GOSR1

GOSR1
Identifiers
Aliases	GOSR1, GOLIM2, GOS-28, GOS28, GOS28/P28, GS28, P28, golgi SNAP receptor complex member 1
External IDs	OMIM: 604026; MGI: 1858260; HomoloGene: 37977; GeneCards: GOSR1; OMA:GOSR1 - orthologs
Gene location (Human)
Chr.	Chromosome 17 (human)
End	30,527,592 bp
Gene location (Mouse)
Chr.	Chromosome 11 (mouse)
End	76,654,405 bp
RNA expression pattern
	Top expressed in
	buccal mucosa cell; ; nipple; ; tibia; ; visceral pleura; ; caput epididymis; ; Achilles tendon; ; pancreatic ductal cell; ; parietal pleura; ; corpus epididymis; ; tail of epididymis;
	Top expressed in
	lumbar subsegment of spinal cord; ; stroma of bone marrow; ; left lung lobe; ; granulocyte; ; jejunum; ; epithelium of stomach; ; parotid gland; ; aortic valve; ; seminal vesicula; ; subcutaneous adipose tissue;
	More reference expression data
	n/a
Gene ontology
Molecular function	SNAP receptor activity; SNARE binding;
Cellular component	integral component of membrane; Golgi membrane; cis-Golgi network; Golgi apparatus; SNARE complex; membrane; Golgi medial cisterna; cytosol; transport vesicle;
Biological process	protein transport; endoplasmic reticulum to Golgi vesicle-mediated transport; vesicle fusion; intra-Golgi vesicle-mediated transport; retrograde transport, endosome to Golgi; regulation of vesicle targeting, to, from or within Golgi; vesicle-mediated transport; transport;
	Sources:Amigo / QuickGO
Orthologs
	9527
	53334
	ENSG00000108587
	ENSMUSG00000010392
	O95249
	O88630
	NM_001007024; NM_001007025; NM_004871
	NM_016810; NM_001356321
	NP_001007025; NP_001007026; NP_004862
	NP_058090; NP_001343250
	Wikidata
View/Edit Human	View/Edit Mouse

Golgi SNAP receptor complex member 1 is a protein that in humans is encoded by the GOSR1 gene.

This gene encodes a trafficking membrane protein which transports proteins among the endoplasmic reticulum and the Golgi apparatus and between Golgi compartments. This protein is considered an essential component of the Golgi SNAP receptor (SNARE) complex. Alternatively spliced transcript variants encoding distinct isoforms have been found for this gene.