Gene Gene information from NCBI Gene database.
Entrez ID 55352
Gene name Coordinator of PRMT5 and differentiation stimulator
Gene symbol COPRS
Synonyms (NCBI Gene)
C17orf79COPR5HSA272196TTP1
Chromosome 17
Chromosome location 17q11.2
miRNA miRNA information provided by mirtarbase database.
18
miRTarBase ID miRNA Experiments Reference
MIRT016471 hsa-miR-193b-3p Microarray 20304954
MIRT039412 hsa-miR-421 CLASH 23622248
MIRT447094 hsa-miR-4311 PAR-CLIP 22100165
MIRT447093 hsa-miR-4524b-3p PAR-CLIP 22100165
MIRT447091 hsa-miR-7161-3p PAR-CLIP 22100165
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
15
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 18404153, 33961781
GO:0005634 Component Nucleus IBA
GO:0005634 Component Nucleus IDA 18404153
GO:0005634 Component Nucleus IEA
GO:0005654 Component Nucleoplasm IDA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
HGNC N/A HGNC
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q9NQ92
Protein name Coordinator of PRMT5 and differentiation stimulator (Cooperator of PRMT5) (Protein TTP1)
Protein function Histone-binding protein required for histone H4 methyltransferase activity of PRMT5. Specifically required for histone H4 'Arg-3' methylation mediated by PRMT5, but not histone H3 'Arg-8' methylation, suggesting that it modulates the substrate s
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF15340 COPR5 34 184 Cooperator of PRMT5 family Family
Sequence
Sequence length 184
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  Reactome
    RMTs methylate histone arginines
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
2
Evidence Score: ★☆☆☆☆  Gene-disease association found in Text Mining only ★★☆☆☆  Found in Text Mining and Unknown/Other Associations ★★★☆☆  Reported in Unknown/Other Associations across ≥2 Sources ★★★★☆  ClinVar: Pathogenic/Likely Pathogenic (<5 Variants) ★★★★★  ClinVar: Pathogenic/Likely Pathogenic (≥5 Variants)
Unknown / Other Associations ClinVar entries with uncertain/conflicting evidence, and associations from other databases (OMIM, Orphanet, GWAS, etc.) where the gene is not established as causal.
Phenotype Name Clinical Significance Source Evidence Score
PROSTATE CANCER GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
PROSTATE CARCINOMA GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text Mining Disease associations identified through text mining
Disease Name Disease (Merged) Source PMID Relationship Type Evidence Score
Ataxia with vitamin E deficiency Friedreich Ataxia BEFREE 15065857
★☆☆☆☆
Found in Text Mining only
Intellectual Disability Intellectual developmental disorder Pubtator 11468690 Associate
★☆☆☆☆
Found in Text Mining only
Malignant Peripheral Nerve Sheath Tumor Malignant Peripheral Nerve Sheath Tumor BEFREE 20844836
★☆☆☆☆
Found in Text Mining only
Neurofibrosarcoma Neurofibrosarcoma Pubtator 20844836 Stimulate
★☆☆☆☆
Found in Text Mining only