KCNK2

KCNK2
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesKCNK2, K2p2.1, TPKC1, TREK, TREK-1, TREK1, hTREK-1c, hTREK-1e, potassium two pore domain channel subfamily K member 2
External IDsOMIM: 603219; MGI: 109366; HomoloGene: 7794; GeneCards: KCNK2; OMA:KCNK2 - orthologs
Orthologs
SpeciesHumanMouse
Entrez

3776

16526

Ensembl

ENSG00000082482

ENSMUSG00000037624

UniProt

O95069

P97438

RefSeq (mRNA)

NM_001017424
NM_001017425
NM_014217

NM_001159850
NM_001281847
NM_001281848
NM_010607
NM_001357119

RefSeq (protein)

NP_001017424
NP_001017425
NP_055032

Location (UCSC)Chr 1: 215.01 – 215.24 MbChr 1: 188.94 – 189.13 Mb
PubMed search
Wikidata
View/Edit HumanView/Edit Mouse

Potassium channel subfamily K member 2, also known as TREK-1, is a protein that in humans is encoded by the KCNK2 gene.

This gene encodes K2P2.1, a lipid-gated ion channel belonging to the two-pore-domain background potassium channel protein family. This type of potassium channel is formed by two homodimers that create a channel that releases potassium out of the cell to control resting membrane potential. The channel is opened by anionic lipid, certain anesthetics, membrane stretching, intracellular acidosis, and heat. Three transcript variants encoding different isoforms have been found for this gene.