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.
17q25, EVPL to 17q25, SEPT9 <<Move Up Move Down>>
Location Symbol Title MIM # Disorder Comments Method Mouse
17q25 EVPL Envoplakin   601590     REa, A  
17q25 FASN Fatty acid synthase   600212     A  
17q25 FN3KRP Fructosamine 3-kinase-related protein   611683     REc  
17q25 FSCN2, RFSN, RP30 Fascin, sea urchin, homolog of, 2   607643 Retinitis pigmentosa-30, 607921 (3) within 200kb of ACTG1 A, REc  
17q25 PSORS2, PSS1 Psoriasis susceptibility 2   602723 {Psoriasis, susceptibility to}, 177900 (2) about 50% of families linked to 17q; not confirmed by some Fd  
17q25 GCGR Glucagon receptor   138033 {Diabetes mellitus, noninsulin-dependent}, 125853 (3)   A, Fd  
17q25 GRIN2C, NMDAR2C Glutamate receptor, ionotropic, N-methyl D-aspartate 2C   138254     A  
17q25 H3F3B H3 histone, family 3B (H3.3B)   601058     A  
17q25 HGS, HRS Human growth factor-regulated tyrosine kinase substrate   604375     REa, A  
17q25 ILF1 Interleukin enhancer-binding factor 1   147685     REa, A  
17q25 JMJD6, PSR Jumonji domain containing 6 (phosphatidylserine receptor)   604914     REc  
17q25 KCNJ16, KIR5.1 Potassium channel, inwardly rectifying, subfamily J, member 16   605722     R  
17q25 LGALS3BP Lectin, galactoside-binding, soluble, 3 binding protein (galectin 6 binding protein) 600626     A 11(Lgals3bp)
17q25 MAFG v-maf avian musculoaponeurotic fibrosarcoma oncogene family, protein G   602020     A  
17q25 MYMY2 Moyamoya disease 2   607151 Moyamoya disease 2 (2) ?3p26; between D17S785 and D17S836 Fd  
17q25 P4HB, PROHB Procollagen-proline, 2-oxoglutarate-4-dioxygenase, beta polypeptide; thyroid hormone-binding protein p55 176790     S, REa, A, C  
17q25 PDE6G, PDEG Phosphodiesterase-6G, cGMP-specific, rod, gamma   180073     REa, A, Fd 11(Pdeg)
17q25 PCNT1, PCNT Pericentrin 1   170285     REc  
17q25 RECQL5, RECQ5 DNA helicase, RecQ-like, type 5   603781     A  
17q25 RFNG Radical fringe   602578     REa 11(Rfng)
17q25 SEPT9, MSF, MSF1, NAPB Septin 9   604061 Leukemia, acute myeloid, therapy-related (1); Ovarian carcinoma (1);Amyotrophy, hereditary neuralgic, 162100 (3)   Ch, REa, Fd  
Copyright © 1966-2009 Johns Hopkins University <<Move Up Move Down>>

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