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Symbol
Name
ID

Kcnq4
potassium voltage-gated channel, subfamily Q, member 4
MGI:1926803

Phenotype annotations related to hearing/vestibular/ear

Darker colors indicate more annotations

Human Phenotypes	Hearing impairment	Tinnitus
Disease(s) Associated with KCNQ4	Hearing impairment	Tinnitus
autosomal dominant nonsyndromic deafness 2A

Mouse Phenotypes		cochlear outer hair cell degeneration	abnormal cochlear outer hair cell physiology	increased or absent threshold for auditory brainstem response	absent distortion product otoacoustic emissions	sensorineural hearing loss
Availability	Mouse Genotype	cochlear outer hair cell degeneration	abnormal cochlear outer hair cell physiology		absent distortion product otoacoustic emissions	sensorineural hearing loss
	Kcnq4^tm1.1Tjj/Kcnq4^tm1.1Tjj
	Kcnq4^tm1.2Tjj/Kcnq4^tm1.2Tjj
	Kcnq4^tm1.2Tjj/Kcnq4⁺

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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