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KCNJ5

KCNJ5
Identifiers
Aliases KCNJ5, CIR, GIRK4, KATP1, KIR3.4, LQT13, potassium voltage-gated channel subfamily J member 5
External IDs MGI: 104755 HomoloGene: 20248 GeneCards: KCNJ5
Gene location (Human)
Chromosome 11 (human)
Chr. Chromosome 11 (human)
Chromosome 11 (human)
Genomic location for KCNJ5
Genomic location for KCNJ5
Band 11q24.3 Start 128,891,356 bp
End 128,921,035 bp
Orthologs
Species Human Mouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_000890
NM_001354169

NM_010605

RefSeq (protein)

NP_000881
NP_001341098

NP_034735

Location (UCSC) Chr 11: 128.89 – 128.92 Mb Chr 11: 32.31 – 32.34 Mb
PubMed search

NM_000890
NM_001354169

NM_010605

NP_000881
NP_001341098

NP_034735

G protein-activated inward rectifier potassium channel 4 is a protein that in humans is encoded by the KCNJ5 gene and is a type of G protein-gated ion channel.

Potassium channels are present in most mammalian cells, where they participate in a wide range of physiologic responses. The protein encoded by this gene is an integral membrane protein and inward-rectifier type potassium channel. The encoded protein, which has a greater tendency to allow potassium to flow into a cell rather than out of a cell, is controlled by G-proteins. It may associate with other G-protein-activated potassium channel subunits to form a heterotetrameric pore-forming complex.

Mutations in KCNJ5/Kir3.4 cause Andersen-Tawil syndrome .


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