KCNK7

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

Potassium channel, subfamily K, member 7, also known as KCNK7 or K2P7.1 is a protein which is encoded in humans by the KCNK7 gene. K2P7.1 is a potassium channel containing two pore-forming P domains.[5][6][7] Multiple transcript variants encoding different isoforms have been found for this gene.[8]

AliasesKCNK7, K2p7.1, TWIK3, potassium two pore domain channel subfamily K member 7
End65,595,996 bp[1]
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KCNK7
Identifiers
AliasesKCNK7, K2p7.1, TWIK3, potassium two pore domain channel subfamily K member 7
External IDsOMIM: 603940; MGI: 1341841; HomoloGene: 43131; GeneCards: KCNK7; OMA:KCNK7 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_033456
NM_005714
NM_033347
NM_033348
NM_033455

NM_001004138
NM_010609

RefSeq (protein)

NP_005705
NP_203133
NP_203134
NP_258416

NP_034739

Location (UCSC)Chr 11: 65.59 – 65.6 MbChr 19: 5.75 – 5.76 Mb
PubMed search[3][4]
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Function

This gene encodes 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; It may require other non-pore-forming proteins for activity.[8]

See also

References

Further reading

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