DISEASES

Disease-gene associations mined from literature

SearchDownloadsAbout

Human genes for Brugada syndrome 1

Brugada syndrome 1 [DOID:0110218]

A Brugada syndrome that has_material_basis_in heterozygous mutation in the SCN5A gene on chromosome 3p22.

Synonyms:  Brugada syndrome 1,  DOID:0110218,  BRGDA1

The disease-gene associations are derived from automatic text mining of the biomedical literature, manually curated database annotations, cancer mutation data, and genome-wide association studies. The confidence of each association is signified by stars, where ★★★★★ is the highest confidence and ★☆☆☆☆ is the lowest.

Developed by Sune Frankild, Alexander Junge, Albert Pallejà, Dhouha Grissa, Kalliopi Tsafou, and Lars Juhl Jensen from the Novo Nordisk Foundation Center for Protein Research.