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KCNK13, potassium two pore domain channel subfamily K member 13

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KCNK13, potassium two pore domain channel subfamily K member 13

  • Potassium channels represent the most complex class of voltage-gated ion channels from both functional and structural standpoints. Their diverse functions include regulating neurotransmitter release, heart rate, insulin secretion, neuronal excitability, epithelial electrolyte transport, smooth muscle contraction, and cell volume. This gene encodes a potassium channel containing two pore-forming domains. This protein is an open channel that can be stimulated by arachidonic acid and inhibited by the anesthetic halothane. [provided by RefSeq, Jul 2013]

  • Gene Synonyms (K2p13.1, THIK-1, THIK1, potassium channel subfamily K member 13, K2P13.1 potassium channel, potassium channel, subfamily K, member 13, potassium channel, two pore domain subfamily K, member 13, tandem pore domain halothane-inhibited potassium channel 1, tandem pore domain potassium channel THIK-1,)
  • NCBI Gene ID: 56659
  • Species: Homo sapiens (Human)
  • UNIPROT ID#>>Q9HB14
  • 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 two pore domain channel subfamily K member 13 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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