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Article

A null mutation of mouse Kcna10 causes significant vestibular and mild hearing dysfunction.

Hearing research - 1 Jun 2013

Lee Sue I, Conrad Travis, Jones Sherri M, Lagziel Ayala, Starost Matthew F, Belyantseva Inna A, Friedman Thomas B, Morell Robert J

Abstract excerpt

KCNA10 is a voltage gated potassium channel that is expressed in the inner ear. The localization and function of KCNA10 was studied in a mutant mouse, B6-Kcna10(TM45), in which the single protein coding exon of Kcna10 was replaced with a beta-galactosidase reporter cassette. Under the regulatory...

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Source

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Identifiers

PMID: 23528307
DOI: 10.1016/j.heares.2013.02.009
PMCID: PMC3684051

Genes

KCNA10
ABR

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-23528307-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

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