DISEASES

Disease-gene associations mined from literature

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Human genes for Fanconi anemia complementation group T

Fanconi anemia complementation group T [DOID:0111081]

A Fanconi anemia that has_material_basis_in compound heterozygous mutation in the UBE2T gene on chromosome 1q32.

Synonyms:  Fanconi anemia complementation group T,  DOID:0111081,  Fanconi anemia complementation group Ts,  FANCT,  FANCTs

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.