|
Symbol Name ID |
Fgf20
fibroblast growth factor 20 MGI:1891346 |
| * | Aspects of the system are reported to show a normal phenotype. |
| Darker colors indicate more annotations |
| Human Phenotypes | Low-set ears |
| Disease(s) Associated with FGF20 | |
| renal agenesis |
| Mouse Phenotypes | hearing/vestibular/ear phenotype |
abnormal cochlear hair cell development |
abnormal cochlear hair cell morphology |
decreased cochlear hair cell number |
decreased cochlear outer hair cell number |
abnormal cochlear inner hair cell morphology |
abnormal organ of Corti morphology |
decreased organ of Corti supporting cell number |
abnormal pillar cell morphology |
increased or absent threshold for auditory brainstem response |
deafness |
|
| Availability | Mouse Genotype | |||||||||||
| Fgf20tm1.1Dor/Fgf20tm1.1Dor | * | |||||||||||
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO) |
||
|
Citing These Resources Funding Information Warranty Disclaimer, Privacy Notice, Licensing, & Copyright Send questions and comments to User Support. |
last database update 04/30/2024 MGI 6.23 |
|
|
|
||
Analysis Tools