Kir6.2

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; OMA:KCNJ11 - orthologs
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
View/Edit HumanView/Edit Mouse

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.