KCNJ6 Gene

potassium channel, inwardly rectifying subfamily J, member 6

This gene encodes a member of the G protein-coupled inwardly-rectifying potassium channel family of inward rectifier potassium channels. This type of potassium channel allows a greater flow of potassium into the cell than out of it. These proteins modulate many physiological processes, including heart rate in cardiac cells and circuit activity in neuronal cells, through G-protein coupled receptor stimulation. Mutations in this gene are associated with Keppen-Lubinsky Syndrome, a rare condition characterized by severe developmental delay, facial dysmorphism, and intellectual disability. [provided by RefSeq, Apr 2015]

KCNJ6-AS1 Gene

KCNJ6 antisense RNA 1

kcnj6 Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term kcnj6 in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

KCNJ6 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for KCNJ6 from the Pathway Commons Protein-Protein Interactions dataset.

G protein complex (Gngt2, Kcnj6, Gnb1) Gene Set

From CORUM Protein Complexes

proteins in the G protein complex (Gngt2, Kcnj6, Gnb1) protein complex from the CORUM Protein Complexes dataset.