DISEASES

Disease-gene associations mined from literature

SearchDownloadsAbout

Human genes for spinocerebellar ataxia 44

Spinocerebellar ataxia 44 [DOID:0080286]

An autosomal dominant cerebellar ataxia that has_material_basis_in heterozygous mutation in the GRM1 gene on chromosome 6q24.

Synonyms:  spinocerebellar ataxia 44,  DOID:0080286

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.