PubMed Nucleotide Protein Genome Structure PopSet Taxonomy OMIM
The OMIM Gene map presents the cytogenetic map location of disease genes and other expressed genes described in OMIM. See the OMIM Morbid Map for a list of disease genes organized by disease. For more refined maps of genes and DNA segments click on the Location to invoke NCBI Entrez Map Viewer.
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17q12-q21, WT4 to 17q21, C1QL1 <<Move Up Move Down>>
Location Symbol Title MIM # Disorder Comments Method Mouse
17q12-q21 WT4 Wilms tumor-4   601363 Wilms tumor, type 4 (2)   Fd  
17q12-q21 ZPBP2, ZPBPL Zona pellucida-binding protein 2   608499     REc  
17q12-q21.1 GGNBP2, DIF3, LCRG1, LZK1 Gametogenetin-binding protein 2   612275     REc  
17q12-q21.1 RAMP2 Receptor activity-modifying protein 2   605154     R 11(Ramp2)
17q12-q21.2 CCR7, CMKBR7, EBI1 Chemokine (C-C) receptor 7 (Epstein-Barr virus induced gene 1)   600242     REa, A  
17q12-q21.3 MLN51, CASC3 MLN51 gene   606504     A  
17q12-q21.33 SGCA, ADL, DAG2, LGMD2D, DMDA2 Sarcoglycan, alpha (50kD dystrophin-associated glycoprotein; adhalin)   600119 Muscular dystrophy, limb-girdle, type 2D, 608099 (3); Adhalinopathy,primary (1)   Psh, A  
17q12-q22 CRHR1, CRHR Corticotropin releasing hormone receptor 1   122561     Psh  
17q12-q22 PTMS Parathymosin   168440     A  
17q12-q23.2 CDC27 Cell division cycle 27   116946   between ERBB2 and PRKCA Psh, H 11(Cdc27)
17q21 ACACA, ACAC, ACC1 Acetyl-Coenzyme A carboxylase, alpha   200350 Acetyl-CoA carboxylase deficiency (1) proximal to q21.33; others put at 17q12 A  
17q21 AOC2, RAO Amine oxidase, copper-containing, 2   602268     A  
17q21 AOC3, HPAO, VAP1 Amine oxidase, copper-containing 3   603735     TM  
17q21 ARHGAP27, CAMGAP1 RHO GTPase-activating protein 27   610591     REc  
17q21 ARHN, RHO7 Ras homolog gene family, member N (GTP-binding protein Rho7) 601555     REn  
17q21 ASRT6 Asthma-related traits, susceptibility to, 6   611403 {Asthma-related traits, susceptibility to, 6} (2) strongly associated with rs7216389 Fd  
17q21 ATP6V0A1, ATP6N1A, VPP1 ATPase, H+ transporting, lysosomal, V0 subunit A1   192130     REa, REn 11(Atp6n1)
17q21 AUTS7 Autism, susceptibility to, 7   610676 {Autism, susceptibility to, 7}, 610676 (2) max lod at D17S2180 Fd  
17q21 BECN1 Beclin 1   604378     REc, A  
17q21 BRCA1, PSCP, BROVCA1 Breast cancer-1 gene   113705 {Breast-ovarian cancer, familial, 1}, 604370 (3)   Fd, REc 11(Brca1)
17q21 C1QL1, CRF, C1QRF Complement component 1, q subcomponent-like 1   611586     A  
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