SLC35A1 Back

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

External References:      Wikipedia GeneCards HUGO COSMIC Google Scholar

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

No community annotations yet for SLC35A1.
Sort mutations by: Tumor type  Mutation type  Position  
Straightedge cursor Expand

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

SLC35A1 is highly significantly mutated in
(none)
SLC35A1 is significantly mutated in
(none)
SLC35A1 is near significance in
(none)

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

Data details


• Mutation list for SLC35A1