GOLGA1

GOLGA1
Identifiers
AliasesGOLGA1, golgin-97, golgin A1
External IDsOMIM: 602502; MGI: 1924149; HomoloGene: 68223; GeneCards: GOLGA1; OMA:GOLGA1 - orthologs
Orthologs
SpeciesHumanMouse
Entrez

2800

76899

Ensembl

ENSG00000136935

ENSMUSG00000026754

UniProt

Q92805

Q9CW79

RefSeq (mRNA)

NM_002077

NM_001290649
NM_029793

RefSeq (protein)

NP_002068

NP_001277578
NP_084069

Location (UCSC)Chr 9: 124.88 – 124.95 MbChr 2: 38.91 – 38.96 Mb
PubMed search
Wikidata
View/Edit HumanView/Edit Mouse

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.