- Gene Overview
- Interaction Network
- Sequence Verification
KCNK18, potassium two pore domain channel subfamily K member 18
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Potassium channels play a role in many cellular processes including maintenance of the action potential, muscle contraction, hormone secretion, osmotic regulation, and ion flow. This gene encodes a member of the superfamily of potassium channel proteins containing two pore-forming P domains and the encoded protein functions as an outward rectifying potassium channel. A mutation in this gene has been found to be associated with migraine with aura.[provided by RefSeq, Jan 2011]
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Gene Synonyms (K2p18.1, MGR13, TRESK, TRESK-2, TRESK2, TRIK, potassium channel subfamily K member 18, TWIK-related individual K+ channel, TWIK-related individual potassium channel, TWIK-related spinal cord K+ channel, TWIK-related spinal cord potassium channel, potassium channel, subfamily K, member 18, potassium channel, two pore domain subfamily K, member 18,)
- NCBI Gene ID:
338567
- Species:
Homo sapiens (Human)
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UNIPROT ID#>>Q7Z418
- View the NCBI Database
for this Gene »
Gene products are often involved in multiple pathways and networks within a living
cell. Learn more about other interacting partners.
potassium two pore domain channel subfamily K member 18 interacts with:
Paste a protein or nucleic acid sequence in the box below to confirm that it matches
this gene’s reference sequence(s). Click on a link under RELATED ORF CLONES to see
how a sequence matches to an experimentally-validated ORF clone.
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