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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1p36, CLCNKA to 1p36, NPHP4 <<Move Up Move Down>>
Location Symbol Title MIM # Disorder Comments Method Mouse
1p36 CLCNKA Chloride channel, kidney, A   602024 Bartter syndrome, type 4b, digenic, 613090 (3) 11kb from CLCNKB; simultaneous mutation in CLCNKA and CLCNKB Fd, REc  
1p36 CLCNKB Chloride channel, kidney, B   602023 Bartter syndrome, type 3, 607364 (3); Bartter syndrome, type 4,digenic, 602522 (3) unequal crossingover with CLCNKA Fd, REc  
1p36 CMM, MLM, DNS Cutaneous malignant melanoma/dysplastic nevus   155600 Malignant melanoma, cutaneous (2) some linkage studies negative; see 9p F, Fd, D  
1p36 DVL1 Dishevelled 1 (homologous to Drosophila dsh)   601365     Psh, A  
1p36 CORT Cortistatin   602784     H, R, REc 4(Cort)
1p36 DEL1p36, C1DELp36 Chromosome 1p36 deletion syndrome   607872 Chromosome 1p36 deletion syndrome (4) contiguous gene deletion syndrome Ch  
1p36 DJ1, PARK7 Oncogene DJ-1   602533 Parkinson disease 7, autosomal recessive early-onset, 606324 (3);Amyotrophic lateral sclerosis-Parkinsonism/dementia complex 2 (3)   Fd, R  
1p36 E2F2 E2F transcription factor 2   600426     A  
1p36 EYA3 Eyes absent, Drosophila, homolog of, 3   601655     A, H 4(Eya3)
1p36 FBXO2, FBX2, FBG1, NFB42 F-box only protein 2   607112     REc 4(Fbxo2)
1p36 H6PD, GDH, G6PDH Hexose-6-phosphate dehydrogenase   138090 Cortisone reductase deficiency, 604931 (3) digenic triallelic mutations with HSD11B1 S, F  
1p36 IBD7 Inflammatory bowel disease-7   605225 {Inflammatory bowel disease-7}, 266600 (2) associated with rs6426833 Fd  
1p36 ICMT Isoprenylcysteine carboxylmethyltransferase   605851     R  
1p36 LCA9 Leber congenital amaurosis 9   608553 Leber congenital amaurosis 9 (2) between D1S2667 and D1S1597 Fd  
1p36 LUZP1 Leucine zipper protein 1   601422     H, R 4(Luzp)
1p36 MAD2L2, MAD2B Mitotic arrest-deficient 2, S. cerevisiae, homolog-like 2   604094   pseudogene on 14q21-q23 R  
1p36 MIG6, RALT Mitogen-inducible gene 6   608069     R, REc  
1p36 MIR34A, MIRN34A Micro RNA 34A   611172     REc  
1p36 MS4 Multiple sclerosis, susceptiblity to, 4   612596 {Multiple sclerosis, susceptiblity to, 4} (2) associated with rs10492972 Fd  
1p36 NBPF3 Neuroblastoma breakpoint family, member 3   612992     REc, A  
1p36 NPHP4, SLSN4 Nephrocystin 4   607215 Nephronophthisis 4, 606966 (3); Senior-Loken syndrome 4, 606996 (3)   Fd, REc  
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