Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
8904
Gene name Gene Name - the full gene name approved by the HGNC.
Copine 1
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
CPNE1
Synonyms (NCBI Gene) Gene synonyms aliases
COPN1, CPN1
Chromosome Chromosome number
20
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
20q11.22
Summary Summary of gene provided in NCBI Entrez Gene.
Calcium-dependent membrane-binding proteins may regulate molecular events at the interface of the cell membrane and cytoplasm. This gene encodes a calcium-dependent protein that also contains two N-terminal type II C2 domains and an integrin A domain-like
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT032109 hsa-let-7d-5p Sequencing 20371350
MIRT043882 hsa-miR-378a-3p CLASH 23622248
MIRT040983 hsa-miR-532-5p CLASH 23622248
MIRT037995 hsa-miR-500a-5p CLASH 23622248
MIRT036389 hsa-miR-1229-3p CLASH 23622248
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0001786 Function Phosphatidylserine binding IDA 9430674
GO:0004175 Function Endopeptidase activity IDA 18212740
GO:0005215 Function Transporter activity TAS 9430674
GO:0005509 Function Calcium ion binding IMP 25450385
GO:0005515 Function Protein binding IPI 12522145, 32296183
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
604205 2314 ENSG00000214078
Protein
UniProt ID Q99829
Protein name Copine-1 (Chromobindin 17) (Copine I)
Protein function Calcium-dependent phospholipid-binding protein that plays a role in calcium-mediated intracellular processes (PubMed:14674885). Involved in the TNF-alpha receptor signaling pathway in a calcium-dependent manner (PubMed:14674885). Exhibits calciu
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00168 C2 6 116 C2 domain Domain
PF00168 C2 138 255 C2 domain Domain
PF07002 Copine 304 521 Copine Family
Tissue specificity TISSUE SPECIFICITY: Expressed in neutrophils (at protein level) (PubMed:12949241). Widely expressed. Expressed in the brain. Expressed in neutrophil precursors from bone marrow and peripheral blood (PubMed:12949241). {ECO:0000269|PubMed:12949241}.
Sequence
Sequence length 537
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  Reactome
    Glycerophospholipid biosynthesis
Neutrophil degranulation
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Schizophrenia SCHIZOPHRENIA 19 rs13447324, rs387906932, rs387906933, rs863223354, rs863223355, rs776061422, rs863223349, rs748809996, rs759748655, rs863223353, rs863223350, rs863223356, rs781821239, rs863223348, rs863223346
View all (12 more)
Associations from Text Mining
Disease Name Relationship Type References
Adenoma Stimulate 18523666
Breast Neoplasms Inhibit 39351539
Carcinogenesis Associate 29207139
Carcinogenesis Stimulate 35101055
Carcinoma Non Small Cell Lung Stimulate 35101055
Dry Eye Syndromes Associate 30312344
Glaucoma Open Angle Stimulate 18523666
Liposarcoma Associate 18820673
Multiple Myeloma Associate 33780365
Neoplasm Metastasis Associate 29207139