potassium sodium-activated channel subfamily T member 1

Summary
Gene Symbol
  • KCNT1
Organism
Homo sapiens (human)
NCBI Gene
57582
PubChem
57582
Alliance of Genome Resources
Annotation
Keyword
  • 3D-structure
  • Alternative splicing
  • Calcium
  • Cell membrane
  • Disease variant
  • Epilepsy
  • Glycoprotein
  • Phosphoprotein
  • Potassium channel
  • Proteomics identification
  • Reference proteome
  • Transmembrane helix
Proteins
Displaying all 3 entries
UniProt Protein Name
Q5JUK3
  • KCa4.1
A0A6Q8PGM3
A0A0R4J2E0
Gene Ontology (GO)
GO Hierarchy
GO Hierarchy
OrthoDB (Group)
Group level
Eukaryota
Group Name
potassium channel subfamily t
Functional Category
  • E: Amino acid transport and metabolism
  • K: Transcription
  • T: Signal transduction mechanisms
Disease
Disease Ontology
Displaying all 2 entries
DO ID Disease Name Source
DOID:0060686 autosomal dominant nocturnal frontal lobe epilepsy 5
DOID:0080439 developmental and epileptic encephalopathy 14

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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