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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5q14, GPR98 to 4q21-q22, HPGDS <<Move Up Move Down>>
Location Symbol Title MIM # Disorder Comments Method Mouse
5q14 GPR98, MASS1, VLGR1, KIAA0686, FEB4, USH2C, USH2B G protein-coupled receptor 98   602851 Convulsions, familial febrile, 4, 604352 (3); Usher syndrome, typeIIC, 605472 (3)   A, REc, R, Fd 13(Frings, mass1)
4q21 ANXA3, ANX3 Annexin A3 (lipocortin III)   106490     Psh, REa, A  
4q21 ARHGAP24, RCGAP72, FILGAP RHO GTPase-activating protein 24   610586     REc  
4q21 CDS1 CDP-diacylglycerol synthase 1   603548     R, A  
4q21 CXCL9, MIG, SCYB9 Chemokine, C-X-C motif, ligand 9   601704   close to INP10 A, REn  
4q21 CXCL10, INP10 Chemokine, C-X-C motif, ligand 10 (interferon-inducible cytokine IP-10) 147310   ?involved in monocytic leukemia with t(4;11)(q21;q23) A, REa, F  
4q21 CXCL13, SCYB13, BCA1, BLC Chemokine, C-X-C motif, ligand 13   605149     REc  
4q21 DMP1, ARHR, ARHP Dentin matrix acidic phosphoprotein   600980 Hypophosphatemic rickets, AR, 241520 (3)   Fd, REn, Psh, A  
4q21 ENAM, AIH2, AI1C Enamelin   606585 Amelogenesis imperfecta, type IB, 104500 (3);Amelogenesis imperfecta, type IC, 204650 (3)   REc  
4q21 FGF5 Fibroblast growth factor-5   165190     REa, A 5(Fgf5)
4q21 FRAS1 FRAS1 gene   607830 Fraser syndrome, 219000 (3)   Fd 5(bl, Fras1)
4q21 HEL308 DNA helicase Hel308   606769     H 5(Hel308)
4q21 HIES Hyper-IgE syndrome   147060 Hyper-IgE syndrome (2)   Ch, Fd  
4q21 HSD17B11, RETSDR2, PAN1B 17-beta-hydroxysteroid dehydrogenase XI   612831     R, REc  
4q21 IGJ Immunoglobulin J polypeptide, linker protein for   147790     REa, A 5(Igj)
4q21 LGMD1G Limb-girdle muscular dystrophy, type 1G   609115 Limb-girdle muscular dystrophy, type 1G (2) max lod at D4S2964 Fd  
4q21 SLC4A4, NBC1, KNBC, SLC4A5 Solute carrier family 4, sodium bicarbonate cotransporter, member 4   603345 Renal tubular acidosis, proximal, with ocular abnormalities,604278 (3)   Psh  
4q21 SNCA, NACP, PARK1, PARK4 Synuclein, alpha (non A4 component of amyloid precursor)   163890 Parkinson disease, familial, 168601 (3); Parkinson disease 4,autosomal dominant Lewy body, 605543 (3); Dementia, Lewy body, 127750 (3)   Psh, A, Fd  
4q21 UTP3, CRL1, CRLZ1 UTP3, S. crevisiae, homolog of   611614     REc 5(Utp3)
4q21-q22 COQ2 CoQ2, S. cerevisiae, homolog of (parahydroxybenzoate-polyprenyltransferase, mitochondrial) 609825 Coenzyme Q10 deficiency, 607426 (3)   REc  
4q21-q22 HPGDS, PGDS Prostaglandin D2 synthase, hematopoietic   602598     A 3(Pgds)
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