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Standards Ontologies Notations
long QT syndrome 1

Summary
Synonym
  • LQT1
  • ventricular fibrillation with prolonged QT interval
Definition
A long QT syndrome that has_material_basis_in dominant inheritance of mutation in the KCNQ1 gene on chromosome 11p15.5-p15.4.
Super Class
autosomal dominant disease digenic disease long QT syndrome
Disease Ontology
DOID:0110644
Mondo Disease Ontology
OMIM
GARD
MGI genotype (from TogoID)
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
3784 KCNQ1 potassium voltage-gated channel subfamily Q member 1
Displaying 1 entry
Gene ID Gene Symbol Description Source
16535 Kcnq1 potassium voltage-gated channel, subfamily Q, member 1
Displaying 1 entry
Gene ID Gene Symbol Description Source
84020 Kcnq1 potassium voltage-gated channel subfamily Q member 1
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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