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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  • Enter gene symbol, chromosomal location, or disorder keyword to search for, e.g. "CYP1", "5", "1pter", "Xq", or "alzheimer".
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3pter-p21, CCK to 3p26-p25, ATP2B2 <<Move Up Move Down>>
Location Symbol Title MIM # Disorder Comments Method Mouse
3pter-p21 CCK Cholecystokinin   118440     REb, REa 9(Cck)
3pter-p21 CX3CR1, GPR13, V28 Chemokine (C-X3-C) receptor 1 (G protein-coupled receptor-13)   601470 {Rapid progression to AIDS from HIV1 infection}, 609423 (3);{Coronary artery disease, resistance to}, 607339 (3); {Macular degeneration, age-related, susceptibility to}, 603075 (3)   REa  
3pter-p14 SEP SEP transmembrane protein   601053     REa  
3p26.2 CRBN, MRT2A Cereblon   609262 Mental retardation, autosomal recessive 2A, 607417 (3) between D3S3525 and D3S1560 Fd, REc  
3p26.2 EGO Eosinophil granule ontogeny   611662     REC  
3p26.2 OGG1 8-hydroxyguanine DNA glycosylase   601982 Renal cell carcinoma, clear cell, somatic, 144700 (3)   A 6(Ogg1)
3p26.2 OXTR Oxytocin receptor   167055   3p25 by others; within 7-10kb of CAV3 A, Psh  
3p26.1 CHL1, CALL, L1CAM2 CHL1, mouse, homolog of (L1 cell adhesion molecule 2)   607416     A, D 6(Chl1)
3p26.1 EDEM, KIAA0212 ER degradation-enhancing alpha-mannosidase-like protein   607673     R  
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  
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