gene: [0Yp113/ANT3Y] adenine nucleotide translocator 3 (liver), Y-linked;
  • Gene: [0Yp113/ASMTY] acetylserotonin N-methyltransferase, Y-linked;
  • Gene: [0Yp113/CSF2RAY] colony stimulating factor 2 (granulocyte-macrophage) receptor, alpha, low-affinity, Y-linked; granulocyte-macrophage factor CSF2 receptor, alpha, Y-linked (antigen CDW116); [CSF2RA CSF2R ]
  • Gene: [0Yp113/IL3RAY] interleukin 3 receptor, alpha, Y-linked (low affinity; antigen CD123); [IL3RA ]
  • Gene: [0Yp113/PABY] pseudoautosomal boundary region, Y-linked;
  • Gene: [0Yp113/RPS4Y] ribosomal protein S4, Y-linked;
  • Gene: [0Yp113/SHOXY] short stature homeobox, Y-linked; pseudoautosomal homeobox-containing osteogenic gene, Y-linked; short stature, idiopathic; [PHOG SHOX ]
  • Gene: [0Yp113/SRY] sex determining region Y; gonadal dysgenesis, XY female type; sex reversal with partial ovarian function;
  • Gene: [0Yp113/XGRY] XG blood group regulator, Y-linked; expression of XG and MIC2 on erythrocytes, Y-linked; antigen XG, expression on erythrocytes, Y-linked; [XGR ]
  • Gene: [0Yp113/ZNFY] zinc finger protein, Y-linked; [ZFY ]
  • Gene: [0Yq1/TB4Y] thymosin, beta 4, Y-linked;
  • Gene: [0Yq11/ACTGP2] actin, gamma pseudogene 2; [ACTL2 ]
  • Gene: [0Yq11/ARSC1P] arylsulfatase C, S isozyme, Y-linked pseudogene; steroid sulfatase, microsomal, Y-linked pseudogene; [STSP ]
  • Gene: [0Yq11/ARSDP] arylsulfatase D, Y-linked pseudogene;
  • Gene: [0Yq11/ARSEP] arylsulfatase E, Y-linked pseudogene;
  • Gene: [0Yq11/ARSFP] arylsulfatase F, Y-linked pseudogene;
  • Gene: [0Yq11/AZF1] azoospermia factor 1; azoospermia factor (Sertoli-cell-only syndrome);
  • Gene: [0Yq11/AZF2] azoospermia factor 2;
  • Gene: [0Yq11/AZF3] azoospermia factor 3;
  • Gene: [0Yq11/GCY] growth control, Y chromosome influenced (stature; tooth size); [STA TS TSY ]
  • Gene: [0Yq11/KALP] Kallmann syndrome sequence pseudogene; adhesion molecule-like, Y-linked pseudogene; [ADMLY ]
  • Gene: [0Yq11/RBM2] RNA binding motif protein 2; [YRRM2 ]
  • Gene: [0Yq112/DFFRY] ubiquitin carboxyl-terminal hydrolase faf-Y; Drosophila fat facets related, Y-linked;
  • Gene: [0Yq1121/XGPY] XG pseudogene (Y-linked);
  • Gene: [0Yq1123/RBM1] RNA binding motif protein 1; [YRRM1 ]
  • Gene: [0Yq12/DAZ] deleted in azoospermia;
  • Gene: [0Yq12/DYZ1] classical satellite, based on CCATT; 3.4 kb repeat;
  • Gene: [0Yq12/DYZ2] classical satellite; 2.1 kb repeat;
  • Gene: [0Yq12/FRAYA] fragile site Yq12, unclassified type, commom;
  • Gene: [0Yq12/IL9RY] interleukin 9 receptor, Y-linked homolog; [IL9R ]
  • Gene: [0Y^/ASSP6] argininosuccinate synthetase pseudogene 6; [ASSPY ]
  • Gene: [0Y^/ERVNP2] endogenous retroviral sequences NP2; [RVNP2 ]
  • Gene: [0Y^/UBE1Y] ubiquitin-activating enzyme E1, Y-linked;
  • Gene: [0Y^/YG] MIC2 red cell polymorphism control by the Y-born locus, YG;
  • Gene: [10p1/CALML3] calmodulin-like 3;
  • Gene: [10p1/CHDR] chlordecone reductase (EC:1.1.1.225); 3-alpha-hydroxysteroid dehydrogenase (EC:1.1.1.50);
  • Gene: [10p1/CREM] cAMP responsive element modulator;
  • Gene: [10p1/DDH2] dihydrodiol dehydrogenase 2; trans-1,2-dihydrobenzene-1,2-diol dehydrogenase; chlordecone reductase-like 1;
  • Gene: [10p1/DNMT2] DNA (cytosine-5-)-methyltransferase 2; DNA methyltransferase 2;
  • Gene: [10p1/GLC1E] glaucoma 1, open angle, E (adult-onset);
  • Gene: [10p1/IL15RA] interleukin 15 receptor, alpha;
  • Gene: [10p1/IL2RA] interleukin 2 receptor, alpha (high affinity; Tac antigen); antigen Tac (antigen CD25; p55; interleukin 2 receptor alpha); [TCGFR TAC ]
  • Gene: [10p1/PFKFB3] 6-phosphofructo-2-kinase 3 (EC:2.7.1.105); fructose-2,6-biphosphatase 3 (EC:3.1.3.46);
