|
Symbol Name ID |
Pkhd1l1
polycystic kidney and hepatic disease 1-like 1 MGI:2183153 |
Excel File
| Allelic Composition Genetic Background |
Annotated Term | Reference |
| Pkhd1l1tm2c(EUCOMM)Hmgu/Pkhd1l1tm2c(EUCOMM)Hmgu Gfi1tm1(cre)Gan/Gfi1+ involves: 129S4/SvJaeSor * 129S7/SvEvBrd * C57BL/6N |
prenatal lethality, complete penetrance | J:280240 |
| Pkhd1l1tm2c(EUCOMM)Hmgu/Pkhd1l1tm2c(EUCOMM)Hmgu Tg(Atoh1-cre)1Bfri/0 involves: 129S4/SvJaeSor * C57BL/6 * C57BL/6N * CBA |
abnormal distortion product otoacoustic emission | J:280240 |
| abnormal outer hair cell stereociliary bundle morphology | J:280240 | |
| abnormal tectorial membrane morphology | J:280240 | |
| decreased outer hair cell stereocilia number | J:280240 | |
| impaired hearing | J:280240 | |
| increased or absent threshold for auditory brainstem response | J:280240 |
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 04/16/2024 MGI 6.23 |
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