KCNK1

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

KCNK1

Potassium channel subfamily K member 1 is a protein that in humans is encoded by the KCNK1 gene.[5][6][7]

Quick Facts Available structures, PDB ...
KCNK1
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesKCNK1, DPK, HOHO, K2P1, K2p1.1, KCNO1, TWIK-1, TWIK1, potassium two pore domain channel subfamily K member 1
External IDsOMIM: 601745; MGI: 109322; HomoloGene: 1691; GeneCards: KCNK1; OMA:KCNK1 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_002245

NM_008430

RefSeq (protein)

NP_002236

NP_032456

Location (UCSC)Chr 1: 233.61 – 233.67 MbChr 8: 126.72 – 126.76 Mb
PubMed search[3][4]
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]

See also

References

Further reading

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