potassium voltage-gated channel subfamily Q member 2

Summary
Gene Symbol
  • KCNQ2
Organism
Homo sapiens (human)
NCBI Gene
3785
PubChem
3785
Alliance of Genome Resources
Annotation
Keyword
  • 3D-structure
  • Alternative splicing
  • Cell membrane
  • Disease variant
  • Epilepsy
  • Intellectual disability
  • Phosphoprotein
  • Potassium channel
  • Reference proteome
  • Transmembrane helix
  • Ubl conjugation
  • Voltage-gated channel
Proteins
Displaying all 2 entries
UniProt Protein Name
Q53Y30
O43526
  • KQT-like 2
  • Neuroblastoma-specific potassium channel subunit alpha KvLQT2
  • Voltage-gated potassium channel subunit Kv7.2
Gene Ontology (GO)
GO Hierarchy
GO Hierarchy
OrthoDB (Group)
Group level
Eukaryota
Group Name
Potassium voltage-gated channel subfamily KQT member
Functional Category
  • E: Amino acid transport and metabolism
  • K: Transcription
  • P: Inorganic ion transport and metabolism
  • T: Signal transduction mechanisms
Disease
Disease Ontology
Displaying all 5 entries
DO ID Disease Name Source
DOID:0080462 developmental and epileptic encephalopathy 7
DOID:0112202 developmental and epileptic encephalopathy
DOID:10273 heart conduction disease
DOID:14264 benign neonatal seizures
DOID:2843 long QT syndrome

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GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

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


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Last updated: December 9, 2024