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Symbol
Name
ID
Ush2a
usherin
MGI:1341292
Phenotype annotations related to hearing/vestibular/ear
Darker colors indicate more annotations
Human Phenotypes
Congenital sensorineural hearing impairment
Disease(s) Associated with USH2A
Usher syndrome type 2A

Mouse Phenotypes
decreased cochlear outer hair cell number
abnormal distortion product otoacoustic emission
Availability Mouse Genotype
Ush2atm1Tili/Ush2atm1Tili

Contributing Projects:
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
06/11/2019
MGI 6.14
The Jackson Laboratory