Kcnj6 (potassium inwardly-rectifying channel, subfamily J, member 6)

基因基本信息

Kcnj6 基因表型（MGI）

A spontaneous mutation exhibits small size, ataxia, hypotonia, high periweaning mortality, Purkinje cell defects, and male sterility. Homozygotes for a targeted null mutation exhibit increased susceptibility to spontaneous and drug-induced seizures.

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