GOLGA4
protein-coding gene in the species Homo sapiens
Golgin subfamily A member 4 is a protein that in humans is encoded by the GOLGA4 gene.
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 protein has been postulated to play a role in Rab6-regulated membrane-tethering events in the Golgi apparatus. Alternative splice variants have been described but their full-length nature has not been determined.
Interactions
GOLGA4 has been shown to interact with ARL1.
Begin with the source’s own compact description: “GOLGA4” is protein-coding gene in the species Homo sapiens. The dossier treats that line as a proposition to test through GOLGA4, protein-coding and gene, not as a finished interpretation.
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Datasets, specimens, observations and peer-reviewed methods provide the appropriate test for the technical claims summarized here. The source revision retrieved here is dated Jul 19, 2025. The linked authority identifier is Q18026299. None of the 0 selected statements returned an explicit reference.
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This entry incorporates text from “GOLGA4” on English Wikipedia. Contributors are listed in the page history. Text is available under the Creative Commons Attribution-ShareAlike 4.0 License. Selected authority identifiers and statements are retrieved from Wikidata under CC0; their references and qualifiers remain part of the verification path.