Lentiviral human KCNJ6 sgRNA gene knockout kit

Human KCNJ6

Gene symbol: KCNJ6
Synonyms: BIR1 GIRK-2 GIRK2 hiGIRK2 KATP-2 KATP2 KCNJ7 KIR3.2 KPLBS
Species: HUMAN
Gene ID: 3763
Summary: 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].
NM numbers targeted (Accession number:Exon:CDS Fragment): NM_002240:3:2