DISEASES

Disease-gene associations mined from literature

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Literature associating SLC35C1 and congenital disorder of glycosylation type IIe

SLC35C1 [ENSP00000313318]

Solute carrier family 35 (GDP-fucose transporter), member C1; Involved in GDP-fucose import from the cytoplasm into the Golgi lumen; Belongs to the TPT transporter family. SLC35C subfamily.

Synonyms:  SLC35C1,  SLC35C1p,  hSLC35C1,  B3KQH0,  E9PPI4 ...

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.