GOLGA1
Template:Short description Template:Cs1 config Template:Infobox gene Golgin subfamily A member 1 is a protein that in humans is encoded by the GOLGA1 gene.[1][2]
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. The golgins are a family of proteins, of which the protein encoded by this gene is a member, that are localized to the Golgi. This encoded protein is associated with Sjogren's syndrome.[2]
Interactions
GOLGA1 has been shown to interact with ARL1.[3]
References
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Further reading
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