golgi autoantigen, golgin subfamily a, 1

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NCBI Description of GOLGA1

The Golgi apparatus, which participates in glycosylation and transport of proteins and lipids in the secretory pathway, consists of a series of stacked cisternae (flattened membrane sacs). Interactions between the Golgi and microtubules are thought to be important for the reorganization of the Golgi after it fragments during mitosis. This gene encodes one of the golgins, a family of proteins localized to the Golgi. This encoded protein is associated with Sjogren's syndrome.

Community Annotation of GOLGA1 Add / Edit GOLGA1: 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).


GOLGA1 is highly significantly mutated in
GOLGA1 is significantly mutated in
GOLGA1 is near significance in

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

Data details

Mutation list for GOLGA1