All download files including the archive files are now in a publicly accessible Google Storage Bucket. Downloads page links have been updated.

Not found

Our G-nome assistant hasn't been able to find this symbol report. Please check the URL or use our search to find what you are looking for.

Symbol report for KCNJ6

HGNC data for KCNJ6

Approved symbol
KCNJ6
Approved name

potassium inwardly rectifying channel subfamily J member 6

Locus type
gene with protein product
HGNC ID
HGNC:6267
Symbol status
Approved
Previous symbols
KCNJ7
Previous names
potassium inwardly-rectifying channel, subfamily J, member 6
Alias symbols
Kir3.2
GIRK2
KATP2
BIR1
hiGIRK2
Alias names
G protein-activated inward rectifier potassium channel 2
Chromosomal location
21q22.13
UCSC
Alliance of Genome Resources
Bos taurus
KCNJ6 VGNC:53585 VGNC
Canis familiaris
KCNJ6 VGNC:42267 VGNC
Equus caballus
KCNJ6 VGNC:58181 VGNC
Felis catus
KCNJ6 VGNC:67916 VGNC
Macaca mulatta
KCNJ6 VGNC:73991 VGNC
Mus musculus
Kcnj6 MGI:104781 Curated
Pan troglodytes
KCNJ6 VGNC:7466 VGNC
Rattus norvegicus
Kcnj6 RGD:2959
Sus scrofa
KCNJ6 VGNC:89360 VGNC
IUPHAR/BPS Guide to PHARMACOLOGY
435
International Union of Pharmacology. LIV. Nomenclature and molecular relationships of inwardly rectifying potassium channels.
Kubo Y et al. Pharmacol Rev 2005 Dec;57(4)509-526
Kubo Y, Adelman JP, Clapham DE, Jan LY, Karschin A, Kurachi Y, Lazdunski M, Nichols CG, Seino S, Vandenberg CA.
Pharmacol Rev 2005 Dec;57(4)509-526
Characterization and variation of a human inwardly-rectifying-K-channel gene (KCNJ6): a putative ATP-sensitive K-channel subunit.
Sakura H et al. FEBS Lett 1995 Jun;367(2)193-197
Sakura H, Bond C, Warren-Perry M, Horsley S, Kearney L, Tucker S, Adelman J, Turner R, Ashcroft FM.
FEBS Lett 1995 Jun;367(2)193-197
Abstract: The ATP-sensitive K-channel plays a central role in insulin release from pancreatic beta-cells. We report here the cloning of the gene (KCNJ6) encoding a putative subunit of a human ATP-sensitive K-channel expressed in brain and beta-cells, and characterisation of its exon-intron structure. Screening of a somatic cell mapping panel and fluorescent in situ hybridization place the gene on chromosome 21 (21q22.1-22.2). Analysis of single-stranded conformational polymorphisms revealed the presence of two silent polymorphisms (Pro-149: CCG-CCA and Asp-328: GAC-GAT) with similar frequencies in normal and non-insulin-dependent diabetic patients.