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KCNJ8

KCNJ8
Identifiers
Aliases KCNJ8, KIR6.1, uKATP-1, potassium voltage-gated channel subfamily J member 8
External IDs MGI: 1100508 HomoloGene: 3654 GeneCards: KCNJ8
Gene location (Human)
Chromosome 12 (human)
Chr. Chromosome 12 (human)
Chromosome 12 (human)
Genomic location for KCNJ8
Genomic location for KCNJ8
Band 12p12.1 Start 21,764,955 bp
End 21,775,581 bp
RNA expression pattern
PBB GE KCNJ8 205303 at fs.png

PBB GE KCNJ8 205304 s at fs.png
More reference expression data
Orthologs
Species Human Mouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_004982

NM_008428
NM_001330363
NM_001330366

RefSeq (protein)

NP_004973

NP_001317292
NP_001317295
NP_032454

Location (UCSC) Chr 12: 21.76 – 21.78 Mb Chr 12: 142.56 – 142.57 Mb
PubMed search

NM_004982

NM_008428
NM_001330363
NM_001330366

NP_004973

NP_001317292
NP_001317295
NP_032454

Potassium inwardly-rectifying channel, subfamily J, member 8, also known as KCNJ8, is a human gene encoding the Kir6.1 protein. A mutation in KCNJ8 has been associated with cardiac arrest in the early repolarization syndrome.

Potassium channels are present in most mammalian cells, where they participate in a wide range of physiologic responses. Kir6.1 is an integral membrane protein and inward-rectifier type potassium channel. Kir6.1, which has a greater tendency to allow potassium to flow into a cell rather than out of a cell, is controlled by G-proteins.

This article incorporates text from the United States National Library of Medicine, which is in the public domain.


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