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Symbol
Name
ID

Kcnq1
potassium voltage-gated channel, subfamily Q, member 1
MGI:108083

Phenotype annotations related to nervous system

Darker colors indicate more annotations

Human Phenotypes	Stroke
Disease(s) Associated with KCNQ1	Stroke
familial atrial fibrillation

Mouse Phenotypes		absent cochlear hair cells	cochlear inner hair cell degeneration	cochlear outer hair cell degeneration	absent vestibular hair cells	absent vestibular hair cell stereocilia	cochlear ganglion degeneration
Availability	Mouse Genotype	absent cochlear hair cells	cochlear inner hair cell degeneration	cochlear outer hair cell degeneration	absent vestibular hair cells	absent vestibular hair cell stereocilia	cochlear ganglion degeneration
	Kcnq1^tm1Apf/Kcnq1^tm1Apf
	Kcnq1^tm1Kpfe/Kcnq1^tm1Kpfe
	Kcnq1^tm2Kpfe/Kcnq1^tm2Kpfe

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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