Symbol Name ID |
Ripor2
RHO family interacting cell polarization regulator 2 MGI:2444879 |
* | Aspects of the system are reported to show a normal phenotype. |
Darker colors indicate more annotations |
Human Phenotypes | Abnormal vestibular function |
Sensorineural hearing impairment |
Prelingual sensorineural hearing impairment |
Disease(s) Associated with RIPOR2 | |||
autosomal dominant nonsyndromic deafness 21 | |||
autosomal recessive nonsyndromic deafness 104 |
Mouse Phenotypes | hearing/vestibular/ear phenotype |
abnormal cochlear hair cell stereociliary bundle morphology |
abnormal inner hair cell stereociliary bundle morphology |
decreased inner hair cell stereocilia number |
abnormal orientation of outer hair cell stereociliary bundles |
abnormal outer hair cell stereociliary bundle morphology |
thin cochlear hair cell stereocilia |
absent distortion product otoacoustic emissions |
impaired hearing |
deafness |
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Availability | Mouse Genotype | ||||||||||
Ripor2tm1(KOMP)Vlcg/Ripor2tm1(KOMP)Vlcg | * | ||||||||||
Ripor2tm1(KOMP)Vlcg/Ripor2+ |
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 04/16/2024 MGI 6.23 |
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