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Symbol
Name
ID
Ripor2
RHO family interacting cell polarization regulator 2
MGI:2444879
Phenotype annotations related to hearing/vestibular/ear
*Aspects of the system are reported to show a normal phenotype.
Darker colors indicate more annotations
Human Phenotypes
Prelingual sensorineural hearing impairment
Disease(s) Associated with RIPOR2
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
Availability Mouse Genotype
Ripor2tm1(KOMP)Vlcg/Ripor2tm1(KOMP)Vlcg *
Ripor2tm1(KOMP)Vlcg/Ripor2+

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
02/12/2019
MGI 6.13
The Jackson Laboratory