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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15q11.2-q12, OCA2 to 15q13.3, NDUFAF1 <<Move Up Move Down>>
Location Symbol Title MIM # Disorder Comments Method Mouse
15q11.2-q12 OCA2, P, PED, D15S12, BOCA, EYCL3, HCL3, SHEP1 Pink-eye dilution, murine, homolog of (oculocutaneous albinism II)   611409 Albinism, oculocutaneous, type II, 203200 (3); Albinism, brownoculocutaneous, 203200 (3); [Skin/hair/eye pigmentation 1, blue/nonblue eyes], 227220 (3); [Skin/hair/eye pigmentation 1, blond/brown hair], 227220 (3) ?hypopigmentation in PWS and AS D, REa, Fd 7(p)
15q11.2-q13.1 HTGS Hypertriglyceridemia, familial   145750 {Hypertriglyceridemia, susceptibility to} (2)   Fd  
15q12 HPC7 Prostate cancer, hereditary, 7   610321 {Prostate cancer, hereditary, 7} (2)   Fd  
15q12 SNRPN Small nuclear ribonucleoprotein polypeptide N   182279 Prader-Willi syndrome, 176270 (3)   REa, D 7(Snrpn)
15q12-q15 MCOPCB2 Microphthalmia, isolated, with coloboma 2   605738 Microphthalmia, isolated, with coloboma 2 (2)   Fd  
15q13 ATD Asphyxiating thoracic dystrophy   208500 Asphyxiating thoracic dystrophy (2)   Fd  
15q13 SCZD13 Schizophrenia 13   613025 {Schizophrenia, susceptibility to, 13} (2) associated with deletion at 15q13.3 Ch  
15q13 TJP1 Tight junction protein 1 (zona occludens 1)   601009     A 7(Tjp1)
15q13-q14 FMN, LD Formin (limb deformity)   136535     REa, A, Fd, Psh 2(ld)
15q13-q14 SLC12A6, KCC3A, KCC3B, KCC3, ACCPN Solute carrier family 12 (potassium/chloride transporters), member 6   604878 Agenesis of the corpus callosum with peripheral neuropathy, 218000(3)   A, R, REa, Fd  
15q13-q14 TRPM1, MLSN1 Transient receptor potential cation channel, subfamily M, member 1 (melastatin) 603576     R 7(Mlsn1)
15q13-q15 B2MR Beta-2-microglobulin regulator   109710     D  
15q13-q15 CKTSF1B1 Cysteine knot superfamily 1, BMP antagonist 1 (Gremlin)   603054     Psh, R  
15q13-qter MAP1A, MAP1L Microtubule-associated protein 1A   600178     Psh  
15q13.1 HERC2, SHEP1 HECT domain and RCC1-like domain 2   605837 [Skin/hair/eye pigmentation 1, blue/nonblue eyes], 227220 (3);[Skin/hair/eye pigmentation 1, blond/brown hair], 227220 (3) mutations in intron 4 Psh, R, REc  
15q13.1 NDNL2, MAGEG1 Necdin-like gene 2   608243     REc, H 7(Ndnl2)
15q13.1-q15.1 CILD4 Ciliary dyskinesia, primary, 4   608646 Ciliary dyskinesia, primary, 4 (2) between D15S1012 and D15S1048 Fd  
15q13.2 ARHGAP11A, KIAA0013 RHO GTPase-activating protein 11A   610589     Psh, REc  
15q13.2 SPRED1, NFLS Sprouty-related EVH1 domain-containing protein 1   609291 Legius syndrome, 611431 (3)   REc 2(Spred1)
15q13.3 DEL15q13.3, MICRODEL15q13.3 Chromosome 15q13.3 microdeletion syndrome   612001 Chromosome 15q13.3 microdeletion syndrome (4)   Ch  
15q13.3 NDUFAF1, CIA30, CGI65 NADH-ubiquinone oxidoreductase 1 alpha subcomplex, assembly factor 1   606934     REc  
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