DISEASES

Disease-gene associations mined from literature

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Human genes for glycogen storage disease XV

Glycogen storage disease XV [DOID:0050579]

A glycogen storage disease characterized by muscle weakness and cardiac abnormalities caused and has_material_basis_in mutation in the GYG1 gene that encodes glycogenin-1.

Synonyms:  glycogen storage disease XV,  DOID:0050579,  glycogen storage disease XVs,  glycogen storage disease type XV,  glycogen storage disease type XVs

Linkouts:  OMIM

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.