  • Gene: [10p1/PHYH] phytanoyl-CoA hydroxylase; Refsum disease (MIM:266500);
  • Gene: [10p1/SCIDA] severe combined immunodeficiency, type a (Athabascan); [A-SCID ]
  • Gene: [10p11/TPL2] tumor progression locus 2;
  • Gene: [10p112/EWST] Ewing sarcoma transformant; [ESTF ]
  • Gene: [10p112/GKP5] glycerol kinase pseudogene 5;
  • Gene: [10p112/GLUDP5] glutamate dehydrogenase pseudogene 5;
  • Gene: [10p112/ITGB1] integrin, beta 1 (antigen CD29 includes MDF2, MSK12); fibronectin receptor, beta polypeptide (antigen CD29 includes MDF2, MSK12); very late activation protein-4 receptor, beta-4 subunit (antigen CD29); [FNRB CD29 ]
  • Gene: [10p112/TCF8] transcription factor 8; interleukin 2 inhibitor; zinc finger protein Nil-2-a; [Nil-2-a ]
  • Gene: [10p112/ZNF11A] zinc finger protein 11a (KOX 2); [ZNF11 KOX2 ]
  • Gene: [10p112/ZNF25] zinc finger protein 25 (KOX 19); [KOX19 ]
  • Gene: [10p112/ZNF33A] zinc finger protein 33a (KOX 31); [KOX31 ZNF33 ]
  • Gene: [10p112/ZNF37A] zinc finger protein 37a (KOX 21); [KOX21 ZNF37 ]
  • Gene: [10p1123/GAD2] glutamate decarboxylase 2 (pancreatic islets and brain, 65kD);
  • Gene: [10p12/CACNB2] calcium channel, voltage-dependent, beta 2 subunit; calcium channel, L type, beta 2 polypeptide; myasthenic (Lambert-Eaton) syndrome antigen B; Lambert-Eaton myasthenic syndrome; [CACNLB2 MYSB ]
  • Gene: [10p12/MLLT8] myeloid/lymphoid or mixed-lineage leukemia (trithorax (Drosophila) homolog); translocated to, 8; [AF10 ]
  • Gene: [10p121/CUBN] cubilin (intrinsic factor-cobalamin receptor); [IFCR ]
  • Gene: [10p121/MGA1] megaloblastic anemia 1 (enterocyte cobalamin malabsorption); Imerslund-Grasbeck syndrome; [IGS ]
  • Gene: [10p13/BMI1] murine leukemia viral (bmi-1) oncogene homolog;
  • Gene: [10p13/MRC1] mannose receptor, C type 1;
  • Gene: [10p13/VIM] vimentin;
  • Gene: [10p14/DDH1] dihydrodiol dehydrogenase 1; trans-1,2-dihydrobenzene-1,2-diol dehydrogenase, high affinity bile acid binding; chlordecone reductase-like 2; chlordecone reductase-like 3;
  • Gene: [10p15/COPEB] core promoter element binding protein; B-cell derived 1; [CPBP BCD1 ]
  • Gene: [10p15/GATA3] GATA-binding protein 3 (T-cell specific transcription factor);
  • Gene: [10p15/GDI2] GDP dissociation inhibitor 2; rab GDP-dissociation inhibitor, beta; [RABGDIB ]
  • Gene: [10p15/IL9RP2] interleukin 9 receptor pseudogene 2;
  • Gene: [10p15/ITIH2] inter-alpha-trypsin inhibitor, H2 polypeptide (of protein HC);
  • Gene: [10p15/PFKP] phosphofructokinase, platelet type; phosphofructokinase, red cell type (MIM:171850);
  • Gene: [10p15/PRKCQ] protein kinase C, theta polypeptide;
  • Gene: [10q/ADK] adenosine kinase;
  • Gene: [10q/ALDOAP2] aldolase A, fructose-bisphosphate pseudogene 2;
  • Gene: [10q/CTSLL1] cathepsin L-like 1;
  • Gene: [10q/DHFRL1] dihydrofolate reductase, like 1;
  • Gene: [10q/GPR7] G protein-coupled receptor 7;
  • Gene: [10q/PNIA1] protein spot in 2-D gels (40kD; pI 5.25);
  • Gene: [10q/PNIA3] protein spot in 2-D gels (30kD; pI 5.6);
  • Gene: [10q/PPIP3] peptidylprolyl cis-trans-isomerase (cyclophilin) pseudogene 3;
  • Gene: [10q/PP] pyrophosphatase (inorganic);
  • Gene: [10q/TACR2] tachykinin receptor 2 (substance K receptor, neurokinin 2 receptor); [NK2R ]
  • Gene: [10q/USH1D] Usher syndrome 1D (autosomal recessive, severe);
  • Gene: [10q11/ERCC6] excision repair cross-complementing rodent repair deficiency, complementation group 6; Cockayne syndrome B protein; Cockayne syndrome 2 (late onset form B); [CKN2 CSB ]
  • Gene: [10q11/RHEB1] Ras homolog enriched in brain 1; [RHEB ]
  • Gene: [10q112/ALOX5] arachidonate 5-lipoxygenase (leukotrien A4 synthase); arachidonate 5-lipoxygenase, variable expression of;
