DISEASES

Disease-gene associations mined from literature

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Literature associating CRB1 and Leber congenital amaurosis 8

CRB1 [ENSP00000356370]

Crumbs family member 1, photoreceptor morphogenesis associated; Plays a role in photoreceptor morphogenesis in the retina. May maintain cell polarization and adhesion; Belongs to the Crumbs protein family.

Synonyms:  CRB1,  CRB1p,  hCRB1,  B7Z824,  F5H0L2 ...

Linkouts:  STRING  Pharos  UniProt  OMIM

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.