DISEASES

Disease-gene associations mined from literature

SearchDownloadsAbout

Human genes for congenital stationary night blindness 2A

Congenital stationary night blindness 2A [DOID:0110871]

A congenital stationary night blindness that has_material_basis_in mutation in the CACNA1F gene on chromosome Xp11.23.

Synonyms:  congenital stationary night blindness 2A,  DOID:0110871,  congenital stationary night blindness 2A X-linked,  congenital stationary night blindness 2A Xlinked

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.