DISEASES

Disease-gene associations mined from literature

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Human genes for xeroderma pigmentosum group G

Xeroderma pigmentosum group G [DOID:0110849]

A xeroderma pigmentosum that has_material_basis_in homozygous or compound heterozygous mutation in the ERCC5 gene on chromosome 13q33.

Synonyms:  xeroderma pigmentosum group G,  DOID:0110849,  xeroderma pigmentosum group Gs,  xeroderma pigmentosum VII,  XP7 ...

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.