DISEASES

Disease-gene associations mined from literature

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Literature associating GPR179 and congenital stationary night blindness

GPR179 [ENSP00000483469]

Probable G-protein coupled receptor 158-like 1; Orphan receptor, involved in vision. Required for signal transduction through retinal depolarizing bipolar cells; Belongs to the G-protein coupled receptor 3 family.

Synonyms:  GPR179,  GPR179p,  hGPR179,  GPR158L,  GPR158L1 ...

Linkouts:  STRING  Pharos

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.