KCNJ6

Protein-coding gene in the species Homo sapiens From Wikipedia, the free encyclopedia

G protein-activated inward rectifier potassium channel 2 is a protein that in humans is encoded by the KCNJ6 gene.[5][6][7] Mutation in KCNJ6 gene has been proposed to be the cause of Keppen-Lubinsky Syndrome (KPLBS).[8]

PDBOrtholog search: PDBe RCSB
AliasesKCNJ6, BIR1, GIRK-2, GIRK2, KATP-2, KATP2, KCNJ7, KIR3.2, hiGIRK2, KPLBS, potassium voltage-gated channel subfamily J member 6, potassium inwardly rectifying channel subfamily J member 6
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KCNJ6
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesKCNJ6, BIR1, GIRK-2, GIRK2, KATP-2, KATP2, KCNJ7, KIR3.2, hiGIRK2, KPLBS, potassium voltage-gated channel subfamily J member 6, potassium inwardly rectifying channel subfamily J member 6
External IDsOMIM: 600877; MGI: 104781; HomoloGene: 1688; GeneCards: KCNJ6; OMA:KCNJ6 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_002240

NM_001025584
NM_001025585
NM_001025590
NM_010606

RefSeq (protein)

NP_002231

NP_001020755
NP_001020756
NP_001020761
NP_034736

Location (UCSC)Chr 21: 37.61 – 38.12 MbChr 16: 94.55 – 94.8 Mb
PubMed search[3][4]
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Function

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 and may be involved in the regulation of insulin secretion by glucose. It associates with two other G-protein-activated potassium channels to form a heteromultimeric pore-forming complex.[7]

Interactions

KCNJ6 has been shown to interact with KCNJ9[9][10] and DLG1.[11]

See also

References

Further reading

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