GOSR1
Golgi SNAP receptor complex member 1
Also known as: GOLIM2, GOS-28, GOS28, GOSR1_HUMAN, GS28, P28
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- O95249
- Gene
- GOSR1
- Ensembl
- ENSG00000108587
- Chromosome
- 17
- Canonical length
- 250 aa
- Protein class
- Predicted membrane proteins
OverviewNCBI Gene
This gene encodes a trafficking membrane protein which transports proteins among the endoplasmic reticulum and the Golgi 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. [provided by RefSeq, Jul 2008]
Canonical amino-acid sequenceUniProt
250 residues, UniProt reviewed canonical sequence.
>O95249|GOSR1
1 MAAGTSSYWE DLRKQARQLE NELDLKLVSF SKLCTSYSHS STRDGRRDRY SSDTTPLLNG
61 SSQDRMFETM AIEIEQLLAR LTGVNDKMAE YTNSAGVPSL NAALMHTLQR HRDILQDYTH
121 EFHKTKANFM AIRERENLMG SVRKDIESYK SGSGVNNRRT ELFLKEHDHL RNSDRLIEET
181 ISIAMATKEN MTSQRGMLKS IHSKMNTLAN RFPAVNSLIQ RINLRKRRDS LILGGVIGIC
241 TILLLLYAFHLocalizationUniProt · AlphaFold · HPA
Whether an antibody against GOSR1 can act on the native protein depends on physical access: surface and secreted proteins are reachable by circulating antibodies, intracellular proteins usually are not.
- Antibody reachability
- Other membrane
- Secreted
- No
- Transmembrane segments
- 1
- Mean surface accessibility (rSASA)
- 0.42
- Highest tissue expression
- 29 nTPM
Expression across tissuesHPA
Tissue
- liver: 29 nTPM
- parathyroid gland: 27 nTPM
- kidney: 23 nTPM
- tonsil: 23 nTPM
- thyroid gland: 23 nTPM
- thymus: 23 nTPM
Single-cell type
- late primary spermatocytes: 165 nCPM
- myonuclei: 132 nCPM
- somatotrophs: 130 nCPM
- lactotrophs: 128 nCPM
- adrenal medulla cells: 117 nCPM
- corticotrophs: 112 nCPM
Immune cell
- NK-cell: 36 nTPM
- naive B-cell: 36 nTPM
- MAIT T-cell: 35 nTPM
- memory B-cell: 34 nTPM
- naive CD4 T-cell: 34 nTPM
- T-reg: 34 nTPM
Brain region
- cerebellum: 31 nTPM
- midbrain: 30 nTPM
- thalamus: 29 nTPM
- choroid plexus: 29 nTPM
- cerebral cortex: 29 nTPM
- medulla oblongata: 29 nTPM
Genetic constraint and essentialitygnomAD · DepMap
Does the body need this protein intact? Low LOEUF or a strong DepMap dependency means loss or blockade of the protein is likely to be felt.
- gnomAD LOEUF (loss-of-function intolerance)
- 0.64
- gnomAD pLI
- 0.06
- gnomAD missense Z
- 0.52
- DepMap mean gene effect
- -0.19
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 7% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- endoplasmic reticulum to Golgi vesicle-mediated transport
- inter-Golgi cisterna vesicle-mediated transport
- intra-Golgi vesicle-mediated transport
- protein transport
- retrograde transport, endosome to Golgi
- vesicle fusion
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Snare region anchored in the vesicle membrane C-terminus
- Golgi SNAP receptor complex, subunit 1
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of GOSR1 in the human serome: UniProt-annotated complex subunits plus reported interactors. Each links to its own Seroatlas record.
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads GOSR1 as an antibody target. Whether an autoantibody or antibody against GOSR1 could matter depends on whether native GOSR1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
GOSR1 is annotated as predominantly intracellular. Intracellular proteins are common autoantibody markers, becoming visible to the immune system after cell injury or altered processing, but are usually markers of disease rather than direct drivers.
Annotation status
The present source text does not explicitly label GOSR1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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