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Protein-coding gene in the species Homo sapiens From Wikipedia, the free encyclopedia
Potassium channel subfamily K member 1 is a protein that in humans is encoded by the KCNK1 gene.[5][6][7]
KCNK1 | |||||||||||||||||||||||||||||||||||||||||||||||||||
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Identifiers | |||||||||||||||||||||||||||||||||||||||||||||||||||
Aliases | KCNK1, DPK, HOHO, K2P1, K2p1.1, KCNO1, TWIK-1, TWIK1, potassium two pore domain channel subfamily K member 1 | ||||||||||||||||||||||||||||||||||||||||||||||||||
External IDs | OMIM: 601745; MGI: 109322; HomoloGene: 1691; GeneCards: KCNK1; OMA:KCNK1 - orthologs | ||||||||||||||||||||||||||||||||||||||||||||||||||
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Wikidata | |||||||||||||||||||||||||||||||||||||||||||||||||||
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This gene encodes K2P1.1, a member of the superfamily of potassium channel proteins containing two pore-forming P domains. The product of this gene has not been shown to be a functional channel, however, and it may require other non-pore-forming proteins for activity.[7]
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