Symbol Name ID |
Ush2a
usherin MGI:1341292 |
Darker colors indicate more annotations |
Human Phenotypes | Abnormality of the inner ear |
Conductive hearing impairment |
Abnormal vestibular function |
Vestibular areflexia |
Sensorineural hearing impairment |
Congenital sensorineural hearing impairment |
Tinnitus |
Disease(s) Associated with USH2A | |||||||
retinitis pigmentosa | |||||||
Usher syndrome | |||||||
Usher syndrome type 2 | |||||||
Usher syndrome type 2A |
Mouse Phenotypes | decreased cochlear outer hair cell number |
abnormal distortion product otoacoustic emission |
|
Availability | Mouse Genotype | ||
Ush2atm1Tili/Ush2atm1Tili |
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 04/16/2024 MGI 6.23 |
|
|