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.
Search for: (from the current location)    
  • Enter gene symbol, chromosomal location, or disorder keyword to search for, e.g. "CYP1", "5", "1pter", "Xq", or "alzheimer".
  • You must capitalize X and Y to search for those chromosomes.
17q21.32, ITGA2B to 17q22, NOG <<Move Up Move Down>>
Location Symbol Title MIM # Disorder Comments Method Mouse
17q21.32 ITGA2B, GP2B, CD41B Integrin, alpha-2b (platelet glycoprotein IIb of IIb/IIIa complex, antigen CD41B) 607759 Glanzmann thrombasthenia, type A, 273800 (3); Thrombocytopenia,neonatal alloimmune (1) 3' to GP3A; BAK platelet antigen A, REb, REa, RE, F, LD  
17q21.32 ITGB3, GP3A Integrin, beta-3 (platelet glycoprotein IIIa; antigen CD61)   173470 Glanzmann thrombasthenia, type B (3) in same 260kb fragment as GP2B; PL(A) platelet antigen REa, REb, A, RE, F, LD  
17q21.32 MYST2, HBO1 Histone acetyltransferase MYST2   609880     R, REc  
17q21.32 PNPO Pyridoxamine 5'-phosphate oxidase   603287 Pyridoxamine 5'-phosphate oxidase deficiency, 610090 (3)   REc, H 11(Pnpo)
17q21.32 RCCP3 Renal cell carcinoma, papillary, 3   605075 Renal cell carcinoma, papillary, 3 (2) duplication in 17q21 Ch, A  
17q21.32 SNF8, VPS22, EAP30 SNF8, S. cerevisiae, homolog of   610904     R, REc  
17q21.32 TTLL6 Tubulin tyrosine ligase-like family, member 6   610849     REc  
17q21.33 ACSF2, FLJ20920 Acyl-CoA synthetase family member 2   610465     R, REc  
17q21.33 CHAD Chondroadherin   602178     Psh, A  
17q21.33 HILS1 Spermatid-specific linker histone H1-like protein   608101     REc 11(Hils1)
17q21.33 SLC35B1, UGTREL1 Solute carrier family 35, member B1   610790     R, REc  
17q21.33 SPAG9, SYD1, KIAA0516 Sperm-associated antigen 9   605430     R, REc  
17q21.33 UTP18 UTP18, S. cerevisiae, homolog of   612816     REc  
17q22 ABCC3, CMOAT2, MRP3, MLP2 ATP-binding cassette, sub-family C, member 3   604323     R, A  
17q22 BCL5 B-cell CLL/lymphoma-5   151441     REa, A  
17q22 BRIP1, BACH1, FANCJ BRCA1-associated C-terminal helicase 1   605882 Breast cancer, early-onset, 114480 (3); Fanconi anemia,complementation group J, 609054 (3) ?or 17q23 REc, Fd  
17q22 CACNA1G Calcium channel, voltage-dependent, T type, alpha-1G subunit   604065     A, R, H 11(Cacna1g)
17q22 COX11 Cytochrome c oxidase, subunit 11   603648   pseudogene on 6p23-p22 REa  
17q22 DGKE Diacylglycerol kinase, epsilon, 64-kD   601440     A, R  
17q22 HLF Hepatic leukemia factor   142385     Ch, R  
17q22 NOG, SYM1, SYNS1 Noggin, mouse, homolog of   602991 Symphalangism, proximal, 185800 (3); Synostoses syndrome, multiple,1, 186500 (3); Tarsal-carpal coalition syndrome, 186570 (3); Stapes ankylosis with broad thumb and toes, 184460 (3); Brachydactyly, type B2, 611377 (3)   A, R, Fd  
Copyright © 1966-2009 Johns Hopkins University <<Move Up Move Down>>

Disclaimer | Write to the Help Desk | Privacy Policy
NCBI | NLM | NIH