DISEASES

Disease-gene associations mined from literature

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Human genes for congenital nystagmus 6

Congenital nystagmus 6 [DOID:0111795]

A congenital nystagmus that has_material_basis_in hemizygous of homoxygous mutation in GPR143 on chromosome Xp22.2.

Synonyms:  congenital nystagmus 6,  DOID:0111795,  NYS6,  X-linked congenital nystagmus 6,  Xlinked congenital nystagmus 6

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.