DISEASES

Disease-gene associations mined from literature

SearchDownloadsAbout

Human genes for retinitis pigmentosa 11

Retinitis pigmentosa 11 [DOID:0110408]

A retinitis pigmentosa that has_material_basis_in mutation in the PRPF31 gene on chromosome 19q13.

Synonyms:  retinitis pigmentosa 11,  DOID:0110408,  RP11

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.