Kir2.6

The Kir2.6 also known as inward rectifier potassium channel 18 is a protein that in humans is encoded by the KCNJ18 gene.[1] Kir2.6 is an inward-rectifier potassium ion channel.

potassium inwardly-rectifying channel, subfamily J, member 18
Identifiers
SymbolKCNJ18
NCBI gene100134444
HGNC39080
OMIM613236
RefSeqNM_001194958
UniProtB7U540
Other data
LocusChr. 17 p11.2

Function

Inwardly rectifying potassium channels, such as Kir2.6, maintain resting membrane potential in excitable cells and aid in repolarization of cells following depolarization. Kir2.6 is primarily expressed in skeletal muscle and is transcriptionally regulated by thyroid hormone.[1]

Clinical signifiance

Mutations in this gene have been linked to thyrotoxic periodic paralysis.[1]

References

This article incorporates text from the United States National Library of Medicine, which is in the public domain.

This article is issued from Wikipedia. The text is licensed under Creative Commons - Attribution - Sharealike. Additional terms may apply for the media files.