KCNK18 - Wikipedia
Potassium channel subfamily K member 18 (KCNK18), also known as TWIK-related spinal cord potassium channel (TRESK) or K 2P 18.1 is a protein that in humans is encoded by the …
KCNK18 Gene - GeneCards | KCNKI Protein | KCNKI Antibody
Mar 30, 2025 · KCNK18 (Potassium Two Pore Domain Channel Subfamily K Member 18) is a Protein Coding gene. Diseases associated with KCNK18 include Migraine With Aura 13 and …
KCNK18 potassium two pore domain channel subfamily K member 18 …
Feb 8, 2025 · Altered functional properties of a missense variant in the TRESK K(+) channel (KCNK18) associated with migraine and intellectual disability. The Background K(+) Channel …
Functional analysis of missense variants in the TRESK (KCNK18) K+ ...
Jan 27, 2012 · A loss of function mutation in the TRESK K2P potassium channel (KCNK18), has recently been linked with typical familial migraine with aura. We now report the functional …
Entry - *613655 - POTASSIUM CHANNEL, SUBFAMILY K, MEMBER 18; KCNK18 …
Two-pore domain (K2P) potassium channels, such as KCNK18, give rise to background, or leak, potassium conductance, and they regulate diverse cellular functions by adjusting both the …
KCNK18 (TRESK) genetic variants in Italian patients with migraine
Our study shows the presence of several KCNK18 gene mutations in both migraine with aura and migraine without aura. However, the precise role of this gene in migraine predisposition …
Kcnk18 potassium two pore domain channel subfamily K member …
Gene ID: 445371, updated on 8-Feb-2025. Predicted to enable calcium-activated potassium channel activity; outward rectifier potassium channel activity; and potassium ion leak channel …
Further evidence of biallelic variants in KCNK18 as a cause of ...
Introduction: KCNK18, a potassium channel subfamily K member 18 (MIM*613655), encodes for TWIK-related spinal cord K+ channel (TRESK) and is important for maintaining neuronal …
KCNK18 potassium two pore domain channel subfamily K …
Clinical resource with information about KCNK18, Migraine, with or without aura, susceptibility to, 13, and available tests. There are links to practice guidelines and authoritative resources like …
KCNK18 Biallelic Variants Associated with Intellectual Disability …
Jun 4, 2021 · Here, we report the identification of KCNK18 biallelic missense variants (p.Tyr163Asp and p.Ser252Leu) in a family characterized by three siblings affected by mild-to …