KCNK10

Potassium Two Pore Domain Channel Subfamily K Member 10

Gene Information Card

Symbol KCNK10
Full Name Potassium Two Pore Domain Channel Subfamily K Member 10
Gene Type Protein coding
Chromosomal Location 14q31.3
NCBI Gene ID 54207 ncbi.nlm.nih.gov/gene/54207
Ensembl ID ENSG00000100427
UniProt ID P57789
OMIM ID 605873
HGNC ID 6278
Aliases K2P10.1, TREK-2, TREK2

Description

KCNK10 encodes a member of the two-pore domain potassium channel family, specifically the TREK-2 (K2P10.1) channel. This channel is a background potassium channel that contributes to the resting membrane potential and is regulated by various stimuli including mechanical stretch, intracellular pH, temperature, and volatile anesthetics. It is expressed in multiple tissues, with highest levels in the brain, and plays roles in neuronal excitability, pain perception, and neuroprotection.

Disease Associations

Disease category Pathophysiological mechanism Genomic evidence
Bipolar Disorder Altered KCNK10 expression may affect neuronal excitability and mood regulation; genetic association studies have linked polymorphisms to bipolar disorder. Evidence from case-control studies (PMID: 21572416) and GWAS (PMID: 21926972).
Major Depressive Disorder Variants in KCNK10 may contribute to altered stress response and depressive phenotypes. Association reported in genetic studies (PMID: 21926972).
Pain Disorders TREK-2 channels modulate nociceptor excitability; dysregulation may contribute to chronic pain states. Functional studies in animal models (PMID: 16990514).

Expression Profile

Tissue Expression
Tissue nTPM level
Brain 12.5 High
Heart 2.1 Low
Kidney 1.8 Low
Lung 1.5 Low
Liver 0.8 Not detected
Skeletal Muscle 0.6 Not detected
Cell Line Expression
Cell Line nTPM Notes
SH-SY5Y 8.3 Neuroblastoma cell line
HEK293 0.2 Low endogenous expression
U-87 MG 4.1 Glioblastoma cell line
Data source:Human Protein Atlas(proteinatlas.org)

Mutations & Variants

Hotspot Mutations
Variant Type Frequency Functional Description
c.101C>T (p.Thr34Met) Missense <0.01% Unknown functional effect; rare variant in population databases.
c.688G>A (p.Val230Ile) Missense <0.01% Reported in ClinVar as uncertain significance.
Mutation functional classification

Loss of Function (LOF)

No well-characterized loss-of-function mutations have been reported in KCNK10.

Gain of Function (GOF)

No well-characterized gain-of-function mutations have been reported in KCNK10.

Dominant Negative (DN)

No dominant-negative mutations have been described for KCNK10.

Pathways

Potassium Channels (Reactome: R-HSA-1296071)
Voltage gated Potassium channels (KEGG: hsa04010)

Protein Summary

The TREK-2 (K2P10.1) protein is a 538-amino acid two-pore domain potassium channel with four transmembrane segments and two pore-forming loops. It forms homodimers and functions as a background potassium channel that is activated by membrane stretch, intracellular acidosis, heat, and arachidonic acid. The channel is inhibited by G-protein coupled receptor signaling and is a target for volatile anesthetics. It is highly expressed in the central nervous system, particularly in the cortex, hippocampus, and cerebellum, where it regulates neuronal excitability and neurotransmitter release.

Related Products

Product name Cat.No. Species Gene ID
KCNK10 Knockout HEK293 Cell Line EDJ-KQ11395 Human 54207 Details Get a Quote
KCNK10 Knockout HeLa Cell Line EDJ-KQ56401 Human 54207 Details Get a Quote
KCNK10 Knockout A-549 Cell Line EDJ-KQ64893 Human 54207 Details Get a Quote
KCNK10 Knockout HCT 116 Cell Line EDJ-KQ73337 Human 54207 Details Get a Quote
Displaying Records 1 To 4 Of 4 Records
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