Kcne1 (potassium voltage-gated channel, Isk-related subfamily, member 1)

基因基本信息

Kcne1 基因表型（MGI）

Homozygotes for targeted and spontaneous null mutations exhibit head-shaking, circling, ataxia, and severe deafness associated with inner ear defects. Older mutants show increased numbers of T cells. Study of cardiac myocytes in one line revealed physiologic defects.

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