Gene: KCNJ12 (potassium inwardly-rectifying channel, subfamily J, member 12)  Homo sapiens

Symbol: KCNJ12
Name: potassium inwardly-rectifying channel, subfamily J, member 12
Description: This gene encodes an inwardly rectifying K+ channel which may be blocked by divalent cations. This protein is thought to be one of multiple inwardly rectifying channels which contribute to the cardiac inward rectifier current (IK1). The gene is located within the Smith-Magenis syndrome region on chromosome 17. [provided by RefSeq, Jul 2008]
Type: protein-coding
RefSeq Status: VALIDATED
Also known as: ATP-sensitive inward rectifier potassium channel 12; FLJ14167; hIRK; hIRK1; hkir2.2x; inward rectifier K(+) channel Kir2.2; inward rectifier K(+) channel Kir2.2v; inward rectifier K(+) channel Kir2.6; IRK-2; IRK-2; IRK2; kcnj12x; KCNJ18; KCNJN1; Kir2.2; Kir2.2v; OTTHUMP00000162917; potassium channel, inwardly rectifying subfamily J member 12; potassium channel, inwardly rectifying subfamily J member 18; potassium inwardly-rectifying channel, subfamily J, inhibitor 1
Orthologs: Mus musculus : Kcnj12 (potassium inwardly-rectifying channel, subfamily J, member 12)  MGI
Rattus norvegicus : Kcnj12 (potassium inwardly-rectifying channel, subfamily J, member 12)
Latest Assembly: Human Genome Assembly GRCh37
Position:
MapChrPositionStrandSource
Human Alternate Assembly CHM1_11721,268,947 - 21,312,431+NCBI
Human Genome Assembly HuRef1720,481,596 - 20,525,235+NCBI
Human Genome Assembly GRCh371721,279,699 - 21,323,179+NCBI
Human Genome Assembly Build 361721,220,292 - 21,263,772+NCBI
Human Cytogenetic Map17p11.2 NCBI
Human Genome Assembly1721,259,201 - 21,260,985 NCBI
Model

Launch Genome Browser (GBrowse) : build 36 (hg18) build 37 (hg19)


Gene-Chemical Interaction Annotations
Gene Ontology Annotations
Molecular Pathway Annotations
References - curated
References - uncurated
RGD Disease Portals

Genomics

Comparative Map Data
Position Markers
QTLs in Region (Human Genome Assembly GRCh37)

Sequence

Nucleotide Sequences
Protein Sequences
Promoters

Additional Information

External Database Links
Nomenclature History
 
More on KCNJ12
Entrez Gene
Ensembl Gene
Genome Browser: (hg18) (hg19)
HGNC Report
NCBI Map Viewer
Vista
Vista + UCSC

RGD Object Information
RGD ID: 733298
Created: 2004-01-12
Species: Homo sapiens
Last Modified: 2013-04-09
Status: ACTIVE