CCDC3
Coiled-coil domain-containing protein 3
Also known as: CCDC3_HUMAN, DKFZp761F241
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9BQI4
- Gene
- CCDC3
- Ensembl
- ENSG00000151468
- Chromosome
- 10
- Canonical length
- 270 aa
- Protein class
- Predicted intracellular proteins, Predicted secreted proteins
- Subcellular location
- Nucleoplasm,Cytosol
- Secretome location
- Secreted to blood
- Quaternary structure
- Homodimer
OverviewNCBI Gene
Involved in negative regulation of lipid metabolic process; negative regulation of tumor necrosis factor-mediated signaling pathway; and signal transduction. Located in endoplasmic reticulum and extracellular region. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
270 residues, UniProt reviewed canonical sequence.
>Q9BQI4|CCDC3
1 MLRQLLLAAL CLAGPPAPAR ACQLPSEWRP LSEGCRAELA ETIVYARVLA LHPEAPGLYN
61 HLPWQYHAGQ GGLFYSAEVE MLCDQAWGSM LEVPAGSRLN LTGLGYFSCH SHTVVQDYSY
121 FFFLRMDENY NLLPHGVNFQ DAIFPDTQEN RRMFSSLFQF SNCSQGQQLA TFSSDWEIQE
181 DSRLMCSSVQ KALFEEEDHV KKLQQKVATL EKRNRQLRER VKKVKRSLRQ ARKKGRHLEL
241 ANQKLSEKLA AGALPHINAR GPVRPPYLRGLocalizationUniProt · AlphaFold · HPA
Whether an antibody against CCDC3 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
- Secreted
- Secreted
- Yes
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.43
- Highest tissue expression
- 310 nTPM
Expression across tissuesHPA
Tissue
- blood vessel: 310 nTPM
- skin: 125 nTPM
- adipose tissue: 86 nTPM
- ovary: 79 nTPM
- gallbladder: 66 nTPM
- fallopian tube: 63 nTPM
Single-cell type
- medullary thymic epithelial cells: 367 nCPM
- vascular smooth muscle cells: 331 nCPM
- adipocytes: 282 nCPM
- pericytes: 135 nCPM
- brain excitatory neurons: 109 nCPM
- oocytes: 106 nCPM
Immune cell
- gdT-cell: 0.1 nTPM
- total PBMC: 0.1 nTPM
- basophil: 0 nTPM
- classical monocyte: 0 nTPM
- eosinophil: 0 nTPM
- intermediate monocyte: 0 nTPM
Brain region
- cerebral cortex: 52 nTPM
- hippocampal formation: 43 nTPM
- amygdala: 37 nTPM
- basal ganglia: 36 nTPM
- white matter: 34 nTPM
- hypothalamus: 13 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)
- 1.09
- gnomAD pLI
- 0
- gnomAD missense Z
- -0.85
- DepMap mean gene effect
- 0.08
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 5% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- lipid biosynthetic process
- negative regulation of gene expression
- negative regulation of lipid biosynthetic process
- negative regulation of lipid metabolic process
- negative regulation of tumor necrosis factor-mediated signaling pathway
- positive regulation of fat cell differentiation
- positive regulation of lipid biosynthetic process
- signal transduction
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Coiled-coil domain-containing protein 3
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads CCDC3 as an antibody target. Whether an autoantibody or antibody against CCDC3 could matter depends on whether native CCDC3 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
CCDC3 is annotated as secreted, so native CCDC3 circulates and is directly accessible to antibodies. Secreted and cell-surface proteins are the autoantibody targets most likely to act like drugs, blocking or depleting the native protein.
Annotation status
The present source text does not explicitly label CCDC3 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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