Kir6.2
Protein-coding gene in the species Homo sapiens / From Wikipedia, the free encyclopedia
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Kir6.2 is a major subunit of the ATP-sensitive K+ channel, a lipid-gated inward-rectifier potassium ion channel.[5] The gene encoding the channel is called KCNJ11 and mutations in this gene are associated with congenital hyperinsulinism.[6]
Quick Facts KCNJ11, Identifiers ...
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