KCNJ12
Protein-coding gene in the species Homo sapiens
From Wikipedia, the free encyclopedia
ATP-sensitive inward rectifier potassium channel 12 is a lipid-gated ion channel that in humans is encoded by the KCNJ12 gene.[5][6][7][8][9]
AliasesKCNJ12, IRK-2, IRK2, KCNJN1, Kir2.2, Kir2.2v, hIRK, hIRK1, hkir2.2x, kcnj12x, potassium voltage-gated channel subfamily J member 12, potassium inwardly rectifying channel subfamily J member 12
External IDsOMIM: 602323; MGI: 108495; HomoloGene: 7793; GeneCards: KCNJ12; OMA:KCNJ12 - orthologs
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| Aliases | KCNJ12, IRK-2, IRK2, KCNJN1, Kir2.2, Kir2.2v, hIRK, hIRK1, hkir2.2x, kcnj12x, potassium voltage-gated channel subfamily J member 12, potassium inwardly rectifying channel subfamily J member 12 | ||||||||||||||||||||||||||||||||||||||||||||||||||
| External IDs | OMIM: 602323; MGI: 108495; HomoloGene: 7793; GeneCards: KCNJ12; OMA:KCNJ12 - orthologs | ||||||||||||||||||||||||||||||||||||||||||||||||||
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Function
This gene encodes an inwardly rectifying K+ channel that may be blocked by divalent cations. This protein is thought to be one of multiple inwardly rectifying channels that contribute to the cardiac inward rectifier current (IK1). The gene is located within the Smith–Magenis syndrome region on chromosome 17.[9]