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Kir6.2

KCNJ11
Identifiers
Aliases KCNJ11, BIR, HHF2, IKATP, KIR6.2, MODY13, PHHI, TNDM3, potassium voltage-gated channel subfamily J member 11
External IDs OMIM: 600937 MGI: 107501 HomoloGene: 441 GeneCards: KCNJ11
Genetically Related Diseases
type 2 diabetes mellitus
Targeted by Drug
minoxidil, nicorandil, glyburide, tolbutamide
Orthologs
Species Human Mouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_000525
NM_001166290

NM_001204411
NM_010602

RefSeq (protein)

NP_000516
NP_001159762

NP_034732.1
NP_001191340
NP_034732

Location (UCSC) Chr 11: 17.39 – 17.39 Mb Chr 7: 46.09 – 46.1 Mb
PubMed search

NM_000525
NM_001166290

NM_001204411
NM_010602

NP_000516
NP_001159762

NP_034732.1
NP_001191340
NP_034732

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


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