potassium inwardly rectifying channel subfamily J member 1

Summary
Gene Symbol
  • KCNJ1
Organism
Homo sapiens (human)
NCBI Gene
3758
PubChem
3758
Alliance of Genome Resources
Annotation
Keyword
  • ATP-binding
  • Alternative splicing
  • Bartter syndrome
  • Cell membrane
  • Disease variant
  • Glycoprotein
  • Phosphoprotein
  • Potassium transport
  • Reference proteome
  • Transmembrane helix
  • Voltage-gated channel
Proteins
Displaying all 2 entries
UniProt Protein Name
A8K432
P48048
  • ATP-regulated potassium channel ROM-K
  • Inward rectifier K(+) channel Kir1.1
  • Potassium channel, inwardly rectifying subfamily J member 1
Gene Ontology (GO)
GO Hierarchy
GO Hierarchy
Disease
Disease Ontology
Displaying 1 entry
DO ID Disease Name Source
DOID:0110143 Bartter disease type 2

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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: April 7, 2025