SLC35A1 Back

solute carrier family 35 (CMP-sialic acid transporter), member A1

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NCBI Description of SLC35A1

The protein encoded by this gene is found in the membrane of the Golgi apparatus, where it transports nucleotide sugars into the Golgi. One such nucleotide sugar is CMP-sialic acid, which is imported into the Golgi by the encoded protein and subsequently glycosylated. Defects in this gene are a cause of congenital disorder of glycosylation type 2F (CDG2F). Two transcript variants encoding different isoforms have been found for this gene.

Community Annotation of SLC35A1 Add / Edit SLC35A1: 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).


SLC35A1 is highly significantly mutated in
SLC35A1 is significantly mutated in
SLC35A1 is near significance in

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

Data details

Mutation list for SLC35A1