|potassium inwardly-rectifying channel, subfamily J, member 2|
|Locus||Chr. 17 q23.1-24.2|
KCNJ2 (Kir2.1) is a gene encoding an inward-rectifier potassium ion channel.
A defect in this gene is associated with Andersen-Tawil syndrome.
- KCNJ2+protein,+human at the US National Library of Medicine Medical Subject Headings (MeSH)
- Kir2.1+channel at the US National Library of Medicine Medical Subject Headings (MeSH)
|40x30px||This genetics article is a stub. You can help Wikipedia by expanding it.|