long QT syndrome 6

Summary
Synonym
  • LQT6
Definition
A long QT interval syndrome that has_material_basis_in dominant inheritance of mutation in the KCNE2 gene on chromosome 21q22.11.
Super Class
autosomal dominant disease digenic disease long QT syndrome
External Links
Disease Ontology
DOID:0110648
Mondo Disease Ontology
MeSH
OMIM
GARD
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
9992 KCNE2 potassium voltage-gated channel subfamily E regulatory subunit 2
Displaying 1 entry
Gene ID Gene Symbol Description Source
246133 Kcne2 potassium voltage-gated channel, Isk-related subfamily, gene 2
Displaying 1 entry
Gene ID Gene Symbol Description Source
171138 Kcne2 potassium voltage-gated channel subfamily E regulatory subunit 2

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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