DISEASES

Disease-gene associations mined from literature

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Human genes for achromatopsia 2

Achromatopsia 2 [DOID:0110007]

An achromatopsia that has_material_basis_in homozygous or compound heterozygous mutation in the CNGA3 gene on chromosome 2q11.

Synonyms:  achromatopsia 2,  DOID:0110007,  ACHM2,  RMCH2,  rod monochromacy 2 ...

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.