SLC35C1 Back

solute carrier family 35, member C1

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NCBI Description of SLC35C1

This gene encodes a GDP-fucose transporter that is found in the Golgi apparatus. Mutations in this gene result in congenital disorder of glycosylation type IIc. Multiple transcript variants encoding different isoforms have been found for this gene.

Community Annotation of SLC35C1 Add / Edit SLC35C1: Annotations

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Figure notes

• "Mouse over" a mutation to see details.
• Missense green saturation indicates evolutionary conservation of the mutated positions.
• Red hashes in protein strip are splice sites.
• Blue-white-red bars are log2 copy ratio distributions (–1 to +1) from Zack et al. (2013).


SLC35C1 is highly significantly mutated in
SLC35C1 is significantly mutated in
SLC35C1 is near significance in

Click on a tumor type to see its full list of significant genes.

Data details

Mutation list for SLC35C1