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Symbol
Name
ID

Mir96
microRNA 96
MGI:3619440

Phenotype annotations related to hearing/vestibular/ear

Darker colors indicate more annotations

Human Phenotypes	Sensorineural hearing impairment	Progressive sensorineural hearing impairment	Progressive hearing impairment	Tinnitus
Disease(s) Associated with MIR96
autosomal dominant nonsyndromic deafness 50

Mouse Phenotypes		decreased cochlear hair cell number	abnormal cochlear hair cell stereociliary bundle morphology	cochlear outer hair cell degeneration	cochlear hair cell degeneration	fused vestibular hair cell stereocilia	absent cochlear nerve compound action potential	decreased cochlear nerve compound action potential	impaired hearing	deafness
Availability	Mouse Genotype	decreased cochlear hair cell number	abnormal cochlear hair cell stereociliary bundle morphology	cochlear outer hair cell degeneration	cochlear hair cell degeneration	fused vestibular hair cell stereocilia	absent cochlear nerve compound action potential	decreased cochlear nerve compound action potential	impaired hearing	deafness
	Mir96^Dmdo/Mir96^Dmdo
	Mir96^Dmdo/Mir96⁺

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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