KCNK17

Protein-coding gene in the species Homo sapiens From Wikipedia, the free encyclopedia

Potassium channel subfamily K member 17 is a protein that in humans is encoded by the KCNK17 gene.[3][4]

AliasesKCNK17, K2p17.1, TALK-2, TALK2, TASK-4, TASK4, potassium two pore domain channel subfamily K member 17
End39,314,461 bp[1]
Quick facts Identifiers, Aliases ...
KCNK17
Identifiers
AliasesKCNK17, K2p17.1, TALK-2, TALK2, TASK-4, TASK4, potassium two pore domain channel subfamily K member 17
External IDsOMIM: 607370; HomoloGene: 88928; GeneCards: KCNK17; OMA:KCNK17 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_001135111
NM_031460

n/a

RefSeq (protein)

NP_001128583
NP_113648

n/a

Location (UCSC)Chr 6: 39.3 – 39.31 Mbn/a
PubMed search[2]n/a
Wikidata
View/Edit Human
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This gene encodes K2P17.1, one of the members of the superfamily of potassium channel proteins containing two pore-forming P domains. This open channel, primarily expressed in the pancreas, is activated at alkaline pH.[4]

See also

References

Further reading

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