Gene Gene information from NCBI Gene database.
Entrez ID 27132
Gene name Copine 7
Gene symbol CPNE7
Synonyms (NCBI Gene)
-
Chromosome 16
Chromosome location 16q24.3
Summary This gene encodes a member of the copine family, which is composed of calcium-dependent membrane-binding proteins. The gene product contains two N-terminal C2 domains and one von Willebrand factor A domain. The encoded protein may be involved in membrane
miRNA miRNA information provided by mirtarbase database.
29
miRTarBase ID miRNA Experiments Reference
MIRT024962 hsa-miR-214-3p Microarray;Other 19859982
MIRT906744 hsa-miR-1207-5p CLIP-seq
MIRT906745 hsa-miR-24 CLIP-seq
MIRT906746 hsa-miR-3622b-5p CLIP-seq
MIRT906747 hsa-miR-3918 CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
18
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 25416956, 32296183
GO:0005544 Function Calcium-dependent phospholipid binding IBA
GO:0005544 Function Calcium-dependent phospholipid binding IEA
GO:0005634 Component Nucleus IDA 21087455
GO:0005634 Component Nucleus IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
605689 2320 ENSG00000178773
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q9UBL6
Protein name Copine-7 (Copine VII)
Protein function Calcium-dependent phospholipid-binding protein that may play a role in calcium-mediated intracellular processes.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00168 C2 26 129 C2 domain Domain
PF00168 C2 234 340 C2 domain Domain
PF07002 Copine 401 618 Copine Family
Tissue specificity TISSUE SPECIFICITY: Expressed in the brain, testis, thymus and small intestine (PubMed:10534407, PubMed:12949241). {ECO:0000269|PubMed:10534407, ECO:0000269|PubMed:12949241}.
Sequence
Sequence length 633
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  Reactome
    Glycerophospholipid biosynthesis
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
1
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Gastric cancer Uncertain significance rs145462508 RCV005932276
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
Colorectal Neoplasms Stimulate 38069026
Multiple Myeloma Associate 33780365
Neoplasm Metastasis Associate 38069026