DCANP1
Dendritic cell nuclear protein 1
Also known as: C5orf20, DCNP1, DCNP1_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q8TF63
- Gene
- DCANP1
- Ensembl
- ENSG00000251380
- Chromosome
- 5
- Canonical length
- 244 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Nuclear bodies
OverviewNCBI Gene
This intronless gene is specifically expressed in dendritic cells (DCs), which are potent antigen-presenting cells involved in activating naive T cells to initiate antigen-specific immune response. The encoded protein is localized mainly in the perinucleus. One of the alleles (A/T) of this gene, that causes premature translation termination at aa 117, has been associated with an increased prevalence of major depression in humans. [provided by RefSeq, Jul 2008]
Canonical amino-acid sequenceUniProt
244 residues, UniProt reviewed canonical sequence.
>Q8TF63|DCANP1
1 MHYGAATHIQ NSRSHGLETV PGHQRLERGA GGETPEFPGC HSPAPPENFG NELLPLSAPL
61 QGLSEGLYPP GRNKTLPAGV LREGAVQFLH RGLCNSNLSS EASARPSGTQ DELHSSRRKT
121 GQTRREGARK HLVCSFRLYP FTVHTVSPGN SHLALYQVFK AVKLCPSETS FFLSRKSLKS
181 SDPWHPPSLS PNSWNRQAGF RAWSSHLISL SLTCSDSQSR RVSSSQQPPL HSLSSHRRAA
241 HVPELocalizationUniProt · AlphaFold · HPA
Whether an antibody against DCANP1 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
- Intracellular
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.7
- Highest tissue expression
- 0.7 nTPM
Expression across tissuesHPA
Tissue
- lymph node: 0.7 nTPM
- spleen: 0.5 nTPM
- skin: 0.4 nTPM
- small intestine: 0.4 nTPM
- tonsil: 0.3 nTPM
- bone marrow: 0.1 nTPM
Single-cell type
- pdcs: 2.5 nCPM
- microglia: 0.8 nCPM
- cdc: 0.3 nCPM
- macrophages: 0.2 nCPM
- monocyte progenitors: 0.1 nCPM
- adipocytes: 0 nCPM
Immune cell
- intermediate monocyte: 0.2 nTPM
- plasmacytoid DC: 0.2 nTPM
- myeloid DC: 0.1 nTPM
- basophil: 0 nTPM
- classical monocyte: 0 nTPM
- eosinophil: 0 nTPM
Brain region
- amygdala: 0 nTPM
- basal ganglia: 0 nTPM
- cerebellum: 0 nTPM
- cerebral cortex: 0 nTPM
- choroid plexus: 0 nTPM
- hippocampal formation: 0 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)
- 0
- gnomAD pLI
- 0
- DepMap mean gene effect
- -0.06
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 3% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- auditory behavior
- cochlea development
- cochlea morphogenesis
- craniofacial suture morphogenesis
- genitalia development
- genitalia morphogenesis
- hard palate morphogenesis
- inner ear development
- inner ear morphogenesis
- learned vocalization behavior
- mastication
- negative regulation of relaxation of muscle
- negative regulation of saliva secretion
- neuromuscular process controlling balance
- peristalsis
- regulation of muscle organ development
- thorax and anterior abdomen determination
- trigeminal nerve development
- vestibulocochlear nerve formation
Molecular functions
Cellular components
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads DCANP1 as an antibody target. Whether an autoantibody or antibody against DCANP1 could matter depends on whether native DCANP1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
DCANP1 is annotated as predominantly intracellular. Intracellular proteins are common autoantibody markers, becoming visible to the immune system after cell injury or altered processing, but are usually markers of disease rather than direct drivers.
Annotation status
The present source text does not explicitly label DCANP1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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