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".
  • You must capitalize X and Y to search for those chromosomes.
19p12, GDF1 to 19q, CHMP2A <<Move Up Move Down>>
Location Symbol Title MIM # Disorder Comments Method Mouse
19p12 GDF1 Growth/differentiation factor 1   602880 Transposition of great arteries, dextro-looped 3 (3); Double-outletright ventricle, 217095 (3); Tetralogy of Fallot, 187500 (3)   REc  
19p12 LASS1, UOG1 Lag1, S. cerevisiae, homolog of, 1   606919     A  
19p12 LPAR2, EDG4 Lysophosphatidic acid receptor 2   605110     REc 8(Edg4)
19p12 MEF2B MADS box transcription enhancer factor 2, polypeptide B (myocyte enhancer factor 2B) 600661     REn ?8(Mef2b)
19p12 PKN1, PRKCL1, PRK1, PAK1 Protein kinase N1   601032     R, A 8(Prkcl1)
19p12 RFXANK Regulatory factor X, ankyrin repeat-containing   603200 MHC class II deficiency, complementation group B, 209920 (3)   REc  
19p12 TM6SF2, KIAA1926 Transmembrane 6 superfamily, member 2   606563     REc  
19p12 ZNF98 Zinc finger protein-98   603980     REc  
19p12 ZNF99 Zinc finger protein-99   603981     REc  
19p12-p11 GMIP GEM-interacting protein   609694     REc  
19p EXT3 Exostoses, multiple, 3   600209 Exostoses, multiple, type 3 (2)   Fd  
19p RPL18A Ribosomal protein L18a   604178     REa, R  
19p RPS15, RIG Ribosomal protein S15   180535     REa, R  
19p TMEM3, B3GNT3 Transmembrane protein 3 (beta-1,3-N-acetylglucosaminyltransferase 3)   605863     REc  
19p ZNF77 Zinc finger protein-77 (pT1)   194551     REa  
19p ZNF121, D19S204 Zinc finger protein-121 (clone ZHC32)   194628     REa, Fd  
19cen-q12 MAN2B1, MANB Mannosidase, alpha, class 2B, member 1   609458 Mannosidosis, alpha-, types I and II, 248500 (3)   S, Psh, REa 8(Man2b1)
19cen-q13.11 PEPD Peptidase D (prolidase)   170100 Prolidase deficiency (3) closely linked to APOC2 S, F, H, Fd 7(Pep4)
19cen-q13.2 A1BG Glycoprotein, alpha-1B   138670   order: C3-SE-LU-A1BG F  
19q BFIC Benign familial infantile convulsions   601764 Convulsions, benign familial infantile (2)   Fd  
19q CHMP2A, VPS2A, VPS2, BC2 CHMP family, member 2A   610893     R  
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