  • Gene: [10q112/ANX8] annexin VIII; placental anticoagulant protein IV (vascular anticoagulant, beta);
  • Gene: [10q112/CHAT] choline acetyltransferase;
  • Gene: [10q112/DUSP8P] dual specificity phosphatase 8 pseudogene;
  • Gene: [10q112/FRA10G] fragile site 10q11.2, aphidicolin type, common;
  • Gene: [10q112/GLUDP2] glutamate dehydrogenase pseudogene 2;
  • Gene: [10q112/HNRPF] heterogeneous nuclear ribonucleoprotein F; RNP particle, heterogeneous nuclear, F protein;
  • Gene: [10q112/MBL2] mannose-binding lectin (protein C) 2, soluble (32kD; opsonic defect); recurrent infections, predisposition?; [MBL MBP ]
  • Gene: [10q112/MSMB] microseminoprotein, beta (seminal plasma beta-inhibin); prostate secreted seminal plasma protein (PSP-94); [MSPB PSP-94 ]
  • Gene: [10q112/NPY4R] neuropeptide Y receptor Y4; pancreatic polypeptide receptor 1; [PPYR1 PP1 Y4 ]
  • Gene: [10q112/PRKG1] protein kinase, cGMP-dependent, type I;
  • Gene: [10q112/RBPI1] retinol-binding protein 3, interstitial; [RBP3 IRBP RBP ]
  • Gene: [10q112/RET] proto-oncogene tyrosine-protein kinase receptor ret; multiple endocrine neoplasia, type IIA (MEN2A; MIM:171400); amyloid-producing familial medullary thyroid carcinoma (MIM:171400); pheochromocytoma and familial amyloid-p
  • Gene: [10q112/SDF1] stromal cell-derived factor 1; [SDF1A SDF1B ]
  • Gene: [10q112/SLC18A3] solute carrier family 18 (vesicular acetylcholine), member 3; [VACHT ]
  • Gene: [10q112/TST1] transforming sequence, thyroid 1 (protein H4); PTC1 chimeric oncogene; thyroid carcinoma, papillary (MIM:188550); [PACT PTC ]
  • Gene: [10q112/ZNF11B] zinc finger protein 11b (KOX 2); [KOX2 ]
  • Gene: [10q112/ZNF22] zinc finger protein 22 (KOX 15); [KOX15 ]
  • Gene: [10q112/ZNF33B] zinc finger protein 33b (KOX 31); [KOX31 ]
  • Gene: [10q112/ZNF37B] zinc finger protein 37b (KOX 21); [KOX21 ]
  • Gene: [10q2/ACADSB] acyl-Coenzyme A dehydrogenase, short/branched chain;
  • Gene: [10q2/ACTA2] actin, alpha 2, smooth muscle, aortic;
  • Gene: [10q2/ADORA2L1] adenosine A2 receptor-like 1; [ADORA2L ]
  • Gene: [10q2/ANX11] annexin XI (56kD autoantigen);
  • Gene: [10q2/ANX2P3] annexin II (lipocortin II) pseudogene 3; [ANX2L3 LPC2C ]
  • Gene: [10q2/CD39] ATP diphosphohydrolase (vascular); antigen CD39;
  • Gene: [10q2/CMD1C] cardiomyopathy, dilated 1C (autosomal dominant);
  • Gene: [10q2/CTSLL3] cathepsin L-like 3;
  • Gene: [10q2/DFNB12] deafness, autosomal recessive 12;
  • Gene: [10q2/DMBT1] deleted in malignant brain tumors 1; malignant brain tumors, locus 1 (medulloblastoma; glioblastoma multiforme);
  • Gene: [10q2/DNA2L] DNA2 (DNA replication helicase, yeast, homolog)-like;
  • Gene: [10q2/DNTT] deoxynucleotidyltransferase, terminal;
  • Gene: [10q2/EIF4EBP2] eukaryotic translation initiation factor 4E binding protein 2;
  • Gene: [10q2/EPT] epilepsy, partial;
  • Gene: [10q2/FGF8] fibroblast growth factor 8 (androgen-induced);
  • Gene: [10q2/FGFR2] fibroblast growth factor receptor 2 (bacteria-expressed kinase); keratinocyte growth factor receptor; protein tyrosine kinase FGFR-like 2 (BEK-related); craniofacial dysostosis 1 (Crouzon syndrome; MIM:123500); Pfeiffer s
  • Gene: [10q2/FRA10A] fragile site 10q23.3, folic acid type, rare;
  • Gene: [10q2/GDA] Graves' disease autoantigen; [D10S105E ]
  • Gene: [10q2/GPR10] G protein-coupled receptor 10;
  • Gene: [10q2/GPRK5] G protein-coupled receptor kinase 5;
  • Gene: [10q2/HABP2] hyaluronan-binding protein 2; [HABP PHBP ]
  • Gene: [10q2/HMX2] homeo box (H6 family) 2; [H6L ]
  • Gene: [10q2/HTR7] 5-hydroxytryptamine (serotonin) receptor 7 (adenylate cyclase-coupled);
  • Gene: [10q2/IDE] insulin-degrading enzyme (insulinase);
