|
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 |
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| 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) |
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last database update 05/19/2026 MGI 6.24 |
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