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Symbol
Name
ID

Clic5
chloride intracellular channel 5
MGI:1917912

Phenotype annotations related to hearing/vestibular/ear

Darker colors indicate more annotations

Human Phenotypes	Abnormal vestibular function	Vestibular areflexia	Sensorineural hearing impairment
Disease(s) Associated with CLIC5
autosomal recessive nonsyndromic deafness 103

Mouse Phenotypes		abnormal cochlear hair cell stereociliary bundle morphology	cochlear inner hair cell degeneration	cochlear outer hair cell degeneration	organ of Corti degeneration	vestibular hair cell degeneration	increased or absent threshold for auditory brainstem response	deafness
Availability	Mouse Genotype	abnormal cochlear hair cell stereociliary bundle morphology	cochlear inner hair cell degeneration	cochlear outer hair cell degeneration	organ of Corti degeneration	vestibular hair cell degeneration		deafness
	Clic5^jbg-2J/Clic5^jbg-2J
	Clic5^jbg/Clic5^jbg
	Clic5^nmf318/Clic5^nmf318

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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