  • Gene: [10q2/IFNI54] interferon, alpha-inducible protein 54 (clone IFI-54K); [G10P2 IFI54 ]
  • Gene: [10q2/IFNI56] interferon, alpha-inducible protein 56 (clone IFI-56K); [IFI56 IFNAI1 ]
  • Gene: [10q2/IKBKA] inhibitor of kappa light polypeptide gene enhancer in B-cells, kinase alpha; conserved helix-loop-helix ubiquitous kinase;
  • Gene: [10q2/IOSCA] infantile onset spinocerebellar ataxia (autosomal recessive); spinocerebellar ataxia 8 (infantile, with sensory neuropathy); [SCA8 ]
  • Gene: [10q2/MKI67] antigen Ki-67 (nuclear; proliferation-related); antigen identified by monoclonal antibody Ki-67; [KIA Ki67 ]
  • Gene: [10q2/NRAP] nebulin-related anchoring protein;
  • Gene: [10q2/P4HA] prolyl 4-hydroxylase, alpha subunit (64 kD); procollagen-proline, 2-oxoglutarate 4-dioxygenase, alpha;
  • Gene: [10q2/PAX2] paired box homeotic gene 2; optic nerve coloboma with renal disease (ONCR; MIM:120330); [ONCR ]
  • Gene: [10q2/PEO1] progressive external ophthalmoplegia, type 1; [PEO ]
  • Gene: [10q2/PPP1R5] protein phosphatase 1, regulatory subunit 5 (inhibitor);
  • Gene: [10q2/PPP3CB] protein phosphatase 3, catalytic subunit, beta isoform; calcineurin A beta;
  • Gene: [10q2/PRSS11] protease, serine, 11 (IGF binding);
  • Gene: [10q2/SFTPA1] surfactant, pulmonary-associated protein A1 (SP-A1; 35kD); [SFTP1 PSPA ]
  • Gene: [10q2/SFTPA2] surfactant, pulmonary-associated protein A2 (SP-A2);
  • Gene: [10q2/SFTPD] surfactant, pulmonary-associated protein D (SP-D); [SFTP4 PSPD ]
  • Gene: [10q2/SHFM3] split hand/foot malformation (ectrodactyly) type 3;
  • Gene: [10q2/TAF2D] TATA box binding protein (TBP)-associated factor, RNA polymerase II, D, 100kD; [TAFII100 ]
  • Gene: [10q2/UFS] urofacial syndrome (Ochoa syndrome);
  • Gene: [10q2/UROS] uroporphyrinogen-III synthase (UPS3-deficiency, Gunther type); porphyria, congenital erythropoetic (Gunther disease);
  • Gene: [10q2/VCL] vinculin (alpha-actinin and talin binding protein);
  • Gene: [10q2/ZNF32] zinc finger protein 32 (KOX 30); [KOX30 ]
  • Gene: [10q21/ANK3] ankyrin 3, node of Ranvier (ankyrin G);
  • Gene: [10q21/ANX7] annexin VII (synexin);
  • Gene: [10q21/FRA10C] fragile site 10q21, BrdU type, common;
  • Gene: [10q21/TFAM] transcription factor A, mitochondrial; transcription factor 6 (mitochondrial transcription factor A); [TCF6 TCF6L2 ]
  • Gene: [10q211/CDC2] cell division cycle 2, G1 to S and G2 to M; protein kinase p34/CDC2;
  • Gene: [10q211/EGR2] early growth response 2 (transcription factor Krox20-like); zinc-finger protein EGR2 (early growth response 2; Krox20-like); [KROX20 ]
  • Gene: [10q22/CAMK2G] calcium/calmodulin-dependent protein kinase (CaM kinase) 2 gamma;
  • Gene: [10q22/COL13A1] collagen, type XIII, alpha 1;
  • Gene: [10q22/CTSLL2] cathepsin L-like 2;
  • Gene: [10q22/HK1] hexokinase 1 (brain); hemolytic anemia due to hexokinase deficiency (MIM:235700);
  • Gene: [10q22/HNRPH3] heterogeneous nuclear ribonucleoprotein H3 (H'); RNP particle, heterogeneous nuclear, H3 protein;
  • Gene: [10q22/NDST2] N-deacetylase/N-sulfotransferase 2; heparan sulfate-N-deacetylase/N-sulfotransferase 2;
  • Gene: [10q22/PCBD] pterin-4-alpha-carbinolamine dehydratase; dimerization cofactor of hepatocyte nuclear factor 1 alpha; 6-pyruvoyl-tetrahydropterin synthase/dimerization cofactor; hyperphenylalaninemia, mild (MIM:264070);
  • Gene: [10q22/PRF1] perforin 1 (lymphocyte pore forming protein); [PFP ]
  • Gene: [10q22/SAMS1] S-adenosylmethionine synthetase 1, alpha and beta (liver-specific); hypermethioninemia (methionine adenosyltransferase deficiency);
  • Gene: [10q221/FRA10D] fragile site 10q22.1, aphidicolin type, common;
