KCNJ12

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

ATP-sensitive inward rectifier potassium channel 12 is a lipid-gated ion channel that in humans is encoded by the KCNJ12 gene.[5][6][7][8][9]

AliasesKCNJ12, IRK-2, IRK2, KCNJN1, Kir2.2, Kir2.2v, hIRK, hIRK1, hkir2.2x, kcnj12x, potassium voltage-gated channel subfamily J member 12, potassium inwardly rectifying channel subfamily J member 12
End21,419,870 bp[1]
Quick facts Identifiers, Aliases ...
KCNJ12
Identifiers
AliasesKCNJ12, IRK-2, IRK2, KCNJN1, Kir2.2, Kir2.2v, hIRK, hIRK1, hkir2.2x, kcnj12x, potassium voltage-gated channel subfamily J member 12, potassium inwardly rectifying channel subfamily J member 12
External IDsOMIM: 602323; MGI: 108495; HomoloGene: 7793; GeneCards: KCNJ12; OMA:KCNJ12 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_021012

NM_001267593
NM_010603

RefSeq (protein)

NP_066292

NP_001254522
NP_034733

Location (UCSC)Chr 17: 21.38 – 21.42 MbChr 11: 60.91 – 60.96 Mb
PubMed search[3][4]
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Function

This gene encodes an inwardly rectifying K+ channel that may be blocked by divalent cations. This protein is thought to be one of multiple inwardly rectifying channels that contribute to the cardiac inward rectifier current (IK1). The gene is located within the Smith–Magenis syndrome region on chromosome 17.[9]

Interactions

KCNJ12 has been shown to interact with:

See also

References

Further reading

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