GOLGA8A

Protein-coding gene in the species Homo sapiens From Wikipedia, the free encyclopedia

Golgin A8 family member A is a protein that in humans is encoded by the GOLGA8A gene.[3]

AliasesGOLGA8A, GM88, golgin A8 family member A, GOLGA8B, CFAP286, FAP286
End34,437,808 bp[1]
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GOLGA8A
Identifiers
AliasesGOLGA8A, GM88, golgin A8 family member A, GOLGA8B, CFAP286, FAP286
External IDsOMIM: 616180; HomoloGene: 121673; GeneCards: GOLGA8A; OMA:GOLGA8A - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

n/a

RefSeq (protein)

NP_851422
NP_001355000
NP_001355001

n/a

Location (UCSC)Chr 15: 34.38 – 34.44 Mbn/a
PubMed search[2]n/a
Wikidata
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Function

The Golgi apparatus, which participates in glycosylation and transport of proteins and lipids in the secretory pathway, consists of a series of stacked, flattened membrane sacs referred to as cisternae. Interactions between the Golgi and microtubules are thought to be important for the reorganization of the Golgi after it fragments during mitosis. The golgins constitute a family of proteins which are localized to the Golgi. This gene encodes a golgin which structurally resembles its family member GOLGA2, suggesting that they may share a similar function. There are many similar copies of this gene on chromosome 15. Alternative splicing results in multiple transcript variants.

References

Further reading

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