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.
Search for: (from the current location)    
  • Enter gene symbol, chromosomal location, or disorder keyword to search for, e.g. "CYP1", "5", "1pter", "Xq", or "alzheimer".
  • You must capitalize X and Y to search for those chromosomes.
7q33-q35, ARHGEF5 to 7q35, FASTK <<Move Up Move Down>>
Location Symbol Title MIM # Disorder Comments Method Mouse
7q33-q35 ARHGEF5, TIM Rho guanine nucleotide exchange factor-5 (oncogene TIM)   600888     REa, A  
7q33-q35 EPHB6, HEP Ephrin receptor EPHB6   602757     A  
7q33-q35 MTPN Myotrophin   606484     A  
7q34 BRAF Murine sarcoma viral (v-raf) oncogene homolog B1   164757 Melanoma, melignant, somatic (3); Colorectal cancer, somatic (3);Adenocarcinoma of lung, somatic, 211980 (3); Nonsmall cell lung cancer, somatic (3); Cardiofaciocutaneous syndrome, 115150 (3) pseudogene BRAF2 on Xq13 or 7q A, REa 10(Braf)
7q34 LUC7L2 Luc7, S. cerevisiae, homolog of, 2   613056     REc, H 6(Luc7l2)
7q34 MGAM, MGA Maltase-glucoamylase   154360   similar to EST GS1365 REc  
7q34 PARP12, ZC3HDC1, FLJ22693 Poly(ADP-ribose) polymerase family, member 12   612481     REc  
7q34 SSBP1, SSBP Single-stranded DNA-binding protein 1   600439     Psh, A  
7q34 SVOPL SV2-related protein-like   611700     REc 6(Svopl)
7q34 TBXAS1, GHOSAL, CYP5 Thromboxane A synthase 1, platelet   274180 Thromboxane synthase deficiency (2); Ghosal syndrome, 231095 (3)   A, Fd 6(Tbxas1)
7q34 TPK1 Thiamine pyrophosphokinase   606370     A  
7q34 ZC3HAV1, ZAP, FLJ13288, FLB6421 Zinc finger CCCH domain-containing antiviral protein 1   607312     REc 6(Zap)
7q34-q35 ZYX Zyxin   602002     Psh, A  
7q34-q36 DFNB13 Deafness, autosomal recessive 13   603098 Deafness, autosomal recessive 13 (2)   Fd  
7q34-q36 OTSC2 Otosclerosis 2   605727 Otosclerosis-2 (2)   Fd  
7q35 ACCN3, ASIC3, TNAC1, DRASIC Cation channel, amiloride-sensitive, neuronal 3   611741     R  
7q35 AKR1B1, ALDR1 Aldo-keto reductase family 1, member B1   103880     REa, A  
7q35 CLCN1 Chloride channel-1, skeletal muscle   118425 Myotonia congenita, recessive, 255700 (3); Myotonia congenita,dominant, 160800 (3); Myotonia levior, recessive (3)   H, REa, Fd 6(adr, Clc1)
7q35 CASP2, NEDD2, ICH1 Caspase 2, apoptosis-related cysteine protease (neural precursor cell expressed, developmentally down-regulated 2) 600639     R  
7q35 EZH2, EZH1 Enhancer of zeste, Drosophila, homolog of, 2   601573   pseudogene on 21q22 REc, Psh, A 6(Ezh2)
7q35 FASTK, FAST Fas-activated serine/threonine kinase   606965     R, REc  
Copyright © 1966-2009 Johns Hopkins University <<Move Up Move Down>>

Disclaimer | Write to the Help Desk | Privacy Policy
NCBI | NLM | NIH