BEX2
Protein BEX2
Also known as: BEX2_HUMAN, DJ79P11.1
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9BXY8
- Gene
- BEX2
- Ensembl
- ENSG00000133134
- Chromosome
- X
- Canonical length
- 128 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Cytosol
OverviewNCBI Gene
This gene belongs to the brain expressed X-linked gene family. The encoded protein interacts with the transcription factor LIM domain only 2 in a DNA-binding complex that recognizes the E-box element and promotes transcription. This gene has been found to be a tumor suppressor that is silenced in human glioma. In breast cancer cells, this gene product modulates apoptosis in response to estrogen and tamoxifen, and enhances the anti-proliferative effect of tamoxifen. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2009]
Canonical amino-acid sequenceUniProt
128 residues, UniProt reviewed canonical sequence.
>Q9BXY8|BEX2
1 MESKEERALN NLIVENVNQE NDEKDEKEQV ANKGEPLALP LNVSEYCVPR GNRRRFRVRQ
61 PILQYRWDIM HRLGEPQARM REENMERIGE EVRQLMEKLR EKQLSHSLRA VSTDPPHHDH
121 HDEFCLMPLocalizationUniProt · AlphaFold · HPA
Whether an antibody against BEX2 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)
- 0.6
- Highest tissue expression
- 301 nTPM
Expression across tissuesHPA
Tissue
- basal ganglia: 301 nTPM
- hypothalamus: 284 nTPM
- cerebral cortex: 277 nTPM
- amygdala: 235 nTPM
- hippocampal formation: 226 nTPM
- cerebellum: 215 nTPM
Single-cell type
- epididymal basal cells: 418 nCPM
- epididymal efferent duct absorptive cells: 320 nCPM
- epididymal principal cells: 239 nCPM
- pancreatic islet cells: 221 nCPM
- müller glia: 203 nCPM
- breast myoepithelial cells: 171 nCPM
Immune cell
- naive CD4 T-cell: 69 nTPM
- NK-cell: 62 nTPM
- memory B-cell: 53 nTPM
- naive CD8 T-cell: 50 nTPM
- memory CD4 T-cell: 44 nTPM
- naive B-cell: 43 nTPM
Brain region
- hypothalamus: 135 nTPM
- cerebral cortex: 121 nTPM
- basal ganglia: 94 nTPM
- white matter: 87 nTPM
- hippocampal formation: 86 nTPM
- midbrain: 77 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)
- 1.27
- gnomAD pLI
- 0.1
- gnomAD missense Z
- -0.01
- DepMap mean gene effect
- 0.01
- 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
- apoptotic process
- negative regulation of protein ubiquitination
- regulation of apoptotic process
- regulation of cell cycle
- signal transduction
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of BEX2 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 BEX2 as an antibody target. Whether an autoantibody or antibody against BEX2 could matter depends on whether native BEX2 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
BEX2 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 BEX2 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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