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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11q12-q14, RAB30 to 11q13, C11orf5 <<Move Up Move Down>>
Location Symbol Title MIM # Disorder Comments Method Mouse
11q12-q14 RAB30 Ras-associated protein RAB30   605693     REa, REc  
11q12.1 MED19 Mediator complex subunit 19   612385     REc  
11q12.1 OSBP Oxysterol-binding protein   167040     REa, R 19(Osbp)
11q12.1 YPEL4 Yippee-like 4   609725     REc 2(Ypel4)
11q12.1-q12.3 TIMM10, TIM10A, TIM10 Translocase of inner mitochondrial membrane 10, yeast, homolog of   602251     A, R  
11q12.1-q13.5 FNL2 Fibronectin-like-2   135610     S, A  
11q12.2 CNTF Ciliary neurotrophic factor   118945     REa, A 19(Cntf)
11q12.2 PRPF19, PRP19, PSO4, NMP200 Precursor mRNA-processing factor 19, S. cerevisiae, homolog of   608330     R, REc  
11q12.2 VPS37C Vacuolar protein sorting 37, yeast, homolog of, C   610038     R, REc  
11q12.3 EEF1G, EF1G Eukaryotic translation elongation factor 1, gamma   130593     REc  
11q12.3 SLC22A24 Solute carrier family 22, member 24   611698     REc 19(Slc22a24)
11q12.3 STX5A Syntaxin 5A   603189     REc  
11q12.3 UST6 Organic anion transporter UST6   610792     REc  
11q12.3-q13.1 MGB1, SCGB2A2 Mammaglobin 1 (secretoglobin, family 2A, member 2)   605562     A, R  
11q12.3-q13.1 UGB, CC10, CCSP, SCGB1A1 Uteroglobin (Clara-cell specific 10-kD protein; secretoglobin, family 1A, member 1) 192020 {Asthma, susceptibility to}, 600807 (3)   REa, Fd, REc, A  
11q13 ANO1, TMEM16A, FLJ10261 Anoctamin 1, calcium activated chloride channel   610108     REc 7(Tmem16a)
11q13 ARL2 ADP=ribosylation factor-like 2   601175     REc  
11q13 ARRB1 Arrestin, beta 1   107940     A  
11q13 BBS1 BBS1 gene   209901 Bardet-Biedl syndrome 1, 209900 (3)   Fd  
11q13 BSCL2, SPG17, HMN5 Seipin   606158 Lipodystrophy, congenital generalized, type 2, 269700 (3); Silverspastic paraplegia syndrome, 270685 (3); Neuropathy, distal hereditary motor, type V, 600794 (3)   Fd  
11q13 C11orf5, FON Chromosome 11 open reading frame 5   604575     REc  
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