Brugada syndrome 5

Summary
Synonym
  • BRGDA5
Definition
A Brugada syndrome that has_material_basis_in heterozygous mutation in the SCN1B gene on chromosome 19q13.
Super Class
Brugada syndrome
Disease Ontology
DOID:0110222
Mondo Disease Ontology
MeSH
OMIM
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
6324 SCN1B sodium voltage-gated channel beta subunit 1
Displaying 1 entry
Gene ID Gene Symbol Description Source
20266 Scn1b sodium channel, voltage-gated, type I, beta
Displaying 1 entry
Gene ID Gene Symbol Description Source
29686 Scn1b sodium voltage-gated channel beta subunit 1
The Human Phenotype Ontology
Displaying entries 11 - 12 of 12 in total
HPO ID HPO Term
HP:0001663 Ventricular fibrillation
HP:0004755 Supraventricular tachycardia
Displaying all 2 entries
Gene ID Gene Symbol Description
23171 GPD1L glycerol-3-phosphate dehydrogenase 1 like
781 CACNA2D1 calcium voltage-gated channel auxiliary subunit alpha2delta 1

About Release Notes Help Feedback

Click here to visit the beta site.


International Collaboration

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


Logo License Policies Site Map

Contact: support@glycosmos.org

This work is licensed under Creative Commons Attribution 4.0 International


GlyCosmos Portal v4.1.0

Last updated: December 9, 2024