KCNJ12 - Potassium Inwardly Rectifying Channel Subfamily J Member 12
Alias:
IRK2
hIRK
IRK-2
hIRK1
KCNJN1
Kir2.2
kcnj12x
hkir2.2x
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Description
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Basic Information
Sequence Homology
Related Diseases and Mutations
Transcripts & Proteins
Gene Expression
Interactions
Related Mouse Models
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References Literature
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]