KCNJ2

Jump to: navigation, search
potassium inwardly-rectifying channel, subfamily J, member 2
Identifiers
SymbolKCNJ2
Entrez3759
HUGO6263
OMIM600681
RefSeqNM_000891
UniProtP63252
Other data
LocusChr. 17 q23.1-24.2

KCNJ2 (Kir2.1) is a gene encoding an inward-rectifier potassium ion channel.

Clinical significance

A defect in this gene is associated with Andersen-Tawil syndrome.

External links




Linked-in.jpg