Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
83643
Gene name Gene Name - the full gene name approved by the HGNC.
Coiled-coil domain containing 3
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
CCDC3
Synonyms (NCBI Gene) Gene synonyms aliases
-
Chromosome Chromosome number
10
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
10p13
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT022206 hsa-miR-124-3p Microarray 18668037
MIRT868812 hsa-miR-138 CLIP-seq
MIRT868813 hsa-miR-1972 CLIP-seq
MIRT868814 hsa-miR-3179 CLIP-seq
MIRT868815 hsa-miR-3202 CLIP-seq
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0005576 Component Extracellular region IBA 21873635
GO:0005576 Component Extracellular region IDA 28827783
GO:0005783 Component Endoplasmic reticulum IDA
GO:0010629 Process Negative regulation of gene expression IBA 21873635
GO:0010629 Process Negative regulation of gene expression IDA 28827783
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
620579 23813 ENSG00000151468
Protein
UniProt ID Q9BQI4
Protein name Coiled-coil domain-containing protein 3 (Fat/vessel-derived secretory protein) (Favine)
Protein function Negatively regulates TNF-alpha-induced pro-inflammatory response in endothelial cells (ECs) via inhibition of TNF-alpha-induced NF-kappaB activation in ECs (PubMed:25193116). Positively regulates lipid accumulation in adipose cells (By similarit
Family and domains
Tissue specificity TISSUE SPECIFICITY: Expressed in umbilical vein endothelial cells (HUVEC), and at lower levels in aortic smooth muscle cells (HASMC). {ECO:0000269|PubMed:20043878}.
Sequence
MLRQLLLAALCLAGPPAPARACQLPSEWRPLSEGCRAELAETIVYARVLALHPEAPGLYN
HLPWQYHAGQGGLFYSAEVEMLCDQAWGSMLEVPAGSRLNLTGLGYFSCHSHTVVQDYSY
FFFLRMDENYNLLPHGVNFQDAIFPDTQENRRMFSSLFQFSNCSQGQQLATFSSDWEIQE
DSRLMCSSVQKALFEEEDHVKKLQQKVATLEKRNRQLRERVKKVKRSLRQARKKGRHLEL
ANQKLSEKLAAGALPHINARGPVRPPYLRG
Sequence length 270
Interactions View interactions
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Leukemia Leukemia, Myelocytic, Acute rs121909646, rs121913488, rs587776834, rs752746786, rs869312821, rs767454740, rs1554564297 27903959
Unknown
Disease term Disease name Evidence References Source
Oligodendroglioma Oligodendroglioma GWAS
Associations from Text Mining
Disease Name Relationship Type References
Breast Neoplasms Associate 36647876
Diabetic Nephropathies Inhibit 33568476
Uterine Cervical Neoplasms Associate 31081073