GOLGA1

Golgin subfamily A member 1 is a protein that in humans is encoded by the GOLGA1 gene.^[5][6]

GOLGA1
Identifiers
Aliases	GOLGA1, golgin-97, golgin A1
External IDs	OMIM: 602502; MGI: 1924149; HomoloGene: 68223; GeneCards: GOLGA1; OMA:GOLGA1 - orthologs
Gene location (Human) Chr. Chromosome 9 (human)[1] Band 9q33.3 Start 124,878,275 bp[1] End 124,948,492 bp[1]
Gene location (Mouse) Chr. Chromosome 2 (mouse)[2] Band 2|2 B Start 38,906,167 bp[2] End 38,955,553 bp[2]
RNA expression pattern Bgee Human Mouse (ortholog) Top expressed in sural nerve epithelium of colon gonad Achilles tendon testicle right adrenal gland right adrenal cortex stromal cell of endometrium right lobe of liver gastric mucosa Top expressed in otolith organ utricle spermatocyte tail of embryo genital tubercle hand Rostral migratory stream neural layer of retina lacrimal gland cerebellar cortex More reference expression data BioGPS n/a
Orthologs Species Human Mouse 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 Mb Chr 2: 38.91 – 38.96 Mb PubMed search [3] [4]
Wikidata
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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.^[6]

Interactions

GOLGA1 has been shown to interact with ARL1.^[7]