Symbol Name ID Chromosome |
Fah
fumarylacetoacetate hydrolase MGI:95482 7 |
Experiment Type | Details | Chromosome | Reference |
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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 |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO) |
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last database update 08/21/2024 MGI 6.24 |
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