DISEASES

Disease-gene associations mined from literature

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Literature associating KHDC1L and facioscapulohumeral muscular dystrophy

KHDC1L [ENSP00000359415]

Putative KHDC1-like protein; KH domain containing 1 like; Belongs to the KHDC1 family.

Synonyms:  KHDC1L,  KHDC1Lp,  hKHDC1L,  Q5JSQ8,  Q5JSQ8p ...

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.