COPZ1
Coatomer subunit zeta-1
Also known as: CGI-120, COPZ, COPZ1_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- P61923
- Gene
- COPZ1
- Ensembl
- ENSG00000111481
- Chromosome
- 12
- Canonical length
- 177 aa
- Protein class
- Predicted intracellular proteins
OverviewNCBI Gene
This gene encodes a subunit of the cytoplasmic coatamer protein complex, which is involved in autophagy and intracellular protein trafficking. The coatomer protein complex is comprised of seven subunits and functions as the coat protein of coat protein complex (COP)I-vesicles. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2012]
Canonical amino-acid sequenceUniProt
177 residues, UniProt reviewed canonical sequence.
>P61923|COPZ1
1 MEALILEPSL YTVKAILILD NDGDRLFAKY YDDTYPSVKE QKAFEKNIFN KTHRTDSEIA
61 LLEGLTVVYK SSIDLYFYVI GSSYENELML MAVLNCLFDS LSQMLRKNVE KRALLENMEG
121 LFLAVDEIVD GGVILESDPQ QVVHRVALRG EDVPLTEQTV SQVLQSAKEQ IKWSLLRLocalizationUniProt · AlphaFold · HPA
Whether an antibody against COPZ1 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)
- 0.32
- Highest tissue expression
- 142 nTPM
Expression across tissuesHPA
Tissue
- pancreas: 142 nTPM
- epididymis: 118 nTPM
- choroid plexus: 112 nTPM
- thyroid gland: 108 nTPM
- liver: 107 nTPM
- kidney: 106 nTPM
Single-cell type
- esophageal apical cells: 545 nCPM
- extravillous trophoblasts: 353 nCPM
- esophageal suprabasal cells: 311 nCPM
- migrating cytotrophoblasts: 254 nCPM
- syncytiotrophoblasts: 227 nCPM
- hofbauer cells: 207 nCPM
Immune cell
- plasmacytoid DC: 152 nTPM
- non-classical monocyte: 135 nTPM
- total PBMC: 135 nTPM
- myeloid DC: 128 nTPM
- classical monocyte: 128 nTPM
- intermediate monocyte: 118 nTPM
Brain region
- choroid plexus: 77 nTPM
- white matter: 54 nTPM
- thalamus: 51 nTPM
- hypothalamus: 50 nTPM
- basal ganglia: 49 nTPM
- midbrain: 48 nTPM
DiseaseUniProt · ClinVar · IEDB · PubMed
Four sources answering four different questions about COPZ1.
Disease | GeneticClinVar
1 pathogenic / likely-pathogenic of 38 ClinVar records.
Conditions with pathogenic or likely-pathogenic variants.
- Neutropenia, severe congenital, 12, autosomal recessive
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)
- 0.34
- gnomAD pLI
- 0.95
- gnomAD missense Z
- 0.77
- DepMap mean gene effect
- -1.44
- DepMap dependency class
- pan
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
- intra-Golgi vesicle-mediated transport
- intracellular protein transport
- retrograde vesicle-mediated transport, Golgi to endoplasmic reticulum
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of COPZ1 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 COPZ1 as an antibody target. Whether an autoantibody or antibody against COPZ1 could matter depends on whether native COPZ1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
COPZ1 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 COPZ1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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