SAR1A
Small COPII coat GTPase SAR1A
Also known as: SAR1, SAR1A_HUMAN, Sara, SARA1
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9NR31
- Gene
- SAR1A
- Ensembl
- ENSG00000079332
- Chromosome
- 10
- Canonical length
- 198 aa
- Protein class
- Plasma proteins, Predicted intracellular proteins
- Subcellular location
- Endoplasmic reticulum
- Quaternary structure
- Homodimer
OverviewNCBI Gene
Enables G protein activity and amino acid sensor activity. Involved in COPII-coated vesicle budding; cellular response to leucine starvation; and negative regulation of TORC1 signaling. Is active in COPII vesicle coat; endoplasmic reticulum exit site; and lysosomal membrane. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
198 residues, UniProt reviewed canonical sequence.
>Q9NR31|SAR1A
1 MSFIFEWIYN GFSSVLQFLG LYKKSGKLVF LGLDNAGKTT LLHMLKDDRL GQHVPTLHPT
61 SEELTIAGMT FTTFDLGGHE QARRVWKNYL PAINGIVFLV DCADHSRLVE SKVELNALMT
121 DETISNVPIL ILGNKIDRTD AISEEKLREI FGLYGQTTGK GNVTLKELNA RPMEVFMCSV
181 LKRQGYGEGF RWLSQYIDLocalizationUniProt · AlphaFold · HPA
Whether an antibody against SAR1A 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
- 0
- Mean surface accessibility (rSASA)
- 0.27
- Highest tissue expression
- 154 nTPM
Expression across tissuesHPA
Tissue
- bone marrow: 154 nTPM
- adipose tissue: 72 nTPM
- placenta: 71 nTPM
- liver: 66 nTPM
- tongue: 53 nTPM
- choroid plexus: 52 nTPM
Single-cell type
- esophageal apical cells: 356 nCPM
- syncytiotrophoblasts: 309 nCPM
- extravillous trophoblasts: 261 nCPM
- breast lactating cells: 213 nCPM
- suprabasal keratinocytes: 212 nCPM
- gastric progenitor cells: 208 nCPM
Immune cell
- NK-cell: 104 nTPM
- total PBMC: 96 nTPM
- MAIT T-cell: 95 nTPM
- naive CD8 T-cell: 89 nTPM
- gdT-cell: 88 nTPM
- memory CD8 T-cell: 86 nTPM
Brain region
- choroid plexus: 86 nTPM
- white matter: 81 nTPM
- thalamus: 78 nTPM
- hypothalamus: 77 nTPM
- spinal cord: 75 nTPM
- midbrain: 70 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)
- 0.7
- gnomAD pLI
- 0.37
- gnomAD missense Z
- 2.09
- DepMap mean gene effect
- -0.16
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 5% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- cellular response to leucine starvation
- COPII vesicle coating
- COPII-coated vesicle cargo loading
- endoplasmic reticulum to Golgi vesicle-mediated transport
- intracellular protein transport
- membrane organization
- negative regulation of TORC1 signaling
- regulation of COPII vesicle coating
- regulation of TORC1 signaling
- vesicle organization
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of SAR1A 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 SAR1A as an antibody target. Whether an autoantibody or antibody against SAR1A could matter depends on whether native SAR1A is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
SAR1A 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 SAR1A as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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