DISEASES

Disease-gene associations mined from literature

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Human genes for Usher syndrome type 3A

Usher syndrome type 3A [DOID:0110841]

An Usher syndrome type 3 that has_material_basis_in homozygous or compound heterozygous mutation in the CLRN1 gene on chromosome 3q25.

Synonyms:  Usher syndrome type 3A,  DOID:0110841,  USH3A,  Usher syndrome type IIIA,  Usher syndrome type IIIAs

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.