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Symbol Name ID Chromosome |
D7Cwr18
DNA segment, Chr 7, Case Western Reserve 18 MGI:93877 7 |
| 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:11039 Niswander L, et al., Molecular mapping of albino deletions associated with early embryonic lethality in the mouse. Genomics. 1991 Jan;9(1):162-9 | |
| TEXT | 7 | J:15677 Rinchik EM, et al., Molecular analysis of radiation-induced albino (c)-locus mutations that cause death at preimplantation stages of development. Genetics. 1993 Dec;135(4):1107-16 | |
| TEXT | 7 | J:2638 Schedl A, et al., Chromosome jumping from flanking markers defines the minimal region for alf/hsdr-1 within the albino-deletion complex. Genomics. 1992 Oct;14(2):288-97 | |
| TEXT-Physical Mapping | 7 | J:2635 Kelsey G, et al., Physical mapping of the albino-deletion complex in the mouse to localize alf/hsdr-1, a locus required for neonatal survival. Genomics. 1992 Oct;14(2):275-87 |
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 12/10/2024 MGI 6.24 |
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