DISEASES

Disease-gene associations mined from literature

SearchDownloadsAbout

Human genes for Clark-Baraitser syndrome

Clark-Baraitser syndrome [DOID:0080234]

An autosomal dominant intellectual developmental disorder that has_material_basis_in heterozygous mutation in the TRIP12 gene on chromosome 2q36.

Synonyms:  Clark-Baraitser syndrome,  ClarkBaraitser syndrome,  Clark-Baraitser disease,  Clark-Baraitser disorder,  Clark-Baraitser syndromes ...

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.