potassium voltage-gated channel subfamily Q member 1

Summary
Gene Symbol
  • KCNQ1
Organism
Homo sapiens (human)
External Links
NCBI Gene
3784
PubChem
3784
Alliance of Genome Resources
Annotation
Keyword
  • 3D-structure
  • Alternative splicing
  • Atrial fibrillation
  • Calmodulin-binding
  • Cell membrane
  • Coiled coil
  • Cytoplasmic vesicle
  • Deafness
  • Diabetes mellitus
  • Disease variant
  • Endoplasmic reticulum
  • Endosome
  • Glycoprotein
  • Long QT syndrome
  • Phosphoprotein
  • Potassium channel
  • Reference proteome
  • Short QT syndrome
  • Transmembrane helix
  • Ubl conjugation
  • Voltage-gated channel
Proteins
Displaying all 2 entries
UniProt Protein Name
Q96AI9
P51787
  • IKs producing slow voltage-gated potassium channel subunit alpha KvLQT1
  • KQT-like 1
  • Voltage-gated potassium channel subunit Kv7.1
Gene Ontology (GO)
GO Hierarchy
GO Hierarchy
GO Hierarchy
Disease
Disease Ontology
Displaying all 9 entries
DO ID Disease Name Source
DOID:0050650 familial atrial fibrillation
DOID:0050793 short QT syndrome
DOID:0060224 atrial fibrillation
DOID:0110644 long QT syndrome 1
DOID:10763 hypertension
DOID:2842 Jervell-Lange Nielsen syndrome
DOID:2843 long QT syndrome
DOID:4440 seminoma
DOID:9352 type 2 diabetes mellitus

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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: August 19, 2024