BRK1
Protein BRICK1
Also known as: BRK1_HUMAN, C3orf10, HSPC300, MDS027
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q8WUW1
- Gene
- BRK1
- Ensembl
- ENSG00000254999
- Chromosome
- 3
- Canonical length
- 75 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Nuclear speckles,Cell Junctions
- Quaternary structure
- Homotrimer
OverviewNCBI Gene
Enables identical protein binding activity. Contributes to small GTPase binding activity. Involved in Rac protein signal transduction and positive regulation of cellular component organization. Located in extracellular exosome. Part of SCAR complex. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
75 residues, UniProt reviewed canonical sequence.
>Q8WUW1|BRK1
1 MAGQEDPVQR EIHQDWANRE YIEIITSSIK KIADFLNSFD MSCRSRLATL NEKLTALERR
61 IEYIEARVTK GETLTLocalizationUniProt · AlphaFold · HPA
Whether an antibody against BRK1 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)
- 0.5
- Highest tissue expression
- 236 nTPM
Expression across tissuesHPA
Tissue
- blood vessel: 236 nTPM
- kidney: 198 nTPM
- colon: 192 nTPM
- urinary bladder: 188 nTPM
- skeletal muscle: 186 nTPM
- esophagus: 185 nTPM
Single-cell type
- late spermatids: 3,909 nCPM
- esophageal apical cells: 1,840 nCPM
- early spermatids: 1,131 nCPM
- esophageal suprabasal cells: 871 nCPM
- megakaryocytes: 569 nCPM
- hofbauer cells: 567 nCPM
Immune cell
- total PBMC: 470 nTPM
- plasmacytoid DC: 406 nTPM
- myeloid DC: 381 nTPM
- eosinophil: 358 nTPM
- non-classical monocyte: 347 nTPM
- neutrophil: 339 nTPM
Brain region
- cerebral cortex: 95 nTPM
- hypothalamus: 94 nTPM
- thalamus: 90 nTPM
- spinal cord: 85 nTPM
- white matter: 84 nTPM
- basal ganglia: 83 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)
- 0.79
- gnomAD pLI
- 0.69
- gnomAD missense Z
- 1.21
- DepMap mean gene effect
- -0.25
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 6% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- actin filament organization
- cell motility
- fibroblast proliferation
- in utero embryonic development
- positive regulation of Arp2/3 complex-mediated actin nucleation
- positive regulation of fibroblast proliferation
- positive regulation of lamellipodium assembly
- positive regulation of protein-containing complex assembly
- Rac protein signal transduction
- regulation of actin polymerization or depolymerization
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Protein BRICK1
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of BRK1 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 BRK1 as an antibody target. Whether an autoantibody or antibody against BRK1 could matter depends on whether native BRK1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
BRK1 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 BRK1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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