KCNK15

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KCNK15
Identifiers
AliasesKCNK15, K2p15.1, KCNK11, KCNK14, KT3.3, TASK-5, TASK5, dJ781B1.1, potassium two pore domain channel subfamily K member 15
External IDsOMIM: 607368 MGI: 2675209 HomoloGene: 11179 GeneCards: KCNK15
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_022358

NM_001030292

RefSeq (protein)

NP_071753

n/a

Location (UCSC)Chr 20: 44.75 – 44.75 Mbn/a
PubMed search[2][3]
Wikidata
View/Edit HumanView/Edit Mouse

Potassium channel subfamily K member 15 is a protein that in humans is encoded by the KCNK15 gene.[4][5][6][7]

This gene encodes K2P15.1, one of the members of the superfamily of potassium channel proteins containing two pore-forming P domains. K2P15.1 has not been shown to be a functional channel; however, it may require other non-pore-forming proteins for activity.[7]

See also[]

  • Tandem pore domain potassium channel

References[]

  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000124249 - Ensembl, May 2017
  2. ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  3. ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. ^ Kim D, Gnatenco C (Jun 2001). "TASK-5, a new member of the tandem-pore K(+) channel family". Biochem Biophys Res Commun. 284 (4): 923–30. doi:10.1006/bbrc.2001.5064. PMID 11409881.
  5. ^ Vega-Saenz de Miera E, Lau DH, Zhadina M, Pountney D, Coetzee WA, Rudy B (Jun 2001). "KT3.2 and KT3.3, two novel human two-pore K(+) channels closely related to TASK-1". J Neurophysiol. 86 (1): 130–42. doi:10.1152/jn.2001.86.1.130. PMID 11431495.
  6. ^ Goldstein SA, Bayliss DA, Kim D, Lesage F, Plant LD, Rajan S (Dec 2005). "International Union of Pharmacology. LV. Nomenclature and molecular relationships of two-P potassium channels". Pharmacol Rev. 57 (4): 527–40. doi:10.1124/pr.57.4.12. PMID 16382106. S2CID 7356601.
  7. ^ a b "Entrez Gene: KCNK15 potassium channel, subfamily K, member 15".

Further reading[]

External links[]

This article incorporates text from the United States National Library of Medicine, which is in the public domain.


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