  • Gene: [10q221/GLUDP3] glutamate dehydrogenase pseudogene 3;
  • Gene: [10q221/PRG1] proteoglycan 1, secretory granule; [PRG ]
  • Gene: [10q221/PSAP] prosaposin (saposin A, saposin B, saposin C, saposin D); sphingolipid activator protein 1 (SAP1; saposin B); sphingolipid activator protein 2 (SAP2; saposin C); metachromatic leukodystrophy (deficiency of SAP1 (saposin B
  • Gene: [10q23/HPS] Hermansky-Pudlak syndrome;
  • Gene: [10q23/LIPA] lipase A, lysosomal acid (3.1.1.3); cholesterol esterase (EC:3.1.1.13); Wolman disease (lysosomal acid cholesteryl ester hydrolase deficiency);
  • Gene: [10q23/RGR] retinal G protein coupled receptor;
  • Gene: [10q23/RPS24] ribosomal protein S24;
  • Gene: [10q23/SNCG] synuclein, gamma (persyn); breast cancer-specific protein 1; [BCSG1 PRSN ]
  • Gene: [10q233/EIF5AP1] eukaryotic translation initiation factor 5A pseudogene 1;
  • Gene: [10q233/GLUD1] glutamate dehydrogenase 1, liver; hyperinsulinism-hyperammonemia syndrome;
  • Gene: [10q233/PTEN] phosphatase and tensin homolog; mutated in multiple advanced cancers 1; protein-tyrosine phosphatase PTEN; Bannayan-Zonana syndrome (MIM:153480); Bannayan-Riley-Ruvalcaba syndrome (MIM:153480); multiple hamartoma (Cowden
  • Gene: [10q24/ADDL] adducin-like protein (70);
  • Gene: [10q24/BUB3] mitotic checkpoint component BUB3 (BUB1 ligand);
  • Gene: [10q24/CDB2] corneal dystrophy of Bowman's layer type II (Thiel-Behnke); [CDTB ]
  • Gene: [10q24/CMOAT] canalicular multispecific organic anion transporter; multiple drug resistance-associated protein 2; hyperbilirubinemia II (Dubin-Johnson syndrome; MIM:237500); [ABC DJS MRP2 ]
  • Gene: [10q24/HOX11] homeo box 11, homologous to Drosophila Notch; protooncogene TCL3; T cell lymphoma 3 associated breakpoint;
  • Gene: [10q24/HPV6AI1] human papillomavirus (type 6a) integration site 1;
  • Gene: [10q24/NFKB2] nuclear factor of kappa light chain gene enhancer in B-cells 2 (p49/p100); transcription factor kappa-B, subunit 2 (p49/p100); oncogene LYT-10; v-rel avian reticuloendotheliosis viral oncogene homolog B; [LYT10 RELB ]
  • Gene: [10q24/PDE6C] phosphodiesterase 6C, cGMP-specific, cone, alpha prime;
  • Gene: [10q24/PLGAU] plasminogen activator, urokinase;
  • Gene: [10q24/PSD] pleckstrin and Sec7 domain protein;
  • Gene: [10q24/WNT8B] wingless-type MMTV integration site 8B, human homolog;
  • Gene: [10q241/APT1] apoptosis (APO-1) antigen 1 (CD95); [APT APO1 FAS ]
  • Gene: [10q241/CYP2C10] cytochrome P450, subfamily IIC (mephenytoin 4-hydroxylase), polypeptide 10;
  • Gene: [10q241/CYP2C18] cytochrome P450, subfamily IIC (mephenytoin 4-hydroxylase), polypeptide 18;
  • Gene: [10q241/CYP2C19] cytochrome P450, subfamily IIC (mephenytoin 4-hydroxylase), polypeptide 19; mephenytoin 4-hydroxylase C19 (cytochrome P450 IIC19) defect (mephenytoin 4-hydroxylase poor metabolizer);
  • Gene: [10q241/CYP2C8] cytochrome P450, subfamily IIC (mephenytoin 4-hydroxylase), polypeptide 8;
  • Gene: [10q241/CYP2C9] cytochrome P450, subfamily IIC (mephenytoin 4-hydroxylase), polypeptide 9; mephenytoin 4-hydroxylase C9 (cytochrome P450 IIC9) defect (tolbutamide poor metabolizer);
  • Gene: [10q241/KNSL1] kinesin-like 1; kinesin-related motor protein EG5; thyroid hormone receptor interactor 5; [EG5 TRIP5 ]
  • Gene: [10q241/RBPI2] retinol-binding protein 4, plasma; [RBP4 PRBP ]
  • Gene: [10q243/COL17A1] collagen, type XVII, alpha 1; bullous pemphigoid antigen 2 (180kD); epidermolysis bullosa, generalized atrophic benign (MIM:226650); [BPAG2 BP180 ]
  • Gene: [10q243/CYP17] cytochrome P450, subfamily XVII (steroid 17-alpha-hydroxylase); adrenal hyperplasia V (17-alpha-hydroxylase deficiency);
