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Symbol
Name
ID
Grxcr2
glutaredoxin, cysteine rich 2
MGI:2685697
Phenotype annotations related to hearing/vestibular/ear
Darker colors indicate more annotations
Human Phenotypes
Abnormal vestibular function
Bilateral sensorineural hearing impairment
Disease(s) Associated with GRXCR2
autosomal recessive nonsyndromic deafness 101

Mouse Phenotypes
abnormal outer hair cell kinocilium morphology
abnormal cochlear hair cell stereociliary bundle morphology
abnormal orientation of cochlear hair cell stereociliary bundles
abnormal orientation of outer hair cell stereociliary bundles
abnormal outer hair cell stereociliary bundle morphology
increased or absent threshold for auditory brainstem response
abnormal distortion product otoacoustic emission
impaired hearing
reduced linear vestibular evoked potential
Availability Mouse Genotype
Grxcr2tm1.1Dck/Grxcr2tm1.1Dck
Grxcr2tm1Dck/Grxcr2tm1Dck

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
05/14/2024
MGI 6.23
The Jackson Laboratory