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.
3p26.1-p25.3, SCA15 to 3p26-p24, LMCD1 <<Move Up Move Down>>
Location Symbol Title MIM # Disorder Comments Method Mouse
3p26.1-p25.3 SCA15 Spinocerebellar ataxia 15   606658 Spinocerebellar ataxia 15 (2) between D3S1620 and D3S3691 Fd  
3p26.1-p25.2 GRM7, MGLUR7 Glutamate receptor, metabotropic, 7   604101     R  
3p26.1-p25.1 ARHI2 Age-related hearing impairment 2   612976 {Age-related hearing impairment 2} (2) associated with rs11928865, rs779701, and rs779706 Fd  
3p26 BHLHB2, STRA13, DEC1 Basic helix-loop-helix domain-containing protein, class B, 2   604256     A  
3p26 CNTN3, PANG Contactin 3 (plasmocytoma-associated neuronal glycoprotein)   601325     REa, H 6(Pang)
3p26 HPC5 Prostate cancer, hereditary, 5   609299 {Prostate cancer, hereditary, 5}, 176807 (2) between D3S1270 and D3S4559 Fd  
3p26 IBD9 Inflammatory bowel disease 9   608448 {Inflammatory bowel disease-9}, 266600 (2)   Fd  
3p26 SCA29, CLA4 Spinocerebellar ataxia 29   117360 Spinocerebellar ataxia 29 (2)   Fd  
3p26 SETMAR, METNASE SET and Mariner transposase domains-containing protein   609834     REc  
3p26 STQTL5 Stature quantitative trait locus 5   608982 {Stature QTL 5} (2) max lod between D3S1297 and D3S1304 Fd  
3p26 SUMF1, FGE Sulfatase-modifying factor-1   607939 Multiple sulfatase deficiency, 272200 (3)   REc, H 6(Sumf1)
3p26-p25 ATP2B2, PMCA2 ATPase, Ca++ transporting, plasma membrane, 2   108733 {Deafness, autosomal recessive 12, modifier of}, 601386 (3)   REa  
3p26-p25 BRPF1, BR140 Bromodomain- and PHD finger-containing protein 1, 140kD   602410     A  
3p26-p25 CNTN4 Contactin 4   607280     REc, Fd  
3p26-p25 CNTN6, NB3 Contactin 6   607220     A  
3p26-p25 GHRL Ghrelin   605353 {Obesity, susceptibility to}, 601665 (3)   REc  
3p26-p25 ITPR1, SCA15, SCA16 Inositol 1,4,5-triphosphate receptor, type 1   147265 Spinocerebellar ataxia 15, 606658 (3)   REa, A 6(Itpr1)
3p26-p25 VHL VHL gene   608537 von Hippel-Lindau syndrome, 193300 (3); Renal cell carcinoma,somatic, 144700 (3); Pheochromocytoma, 171300 (3); Hemangioblastoma, cerebellar, somatic (3); Polycythemia, benign familial, 263400 (3)   Fd, D, RE  
3p26-p24.2 MYMY1, MYMY Moyamoya disease   252350 Moyamoya disease (2) max lod at D3S3050 Fd  
3p26-p24 IL5RA Interleukin-5 receptor, alpha   147851     REa, A 6(Il5r)
3p26-p24 LMCD1 LIM and cysteine-rich domains 1   604859     R 6(Lmcd1)
Copyright © 1966-2009 Johns Hopkins University <<Move Up Move Down>>

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