GOLGA1
Sign in to saveAlso known as golgin-97, golgin A1
Golgin subfamily A member 1 is a protein that in humans is encoded by the GOLGA1 gene.
Gene data
GOLGA1- Name
- golgin A1
- Type
- protein-coding
- Position
- 124,878,275–124,948,492 (−)
- Aliases
- golgin-97
- Ensembl
- ENSG00000136935
- RefSeq RNA
- NM_002077.4, XM_005251929.5, XM_006717062.5, XM_006717063.5, XM_047423241.1
- RefSeq protein
- NP_002068.2, XP_005251986.1, XP_006717125.1, XP_006717126.1, XP_047279197.1
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. [provided by RefSeq, Feb 2010].
Gene Ontology
Biological process
Molecular function
Pathways
via MyGene.info
Gene · Ensembl
golgin A1
- Symbol
- GOLGA1
- Biotype
- Protein coding
- Organism
- Homo sapiens
- Location
- 9:124,878,275-124,948,492
- Strand
- Reverse (−)
- Assembly
- GRCh38
via Ensembl · EMBL-EBI
Wikidata facts
- Instance of
- gene
- Image
- Protein KIFC3 PDB 2h58.png
Show 8 more facts
- HomoloGene ID
- 68223
- found in taxon
- Homo sapiens
- exact match
- identifiers.org/ncbigene/2800
- genomic end
- 127710771
- genomic start
- 124878275
- chromosome
- human chromosome 9
- cytogenetic location
- 9q33.3
- expressed in
- gastric mucosa
Sources (3)
via Wikidata · CC0
~1 min read
Encyclopedic overview
3 sectionsContents
- Interactions
- References
- Further reading
Golgin subfamily A member 1 is a protein that in humans is encoded by the GOLGA1 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 encoded protein is associated with Sjogren's syndrome.
Excerpted from Wikipedia’s “GOLGA1” article, available under the CC BY-SA 4.0 licence.