DISEASES

Disease-gene associations mined from literature

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Human genes for catecholaminergic polymorphic ventricular tachycardia 2

Catecholaminergic polymorphic ventricular tachycardia 2 [DOID:0060676]

A catecholaminergic polymorphic ventricular tachycardia that is characterized by autosomal recessive inheritance and has_material_basis_in homozygous or compound heterozygous mutation in the CASQ2 gene on chromosome 1p13.

Synonyms:  catecholaminergic polymorphic ventricular tachycardia 2,  DOID:0060676,  CVPT2

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.