Gene

KCNJ5

Species
Homo sapiens
Symbol
KCNJ5
Name
potassium inwardly rectifying channel subfamily J member 5
Synonyms
  • cardiac ATP-sensitive potassium channel
  • cardiac inward rectifier
Biotype
protein coding gene
Automated Description
Enables G-protein activated inward rectifier potassium channel activity and voltage-gated potassium channel activity involved in atrial cardiac muscle cell action potential repolarization. Contributes to inward rectifier potassium channel activity. Involved in membrane repolarization during atrial cardiac muscle cell action potential; potassium ion import across plasma membrane; and regulation of heart rate by cardiac conduction. Part of voltage-gated potassium channel complex. Implicated in atrial fibrillation; long QT syndrome 13; and primary hyperaldosteronism.
RGD Description
This gene encodes an integral membrane protein which belongs to one of seven subfamilies of inward-rectifier potassium channel proteins called potassium channel subfamily J. The encoded protein is a subunit of the potassium channel which is homotetrameric. It is controlled by G-proteins and has a greater tendency to allow potassium to flow into a cell rather than out of a cell. Naturally occurring mutations in this gene are associated with aldosterone-producing adenomas. [provided by RefSeq, Aug 2017]
Cross References
Additional Information
Literature

Orthology

Gene tree
PANTHER:PTHR11767
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Paralogy

Function - GO Annotations

Pathways

No data available

Phenotypes

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    Disease Associations

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    Alleles and Variants

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      Transgenic Alleles

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      (carrying the transgene)
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        Models

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          Sequence Feature Viewer

          Genome location
          Assembly version
          GRCh38
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          Sequence Details

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          Expression

          Primary Sources
          None
          Other Sources
          Cell color indicative of annotation volume; red slash indicates species lacks structure or developmental stage.

          Molecular Interactions

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            Genetic Interactions

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