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KCNJ18, potassium inwardly rectifying channel subfamily J member 18

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KCNJ18, potassium inwardly rectifying channel subfamily J member 18

  • This gene encodes a member of the inwardly rectifying potassium channel family. Transcription of this locus is regulated by thyroid hormone, and the encoded protein plays a role in resting membrane potential maintenance. Mutations in this locus have been associated with thyrotoxic hypokalemic periodic paralysis. [provided by RefSeq, Jan 2013]

  • Gene Synonyms (KIR2.6, TTPP2, inward rectifier potassium channel 18, inward rectifier K(+) channel Kir2.6, inwardly rectifying potassium channel 18, potassium channel, inwardly rectifying subfamily J, member 18, potassium voltage-gated channel subfamily J member 18, thyrotoxic periodic paralysis susceptibility ion channel,)
  • NCBI Gene ID: 100134444
  • Species: Homo sapiens (Human)
  • UNIPROT ID#>>B7U540
  • View the NCBI Database for this Gene »

The information on this page was collected from publicly accessible databases, and is periodically updated. Promega makes no claims to accuracy, or ownership of these genes.

Gene products are often involved in multiple pathways and networks within a living cell. Learn more about other interacting partners.

potassium inwardly rectifying channel subfamily J member 18 interacts with:

The information on this page was collected from publicly accessible databases, and is periodically updated. Promega makes no claims to accuracy, or ownership of these genes.

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.

The information on this page was collected from publicly accessible databases, and is periodically updated. Promega makes no claims to accuracy, or ownership of these genes.

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