Kir6.2

Kir6.2 is a major subunit of the ATP-sensitive K+ channel, a lipid-gated inward-rectifier potassium ion channel. The gene encoding the channel is called KCNJ11 and mutations in this gene are associated with congenital hyperinsulinism.

KCNJ11
Identifiers
AliasesKCNJ11, BIR, HHF2, IKATP, KIR6.2, MODY13, PHHI, TNDM3, potassium voltage-gated channel subfamily J member 11, potassium inwardly rectifying channel subfamily J member 11, PNDM2
External IDsOMIM: 600937 MGI: 107501 HomoloGene: 441 GeneCards: KCNJ11
Orthologs
SpeciesHumanMouse
Entrez

3767

16514

Ensembl

ENSG00000187486

ENSMUSG00000096146

UniProt

Q14654

Q61743

RefSeq (mRNA)

NM_000525
NM_001166290
NM_001377296
NM_001377297

NM_001204411
NM_010602

RefSeq (protein)

NP_000516
NP_001159762
NP_001364225
NP_001364226

NP_001191340
NP_034732

Location (UCSC)Chr 11: 17.37 – 17.39 MbChr 7: 45.74 – 45.75 Mb
PubMed search
Wikidata
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