COPRS
Coordinator of PRMT5 and differentiation stimulator
Also known as: C17orf79, COPR5, COPRS_HUMAN, HSA272196, TTP1
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9NQ92
- Gene
- COPRS
- Ensembl
- ENSG00000172301
- Chromosome
- 17
- Canonical length
- 184 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Plasma membrane,Cytosol
OverviewNCBI Gene
Enables histone binding activity. Involved in chromatin remodeling. Located in cytosol; nucleoplasm; and plasma membrane. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
184 residues, UniProt reviewed canonical sequence.
>Q9NQ92|COPRS
1 MDLQAAGAQA QGAAEPSRGP PLPSARGAPP SPEAGFATAD HSSQERETEK AMDRLARGTQ
61 SIPNDSPARG EGTHSEEEGF AMDEEDSDGE LNTWELSEGT NCPPKEQPGD LFNEDWDSEL
121 KADQGNPYDA DDIQESISQE LKPWVCCAPQ GDMIYDPSWH HPPPLIPYYS KMVFETGQFD
181 DAEDLocalizationUniProt · AlphaFold · HPA
Whether an antibody against COPRS 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)
- 0.7
- Highest tissue expression
- 244 nTPM
Expression across tissuesHPA
Tissue
- testis: 244 nTPM
- choroid plexus: 174 nTPM
- cerebral cortex: 146 nTPM
- hypothalamus: 137 nTPM
- amygdala: 125 nTPM
- basal ganglia: 121 nTPM
Single-cell type
- late primary spermatocytes: 982 nCPM
- late spermatids: 422 nCPM
- epididymal efferent duct ciliated cells: 331 nCPM
- fallopian tube ciliated cells: 289 nCPM
- epididymal principal cells: 252 nCPM
- epididymal clear cells: 231 nCPM
Immune cell
- naive B-cell: 3.6 nTPM
- myeloid DC: 2.6 nTPM
- classical monocyte: 2 nTPM
- intermediate monocyte: 2 nTPM
- memory B-cell: 1.9 nTPM
- basophil: 1.8 nTPM
Brain region
- hypothalamus: 81 nTPM
- choroid plexus: 66 nTPM
- basal ganglia: 66 nTPM
- thalamus: 65 nTPM
- pons: 65 nTPM
- cerebral cortex: 63 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)
- 0.83
- gnomAD pLI
- 0.25
- gnomAD missense Z
- 0.02
- DepMap mean gene effect
- -0.2
- DepMap dependency class
- selective
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
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Coordinator of PRMT5 and differentiation stimulator
- Cooperator of PRMT5 family
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of COPRS 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 COPRS as an antibody target. Whether an autoantibody or antibody against COPRS could matter depends on whether native COPRS is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
COPRS 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 COPRS as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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