DISEASES

Disease-gene associations mined from literature

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Literature associating SYN3 and hereditary retinal dystrophy

SYN3 [ENSP00000351614]

Synapsin-3; May be involved in the regulation of neurotransmitter release and synaptogenesis.

Synonyms:  SYN3,  SYN3p,  hSYN3,  A0A024R1I8,  A0A087WTG8 ...

Linkouts:  STRING  Pharos  UniProt

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.