DISEASES

Disease-gene associations mined from literature

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Literature associating CCDC50 and chromosome 3q29 microdeletion syndrome

CCDC50 [ENSP00000376250]

Coiled-coil domain-containing protein 50; Involved in EGFR signaling; Deafness associated genes

Synonyms:  CCDC50,  CCDC50p,  hCCDC50,  Q8IVM0,  C3orf6 ...

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.