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KCNJ10, potassium inwardly rectifying channel subfamily J member 10

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KCNJ10, potassium inwardly rectifying channel subfamily J member 10

  • This gene encodes a member of the inward rectifier-type potassium channel family, characterized by having a greater tendency to allow potassium to flow into, rather than out of, a cell. The encoded protein may form a heterodimer with another potassium channel protein and may be responsible for the potassium buffering action of glial cells in the brain. Mutations in this gene have been associated with seizure susceptibility of common idiopathic generalized epilepsy syndromes. [provided by RefSeq, Jul 2008]

  • Gene Synonyms (BIRK-10, KCNJ13-PEN, KIR1.2, KIR4.1, SESAME, ATP-sensitive inward rectifier potassium channel 10, ATP-dependent inwardly rectifying potassium channel Kir4.1, glial ATP-dependent inwardly rectifying potassium channel KIR4.1, inward rectifier K(+) channel Kir1.2, inward rectifier K+ channel KIR1.2, potassium channel, inwardly rectifying subfamily J member 10, potassium voltage-gated channel subfamily J member 10,)
  • NCBI Gene ID: 3766
  • Species: Homo sapiens (Human)
  • UNIPROT ID#>>P78508
  • 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 10 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.

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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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