KCNK5

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

Potassium channel subfamily K member 5 is a protein that in humans is encoded by the KCNK5 gene.[5][6][7]

AliasesKCNK5, K2p5.1, TASK-2, TASK2, KCNK5b, potassium two pore domain channel subfamily K member 5
End39,229,475 bp[1]
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KCNK5
Identifiers
AliasesKCNK5, K2p5.1, TASK-2, TASK2, KCNK5b, potassium two pore domain channel subfamily K member 5
External IDsOMIM: 603493; MGI: 1336175; HomoloGene: 2773; GeneCards: KCNK5; OMA:KCNK5 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_003740

NM_021542

RefSeq (protein)

NP_003731

NP_067517

Location (UCSC)Chr 6: 39.19 – 39.23 MbChr 14: 20.19 – 20.23 Mb
PubMed search[3][4]
Wikidata
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This gene encodes K2P5.1, one of the members of the superfamily of potassium channel proteins containing two pore-forming P domains. The message for this gene is mainly expressed in the cortical distal tubules and collecting ducts of the kidney. The protein is highly sensitive to external pH and this, in combination with its expression pattern, suggests it may play an important role in renal potassium transport.[7]

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References

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