  • Gene: [10q243/CYP2E1] cytochrome P450, subfamily IIE (ethanol-inducible), polypeptide 1;
  • Gene: [10q243/PYCS] pyrroline-5-carboxylate synthetase, delta 1-; glutamate 5-kinase (gamma-glutamyl kinase; GK; EC:2.7.2.11); glutamate-5-semialdehyde dehydrogenase (glutamate gamma-semialdehyde synthetase; GSAS; EC:1.2.1.41);
  • Gene: [10q25/ADRA2A] adrenergic, alpha-2A-, receptor (platelet); [ADRA2 ADRA2R ]
  • Gene: [10q25/ADRB1] adrenergic, beta-1-, receptor; [ADRB1R B1AR ]
  • Gene: [10q25/CASP7] caspase 7, apoptosis-related cysteine protease; craniofacial dysostosis 1? (Crouzon syndrome; MIM:123500);
  • Gene: [10q25/DUSP5] dual specificity phosphatase 5 (EC:3.1.3.48 and EC:3.1.3.16);
  • Gene: [10q25/MXI1] MAX-interacting protein 1; prostate cancer 1 (MIM:176807); [PRCA1 ]
  • Gene: [10q25/PITX3] paired-like homeodomain transcription factor 3; pituitary homeo box 3; anterior segment mesenchymal dysgenesis (MIM:107250); [PTX3 ]
  • Gene: [10q25/SLC18A2] solute carrier family 18 (vesicular monoamine), member 2 (synaptic vesicle); [VMAT2 SVMT ]
  • Gene: [10q252/FRA10B] fragile site 10q25.2, BrdU type, rare;
  • Gene: [10q252/FRA10E] fragile site 10q25.2, aphidicolin type, common;
  • Gene: [10q253/GOT1] glutamic-oxaloacetic transaminase 1, soluble;
  • Gene: [10q253/PGAM1] phosphoglycerate mutase 1 (A; brain);
  • Gene: [10q26/DEC] tumor suppressor DEC (putative); deleted in endometrial carcinoma; endometrial carcinoma;
  • Gene: [10q26/DOCK1] dedicator of cyto-kinesis 1; downstream of CRK-binding protein, 180 kD; [DOCK180 ]
  • Gene: [10q26/ECHS1] enoyl-CoA hydratase, short chain, 1, mitochondrial;
  • Gene: [10q26/GFRA1] GDNF family receptor alpha 1; glial cell line derived neurotrophic factor receptor alpha; TGF-beta related neurotrophic factor 2; [GDNFRA TRNR1 ]
  • Gene: [10q26/MGMT] methylguanine-DNA methyltransferase;
  • Gene: [10q26/OATL3] ornithine aminotransferase-like 3;
  • Gene: [10q26/OAT] ornithine aminotransferase; gyrate atrophy of choroid/retina (OAT deficiency);
  • Gene: [10q26/PTPRE] protein tyrosine phosphatase, receptor type, epsilon polypeptide;
  • Gene: [10q261/EMX2] homeobox protein EMX2; empty spiracles (Drosophila) homolog 2;
  • Gene: [10q261/FRA10F] fragile site 10q26.1, aphidicolin type, common;
  • Gene: [10q261/PNLIP] pancreatic lipase (56kD); diarrhea, congenital, due to pancreatic lipase deficiency;
  • Gene: [10q263/ADAM8] a disintegrin and metalloprotease domain 8; cell surface antigen MS2 (CD156 antigen);
  • Gene: [10q263/INPP5A] inositol polyphosphate-5-phosphatase, type I, 43kD;
  • Gene: [10q263/MLTN] meltrin-alpha, mouse, homolog of; a disintegrin and metalloprotease domain 12;
  • Gene: [10^/ATP5CL1] ATP synthase, H+ transporting, mitochondrial F1 complex, gamma polypeptide-like 1;
  • Gene: [10^/CTSLL] cathepsin L-like;
  • Gene: [10^/EIF3S10] eukaryotic translation initiation factor 3, subunit 10 (theta, 170kD); eukaryotic translation initiation factor 3A (p180, p170); cytoplasmic protein p167; centrosomin A, mouse, homolog of; [KIAA0139 ]
  • Gene: [10^/FUSE] polykaryocytosis promoter;
  • Gene: [10^/HEP10] hepatic protein 10; [HP10 ]
  • Gene: [10^/IDDM10] insulin-dependent diabetes mellitus 10;
  • Gene: [10^/KCNMA1] potassium large conductance calcium-activated channel, subfamily M, alpha member 1; slowpoke (Drosophila) homolog, alpha; [SLOA ]
  • Gene: [10^/LDHAL5] lactate dehydrogenase A-like 5;
  • Gene: [10^/LMNACL2] lamin A/C-like 2; [LMNL2 ]
  • Gene: [10^/M130] external membrane protein (MM 130 kD);
  • Gene: [10^/NET1] neuro epithelioma transforming gene 1; guanine nucleotide regulatory protein NET1;
  • Gene: [10^/NEU] glycoprotein neuraminidase (sialidosis); sialidosis (neuraminidase deficiency);
