DISEASES

Disease-gene associations mined from literature

SearchDownloadsAbout

Human genes for retinitis pigmentosa 32

Retinitis pigmentosa 32 [DOID:0110355]

A retinitis pigmentosa that has_material_basis_in variation in the chromosome region 1p21.3-p13.3.

Synonyms:  retinitis pigmentosa 32,  DOID:0110355,  RP32

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.