long QT syndrome 3

Summary
Synonym
  • LQT3
Definition
A long QT syndrome that has_material_basis_in dominant inheritance of mutation in the SCN5A gene on chromosome 3p22.2.
Super Class
autosomal dominant disease digenic disease long QT syndrome
External Links
Disease Ontology
DOID:0110646
Mondo Disease Ontology
MeSH
OMIM
GARD
MGI genotype (from TogoID)
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
6331 SCN5A sodium voltage-gated channel alpha subunit 5
Displaying 1 entry
Gene ID Gene Symbol Description Source
20271 Scn5a sodium channel, voltage-gated, type V, alpha
Displaying 1 entry
Gene ID Gene Symbol Description Source
25665 Scn5a sodium voltage-gated channel alpha subunit 5
Displaying 1 entry
Gene ID Gene Symbol Description Source
32619 para paralytic

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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: August 19, 2024