DISEASES

Disease-gene associations mined from literature

SearchDownloadsAbout

Human genes for Seckel syndrome 6

Seckel syndrome 6 [DOID:0070006]

A Seckel syndrome that has_material_basis_in homozygous mutation in the CEP63 gene on chromosome 3q22.

Synonyms:  Seckel syndrome 6,  DOID:0070006,  SCKL6

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.