DISEASES

Disease-gene associations mined from literature

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Literature associating HCCS and linear skin defects with multiple congenital anomalies 2

HCCS [ENSP00000326579]

Holocytochrome c-type synthase; Links covalently the heme group to the apoprotein of cytochrome c.

Synonyms:  HCCS,  A0A024RBY9,  HCCS-001,  HCCS-002,  HCCS-003 ...

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.