BRD3OS
Uncharacterized protein BRD3OS
Also known as: bA374P20.3, BRDOS_HUMAN, FLJ35348, LINC00094, NCRNA00094, SERLOC
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- A0A1B0GUI7
- Gene
- BRD3OS
- Ensembl
- ENSG00000235106
- Chromosome
- 9
- Canonical length
- 84 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Nucleoli,Vesicles,Cytosol
OverviewNCBI Gene
No narrative summary is available for BRD3OS in this catalog release; identity and structured annotations are shown without generated factual claims.
Canonical amino-acid sequenceUniProt
84 residues, UniProt reviewed canonical sequence.
>A0A1B0GUI7|BRD3OS
1 MSGRVPLAEK ALSEGYARLR YRDTSLLIWQ QQQQKLESVP PGTYLSRSRS MWYSQYGNEA
61 ILVRDKNKLE VSRDTGQSKF CTIMLocalizationUniProt · AlphaFold · HPA
Whether an antibody against BRD3OS 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
- Unknown
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.54
- Highest tissue expression
- 35 nTPM
Expression across tissuesHPA
Tissue
- cerebral cortex: 35 nTPM
- amygdala: 29 nTPM
- retina: 28 nTPM
- basal ganglia: 28 nTPM
- hippocampal formation: 27 nTPM
- pituitary gland: 26 nTPM
Single-cell type
- platelets: 83 nCPM
- late spermatids: 49 nCPM
- respiratory ciliated cells: 47 nCPM
- fallopian tube ciliated cells: 41 nCPM
- late primary spermatocytes: 32 nCPM
- differentiating spermatogonia: 30 nCPM
Immune cell
- naive B-cell: 14 nTPM
- naive CD4 T-cell: 13 nTPM
- memory CD4 T-cell: 13 nTPM
- memory B-cell: 13 nTPM
- gdT-cell: 12 nTPM
- memory CD8 T-cell: 12 nTPM
Brain region
- hippocampal formation: 47 nTPM
- thalamus: 47 nTPM
- cerebral cortex: 45 nTPM
- midbrain: 45 nTPM
- amygdala: 44 nTPM
- basal ganglia: 44 nTPM
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).
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads BRD3OS as an antibody target. Whether an autoantibody or antibody against BRD3OS could matter depends on whether native BRD3OS is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
BRD3OS 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 BRD3OS as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
Loading the interactive Seroatlas protein explorer...