Mapping Data Summary

• Symbol: Fah
• Name: fumarylacetoacetate hydrolase
• ID: MGI:95482
• Chromosome: 7

6 mapping experiments

Experiment Type	Details	Chromosome	Reference
TEXT		7	J:67045 Aponte JL, et al., Point mutations in the murine fumarylacetoacetate hydrolase gene: Animal models for the human genetic disorder hereditary tyrosinemia type 1. Proc Natl Acad Sci U S A. 2001 Jan 16;98(2):641-5
TEXT		7	J:2947 Klebig ML, et al., Murine fumarylacetoacetate hydrolase (Fah) gene is disrupted by a neonatally lethal albino deletion that defines the hepatocyte-specific developmental regulation 1 (hsdr-1) locus. Proc Natl Acad Sci U S A. 1992 Feb 15;89(4):1363-7
TEXT		7	J:1836 Ruppert S, et al., Deficiency of an enzyme of tyrosine metabolism underlies altered gene expression in newborn liver of lethal albino mice. Genes Dev. 1992 Aug;6(8):1430-43
TEXT-Physical Mapping		7	J:68210 Wines ME, et al., Identification of mesoderm development (mesd) candidate genes by comparative mapping and genome sequence analysis. Genomics. 2001 Feb 15;72(1):88-98
TEXT-Physical Mapping		7	J:49393 Wines ME, et al., Physical localization of the mouse aryl hydrocarbon receptor nuclear translocator-2 (Arnt2) gene within the c112K deletion. Genomics. 1998 Jul 15;51(2):223-32
TEXT-QTL		7	J:27733 Nagase H, et al., Distinct genetic loci control development of benign and malignant skin tumours in mice. Nat Genet. 1995 Aug;10(4):424-9