DBN1
Drebrin
Also known as: D0S117E, DREB_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q16643
- Gene
- DBN1
- Ensembl
- ENSG00000113758
- Chromosome
- 5
- Canonical length
- 649 aa
- Protein class
- Disease related genes, Plasma proteins, Predicted intracellular proteins
- Subcellular location
- Plasma membrane,Actin filaments
OverviewNCBI Gene
The protein encoded by this gene is a cytoplasmic actin-binding protein thought to play a role in the process of neuronal growth. It is a member of the drebrin family of proteins that are developmentally regulated in the brain. A decrease in the amount of this protein in the brain has been implicated as a possible contributing factor in the pathogenesis of memory disturbance in Alzheimer's disease. At least two alternative splice variants encoding different protein isoforms have been described for this gene. [provided by RefSeq, Jul 2008]
Canonical amino-acid sequenceUniProt
649 residues, UniProt reviewed canonical sequence.
>Q16643|DBN1
1 MAGVSFSGHR LELLAAYEEV IREESAADWA LYTYEDGSDD LKLAASGEGG LQELSGHFEN
61 QKVMYGFCSV KDSQAALPKY VLINWVGEDV PDARKCACAS HVAKVAEFFQ GVDVIVNASS
121 VEDIDAGAIG QRLSNGLARL SSPVLHRLRL REDENAEPVG TTYQKTDAAV EMKRINREQF
181 WEQAKKEEEL RKEEERKKAL DERLRFEQER MEQERQEQEE RERRYREREQ QIEEHRRKQQ
241 TLEAEEAKRR LKEQSIFGDH RDEEEETHMK KSESEVEEAA AIIAQRPDNP REFFKQQERV
301 ASASAGSCDV PSPFNHRPGS HLDSHRRMAP TPIPTRSPSD SSTASTPVAE QIERALDEVT
361 SSQPPPLPPP PPPAQETQEP SPILDSEETR AAAPQAWAGP MEEPPQAQAP PRGPGSPAED
421 LMFMESAEQA VLAAPVEPAT ADATEIHDAA DTIETDTATA DTTVANNVPP AATSLIDLWP
481 GNGEGASTLQ GEPRAPTPPS GTEVTLAEVP LLDEVAPEPL LPAGEGCATL LNFDELPEPP
541 ATFCDPEEVE GESLAAPQTP TLPSALEELE QEQEPEPHLL TNGETTQKEG TQASEGYFSQ
601 SQEEEFAQSE ELCAKAPPPV FYNKPPEIDI TCWDADPVPE EEEGFEGGDLocalizationUniProt · AlphaFold · HPA
Whether an antibody against DBN1 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
- Cell surface
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.59
- Highest tissue expression
- 74 nTPM
Expression across tissuesHPA
Tissue
- endometrium: 74 nTPM
- basal ganglia: 73 nTPM
- cerebral cortex: 66 nTPM
- blood vessel: 63 nTPM
- cervix: 62 nTPM
- hippocampal formation: 59 nTPM
Single-cell type
- decidual stromal cells: 124 nCPM
- platelets: 100 nCPM
- late spermatids: 68 nCPM
- fibroblasts: 60 nCPM
- salivary duct cells: 56 nCPM
- lymphatic endothelial cells: 54 nCPM
Immune cell
- MAIT T-cell: 13 nTPM
- gdT-cell: 9.7 nTPM
- basophil: 9.2 nTPM
- memory CD8 T-cell: 6.9 nTPM
- plasmacytoid DC: 5.3 nTPM
- naive CD8 T-cell: 4.8 nTPM
Brain region
- hippocampal formation: 137 nTPM
- cerebral cortex: 135 nTPM
- basal ganglia: 102 nTPM
- hypothalamus: 89 nTPM
- amygdala: 87 nTPM
- pons: 67 nTPM
DiseaseUniProt · ClinVar · IEDB · PubMed
Four sources answering four different questions about DBN1.
Disease | AllUniProt
Conditions DBN1 is implicated in, by any mechanism.
- Alzheimer disease (AD) MIM:104300
ReferencesPubMed · IEDB
Publications for DBN1 from three distinct lines of evidence, kept separate because they answer different questions: whether antibodies are directed at the protein, whether a B-cell epitope has been mapped on it, and whether a T-cell epitope has. Each is labelled with its source.
Reference: AutoantibodyPubMed
2 publications
- Drebrin Autoantibodies in Patients with Seizures and Suspected Encephalitis.
2020 · Ann Neurol · RCR 1.6 · 29 citations - Adolescent autoimmune encephalitis with dual positive anti-Drebrin and anti-mGluR2 antibodies: a case report.
2026 · Front Immunol
Sources: PubMed — antigen-level antibody evidence from a custom retrieval. Records matching a controlled set of autoantibody terms (the MeSH descriptors Autoantibodies and Autoantigens, with title and abstract term variants) were obtained through NCBI E-utilities, and their titles and abstracts parsed for constructions that direct an antibody at a named protein rather than for co-occurrence. Captured names were resolved against UniProt nomenclature and each antigen adjudicated individually against the source text. Bibliographic records from PubMed and MeSH, U.S. National Library of Medicine; citation metrics from NIH iCite (Hutchins et al., PLoS Biology 2016). Titles link to PubMed; abstracts are not reproduced here. The NLM does not endorse this analysis.
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)
- 0.26
- gnomAD pLI
- 1
- gnomAD missense Z
- 0.67
- DepMap mean gene effect
- -0.07
- 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
- actin filament organization
- cell communication by chemical coupling
- cell communication by electrical coupling
- generation of neurons
- in utero embryonic development
- maintenance of protein location in cell
- neural precursor cell proliferation
- positive regulation of dendritic spine morphogenesis
- positive regulation of receptor localization to synapse
- positive regulation of synaptic plasticity
- regulation of dendrite development
- regulation of neuronal synaptic plasticity
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of DBN1 in the human serome: UniProt-annotated complex subunits plus reported interactors. Each links to its own Seroatlas record.
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads DBN1 as an antibody target. Whether an autoantibody or antibody against DBN1 could matter depends on whether native DBN1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
DBN1 is annotated at the cell surface, where native DBN1 is exposed to circulating antibodies and is a prime autoantibody target that could block, deplete, or overstimulate it.
Annotation status
The present source text does not explicitly label DBN1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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