Symbol Name ID |
Tprn
taperin MGI:2139535 |
* | Aspects of the system are reported to show a normal phenotype. |
Darker colors indicate more annotations |
Human Phenotypes | Sensorineural hearing impairment |
Progressive sensorineural hearing impairment |
Disease(s) Associated with TPRN | ||
autosomal recessive nonsyndromic deafness 79 |
Mouse Phenotypes | hearing/vestibular/ear phenotype |
decreased inner hair cell stereocilia number |
decreased outer hair cell stereocilia number |
cochlear inner hair cell degeneration |
cochlear outer hair cell degeneration |
abnormal auditory brainstem response |
increased or absent threshold for auditory brainstem response |
nonsyndromic hearing loss |
|
Availability | Mouse Genotype | ||||||||
Tprnem1Pghu/Tprnem1Pghu | * | ||||||||
Tprntm1.1(KOMP)Vlcg/Tprntm1.1(KOMP)Vlcg |
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 08/02/2024 MGI 6.24 |
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