  • Gene: [10^/PRHX] homeobox protein PRH; proline-rich homeodomain-containing transcription factor;
  • Gene: [10^/PRKM8] protein kinase, mitogen-activated 8 (MAP kinase); stress-activated protein kinase 1; c-jun N-terminal kinase 1;
  • Gene: [10^/PROA] proline'-' auxotroph, complementation of;
  • Gene: [10^/PYGBL] phosphorylase, glycogen; brain-like;
  • Gene: [10^/PYHG18] protein spot in 2-D gels (MM 31 kD);
  • Gene: [10^/PYHG1] protein spot in 2-D gels (MM 218 kD);
  • Gene: [10^/RSU1] Ras suppressor protein 1;
  • Gene: [10^/SFTPAP1] surfactant, pulmonary-associated protein A pseudogene 1; [SFTPP1 ]
  • Gene: [10^/SLC9A3P] solute carrier family 9 (sodium/hydrogen exchanger), isoform 3 pseudogene;
  • Gene: [10^/ST12] suppression of tumorigenicity 12 (prostate); prostate adenocarcinoma 1; [PAC1 ]
  • Gene: [10^/TAKUL3] thyroid autoantigen-like 3; [TSHRL3 ]
  • Gene: [10^/USH1F] Usher syndrome 1F (autosomal recessive, severe; retinitis/deafness);
  • Gene: [11p1/ALDRL3] aldehyde reductase (aldose reductase)-like 3;
  • Gene: [11p1/AMPD3] adenosine monophosphate deaminase 3 (isoform E);
  • Gene: [11p1/CALCB] calcitonin gene related peptide beta;
  • Gene: [11p1/CHRM4] cholinergic receptor, muscarinic 4;
  • Gene: [11p1/DDB2] damage-specific DNA binding protein 2 (48kD);
  • Gene: [11p1/DFNB18] deafness, autosomal recessive 18;
  • Gene: [11p1/ELF5] E74-like factor 5 (ets domain transcription factor);
  • Gene: [11p1/EXT2] exostosin 2; exostoses (multiple) 2;
  • Gene: [11p1/GAS2] growth arrest-specific 2;
  • Gene: [11p1/GTF2H1] general transcription factor IIH, polypeptide 1 (62kD subunit);
  • Gene: [11p1/LDHCL] lactate dehydrogenase C-like sequences (multiple);
  • Gene: [11p1/LHX1] LIM homeobox protein 1;
  • Gene: [11p1/MER1] antigen MER1 (MIC1; monoclonal antibodies W6/34, 5C1); lethal antigen 1 (A1; AL-A1; SA11-1; A1; AL-A1); [MIC1 S1 ]
  • Gene: [11p1/MSK14] antigen MSK14 (monoclonal antibody JF23);
  • Gene: [11p1/MSK24] antigen MSK24 (monoclonal antibody NP13);
  • Gene: [11p1/MSK35] antigen MSK35 (monoclonal antibody SR27);
  • Gene: [11p1/PIGCP1] phosphatidylinositol glycan, class C, pseudogene 1;
  • Gene: [11p1/RDXP1] radixin pseudogene 1;
  • Gene: [11p1/RPS13] ribosomal protein S13;
  • Gene: [11p1/RPS17] ribosomal protein S17;
  • Gene: [11p1/SLC1A2] solute carrier family 1 (glial high affinity glutamate transporter), member 2; glutamate transporter 1; [EAAT2 GLT1 ]
  • Gene: [11p1/SPI1] spleen focus forming virus (SFFV) proviral integration oncogene spi1; [SFFVpi ]
  • Gene: [11p1/ST2] suppression of tumorigenicity 2;
  • Gene: [11p1/TRPH] tryptophan hydroxylase (tryptophan 5-monooxygenase);
  • Gene: [11p11/ACP2] acid phosphatase 2, lysosomal;
  • Gene: [11p11/RAPSN] receptor-associated protein of the synapse, 43kD (rapsyn);
  • Gene: [11p112/DGKZ] diacylglycerol kinase, zeta (104kD);
  • Gene: [11p112/KAI1] kangai 1 (suppression of tumorigenicity 6, prostate); suppression of tumorigenicity 6 (prostate); CD82 antigen (R2 leukocyte antigen, detected by monoclonal antibody IA4); [ST6 CD82 ]
  • Gene: [11p112/MDK] midkine (neurite growth-promoting factor 2); [NEGF2 ]
  • Gene: [11p112/MYBPC3] myosin-binding protein C, cardiac; cardiomyopathy, hypertrophic 4 (MIM:115197); [MYBP-C CMH4 ]
  • Gene: [11p112/PHBP2] prohibitin pseudogene 2;
  • Gene: [11p112/PSMC3] proteasome (prosome, macropain) 26S subunit, ATPase, 3 (homolog of yeast YTA1); 26S protease regulatory subunit TBP1 (TAT-binding protein 1); [TBP1 ]
  • Gene: [11p112/TYRL] tyrosinase-like;
  • Gene: [11p13/BDNF] brain-derived neurotrophic factor;
  • Gene: [11p13/BP239F] fetal brain protein 239; [239FB ]
