Kcnq4 Phenotype Annotations

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Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

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

5 phenotypes from 2 alleles in 1 genetic background

Allelic Composition Genetic Background	Annotated Term	Reference
Kcnq4^tm1.1Tjj/Kcnq4^tm1.1Tjj involves: 129/Sv * C57BL/6	cochlear outer hair cell degeneration	J:105924
	increased or absent threshold for auditory brainstem response	J:105924
	sensorineural hearing loss	J:105924
Kcnq4^tm1.2Tjj/Kcnq4⁺ involves: 129/Sv * C57BL/6	cochlear outer hair cell degeneration	J:105924
	increased or absent threshold for auditory brainstem response	J:105924
	sensorineural hearing loss	J:105924
Kcnq4^tm1.2Tjj/Kcnq4^tm1.2Tjj involves: 129/Sv * C57BL/6	abnormal cochlear outer hair cell physiology	J:105924
	absent distortion product otoacoustic emissions	J:105924
	cochlear outer hair cell degeneration	J:105924
	increased or absent threshold for auditory brainstem response	J:105924
	sensorineural hearing loss	J:105924

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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