potassium inwardly rectifying channel subfamily J member 5

Summary
Gene Symbol
  • KCNJ5
Organism
Homo sapiens (human)
NCBI Gene
3762
PubChem
3762
Alliance of Genome Resources
Annotation
Keyword
  • Disease variant
  • Long QT syndrome
  • Phosphoprotein
  • Potassium transport
  • Reference proteome
  • Transmembrane helix
  • Voltage-gated channel
Proteins
Displaying all 2 entries
UniProt Protein Name
A0A5J6E2W8
  • Cardiac inward rectifier
  • Heart KATP channel
  • Inward rectifier K(+) channel Kir3.4
  • KATP-1
  • Potassium channel, inwardly rectifying subfamily J member 5
P48544
  • Cardiac inward rectifier
  • Heart KATP channel
  • Inward rectifier K(+) channel Kir3.4
  • KATP-1
  • Potassium channel, inwardly rectifying subfamily J member 5
Gene Ontology (GO)
GO Hierarchy
GO Hierarchy
OrthoDB (Group)
Disease
Disease Ontology
Displaying all 3 entries
DO ID Disease Name Source
DOID:0060224 atrial fibrillation
DOID:0110654 long QT syndrome 13
DOID:446 primary hyperaldosteronism

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: December 8, 2025