  • Gene: [11p13/CAT] catalase (CAT deficiency; acatalasia); acatalasia (acatalasemia);
  • Gene: [11p13/CD44] antigen CD44 (gp90; lymphocyte homing/adhesion receptor; lethal antigen 3); antigen MDU2 (MDU3; monoclonal antibodies A1G3, A3D8); antigen MIC4 (monoclonal antibodies F10.44.2, mab4); Lutheran blood group inhibitor? (MIM:
  • Gene: [11p13/CD59] antigen CD59 (p18-20; homolog of mouse antigen Ly-6); antigen MIC11 (monoclonal antibody 16.3A5; MIM:143065); antigen MIN1 (monoclonal antibody EJ16); antigen MIN2 (monoclonal antibody EJ30); antigen MIN3 (monoclonal anti
  • Gene: [11p13/FRA11E] fragile site 11p13, aphidicolin type, common;
  • Gene: [11p13/FSHB] follicle stimulating hormone, beta polypeptide (follitropin beta);
  • Gene: [11p13/GUD] genitourinary dysplasia component of WAGR (gonadoblastoma); [UG GD ]
  • Gene: [11p13/HVBS1] hepatitis B virus integration site 1; liver cell carcinoma (hepatocellular carcinoma); [LCC HCC HBVS1 ]
  • Gene: [11p13/LMO2] LIM domain only 2 (rhombotin-like 1); [RBTNL1 RHOM2 ]
  • Gene: [11p13/M11S1] membrane component, chromosome 11, surface marker 1; glycosylphosphatidylinositol (GPI)-anchored membrane protein, 137kD;
  • Gene: [11p13/NFIXL4] nuclear factor I/X-like 4;
  • Gene: [11p13/PAX6] paired box homeotic gene 6 (oculorhombin); aniridia, type II (Wilms' tumor-linked); keratitis, hereditary (MIM:148190); [AN2 ]
  • Gene: [11p13/PDX1] pyruvate dehydrogenase complex, lipoyl-containing component X; protein X; lacticacidemia (due to defect in lipoyl-containing component X of pyruvate dehydrogenase complex deficiency);
  • Gene: [11p13/RAG1] recombination activating gene 1; severe combined immunodeficiency, B-cell-negative (MIM:601457); [SCID ]
  • Gene: [11p13/RAG2] recombination activating gene 2; severe combined immunodeficiency, B-cell-negative (MIM:601457); [SCID ]
  • Gene: [11p13/RCN1] reticulocalbin 1, EF-hand calcium binding domain; [Rcal ]
  • Gene: [11p13/TCL2] T cell lymphoma 2 associated breakpoint;
  • Gene: [11p13/WT1] Wilms tumor suppressor 1; Wilms tumor 1 (nephroblastoma; mesothelioma?); WAGR syndrome (MIM:194072); Denys-Drash syndrome (MIM:194080); [WAGR WTCR1 ]
  • Gene: [11p14/HSPCAL3] heat shock 90kD protein, alpha-like 3;
  • Gene: [11p14/KCNA4] potassium voltage-gated channel, shaker-related subfamily, member 4;
  • Gene: [11p142/FRA11D] fragile site 11p14.2, aphidicolin type, common;
  • Gene: [11p15/AA] atrophia areata, peripapillary chorioretinal degeneration;
  • Gene: [11p15/APBB1] amyloid beta (A4) precursor protein-binding, family B, member 1 (Fe65); retroviral integrase related; [RIR Fe65 ]
  • Gene: [11p15/ARHG] ras homolog gene family, member G (rho G); [RHOG ]
  • Gene: [11p15/ART1] ADP-ribosyltransferase 1, arginine (NADP+);
  • Gene: [11p15/ASM] adult skeletal muscle transcript (H19); [ASM1 H19 D11S ]
  • Gene: [11p15/CALCP] calcitonin pseudogene;
  • Gene: [11p15/CLN2] ceroid-lipofuscinosis, neuronal 2, late infantile (Jansky-Bielschovsky disease); amaurotic idiocy, late infantile; [LNCL LINCL ]
  • Gene: [11p15/CSNK2A1P] casein kinase 2, alpha 1 polypeptide pseudogene;
  • Gene: [11p15/EIF4G2] eukaryotic translation initiation factor 4 gamma 2; death-associated protein 5; [DAP5 p97 ]
  • Gene: [11p15/GLULL2] glutamate-ammonia ligase (glutamine synthase)-like 2;
  • Gene: [11p15/HPX] hemopexin (beta-1B-glycoprotein);
  • Gene: [11p15/ILK] integrin-linked kinase;
  • Gene: [11p15/KRN1L] keratin, cuticle, ultrahigh sulphur 1-like;
  • Gene: [11p15/NELL1] nel (chicken)-like 1;
  • Gene: [11p15/NUP98] nucleoporin, 98kD;
  • Gene: [11p15/PDE3B] phosphodiesterase 3B, cGMP-inhibited; cyclic-AMP phosphodiesterase, adipocyte, cGMP-inhibited;

    •