potassium channel 2 is a protein that in humans is encoded by the KCNJ6 gene. Mutation in KCNJ6 gene has been proposed to be the cause of Keppen-Lubinsky Syndrome...

encoding potassium voltage-gated channel, Isk-related family, member 2 KCNJ6: encoding G protein-activated inward rectifier potassium channel 2 KCNJ15:...

is caused by mutation in the inwardly rectifying K+ channels encoded by KCNJ6 gene. Gorlin, Robert; Cohen, M. Michael; Hennekam, Raoul (2001). "Syndromes...

Mutations that disrupt another inwardly rectifying K+ channel Girk2 encoded by KCNJ6 cause Keppen-Lubinsky syndrome which includes microcephaly, a narrow nasal...

1 GIRK1, KGA Kir3.2, Kir3.4, Kir3.5, Kir3.1 is not functional by itself KCNJ6 Kir3.2 GIRK2 Kir3.1, Kir3.3, Kir3.4 to form heteromeric channel KCNJ9 Kir3...

HGNC:6264 P48549 8014 KCNJ4 HGNC:6265 P48050 8015 KCNJ5 HGNC:6266 P48544 8016 KCNJ6 HGNC:6267 P48051 8017 KCNJ8 HGNC:6269 Q15842 8018 KCNJ9 HGNC:6270 Q92806...

with Down syndrome and may be related to G protein-gated ion channels. The KCNJ6 gene is located on chromosome 21 and encodes for the GIRK2 protein subunit...

potassium inwardly rectifying channel, subfamily J, member 6 Identifiers Symbol KCNJ6 Alt. symbols KCNJ7, Kir3.2, GIRK2, KATP2, BIR1, hiGIRK2 IUPHAR 435 NCBI...

KCNIP1 KCNIP4 KCNJ10 KCNJ12 KCNJ13 KCNJ14 KCNJ15 KCNJ16 KCNJ3 KCNJ4 KCNJ5 KCNJ6 KCNJ8 KCNJ9 KCNK1 KCNK10 KCNK12 KCNK13 KCNK15 KCNK16 KCNK17 KCNK18 KCNK2...

association study of frontal θ oscillations identifies potassium channel gene KCNJ6". Genes, Brain and Behavior. 11 (6): 712–9. doi:10.1111/j.1601-183X.2012...

heteromultimeric pore-forming complex. KCNJ9 has been shown to interact with KCNJ6. G protein-coupled inwardly-rectifying potassium channel Inward-rectifier...