TRAPPC3
Trafficking protein particle complex subunit 3
Also known as: BET3, TPPC3_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- O43617
- Gene
- TRAPPC3
- Ensembl
- ENSG00000054116
- Chromosome
- 1
- Canonical length
- 180 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Golgi apparatus,Cytosol
- Quaternary structure
- Homodimer
OverviewNCBI Gene
This gene encodes a component of the trafficking protein particle complex, which tethers transport vesicles to the cis-Golgi membrane. The encoded protein participates in the regulation of transport from the endoplasmic reticulum to the Golgi apparatus. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2012]
Canonical amino-acid sequenceUniProt
180 residues, UniProt reviewed canonical sequence.
>O43617|TRAPPC3
1 MSRQANRGTE SKKMSSELFT LTYGALVTQL CKDYENDEDV NKQLDKMGFN IGVRLIEDFL
61 ARSNVGRCHD FRETADVIAK VAFKMYLGIT PSITNWSPAG DEFSLILENN PLVDFVELPD
121 NHSSLIYSNL LCGVLRGALE MVQMAVEAKF VQDTLKGDGV TEIRMRFIRR IEDNLPAGEELocalizationUniProt · AlphaFold · HPA
Whether an antibody against TRAPPC3 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
- Intracellular
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.33
- Highest tissue expression
- 84 nTPM
Expression across tissuesHPA
Tissue
- choroid plexus: 84 nTPM
- adrenal gland: 69 nTPM
- esophagus: 58 nTPM
- epididymis: 57 nTPM
- thyroid gland: 56 nTPM
- colon: 52 nTPM
Single-cell type
- esophageal apical cells: 476 nCPM
- late primary spermatocytes: 385 nCPM
- esophageal suprabasal cells: 265 nCPM
- early spermatids: 260 nCPM
- syncytiotrophoblasts: 238 nCPM
- extravillous trophoblasts: 177 nCPM
Immune cell
- basophil: 163 nTPM
- total PBMC: 155 nTPM
- eosinophil: 149 nTPM
- intermediate monocyte: 143 nTPM
- T-reg: 136 nTPM
- neutrophil: 135 nTPM
Brain region
- choroid plexus: 53 nTPM
- white matter: 43 nTPM
- medulla oblongata: 42 nTPM
- spinal cord: 41 nTPM
- cerebellum: 39 nTPM
- hypothalamus: 37 nTPM
DiseaseUniProt · ClinVar · IEDB · PubMed
Four sources answering four different questions about TRAPPC3.
Disease | GeneticClinVar
1 pathogenic / likely-pathogenic of 54 ClinVar records.
Conditions with pathogenic or likely-pathogenic variants.
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)
- 0.84
- gnomAD pLI
- 0.25
- gnomAD missense Z
- 1.2
- DepMap mean gene effect
- -1.58
- DepMap dependency class
- pan
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 6% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- COPII vesicle coating
- endoplasmic reticulum to Golgi vesicle-mediated transport
- intra-Golgi vesicle-mediated transport
- vesicle coating
- vesicle tethering
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of TRAPPC3 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 TRAPPC3 as an antibody target. Whether an autoantibody or antibody against TRAPPC3 could matter depends on whether native TRAPPC3 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
TRAPPC3 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 TRAPPC3 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
Loading the interactive Seroatlas protein explorer...