|
Symbol Name ID Chromosome |
Krd
kidney and retinal defects MGI:99258 19 |
| Experiment Type | Details | Chromosome | Reference |
|---|---|---|---|
| TEXT | 19 | J:20807 Keller SA, et al., Kidney and retinal defects (Krd), a transgene-induced mutation with a deletion of mouse chromosome 19 that includes the Pax2 locus. Genomics. 1994 Sep 15;23(2):309-20 | |
| TEXT | 19 | J:50327 Nomura H, et al., Identification of PKDL, a novel polycystic kidney disease 2-like gene whose murine homologue is deleted in mice with kidney and retinal defects. J Biol Chem. 1998 Oct 2;273(40):25967-73 | |
| TEXT-Genetic Cross | 19 | J:54055 Ji W, et al., Identification of genes within the Krd deletion on mouse chromosome 19. Mamm Genome. 1999 Apr;10(4):399-401 |
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 05/07/2024 MGI 6.23 |
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