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

No community annotations yet for SLC35C1.
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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).


Legend

SLC35C1 is highly significantly mutated in
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SLC35C1 is significantly mutated in
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SLC35C1 is near significance in
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Click on a tumor type to see its full list of significant genes.

Data details


• Mutation list for SLC35C1