BEND6
BEN domain-containing protein 6
Also known as: bA203B9.1, BEND6_HUMAN, C6orf65, FLJ30162
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q5SZJ8
- Gene
- BEND6
- Ensembl
- ENSG00000151917
- Chromosome
- 6
- Canonical length
- 279 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Plasma membrane
OverviewNCBI Gene
Enables transcription corepressor activity. Predicted to be involved in negative regulation of Notch signaling pathway and positive regulation of neuron differentiation. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
279 residues, UniProt reviewed canonical sequence.
>Q5SZJ8|BEND6
1 MQKIVQTDEI TNTQAFRKGK RKRTETMDSE NANSDMDKGQ RDPYSGNAFL PGESSSEDEE
61 PLAELSKEEL CAKIKSLKEK LTNTRKENSR LRQSLVMLQV LPQAVTQFEE LVGMAEALLK
121 GGGTMSTSAS TLWRATNNSS PDSFASTCSN SNSNSSSPVS LKPEEEHQTD EKQFQIEKWQ
181 IARCNKSKPQ KFINDLMQVL YTNEYMATHS LTGAKSSTSR DKAVKPAMNQ NEVQEIIGVT
241 KQLFPNTDDV SIRRMIGQKL NNCTKKPNLS KNLNSQDIKLocalizationUniProt · AlphaFold · HPA
Whether an antibody against BEND6 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)
- 0.54
- Highest tissue expression
- 45 nTPM
Expression across tissuesHPA
Tissue
- cerebellum: 45 nTPM
- cerebral cortex: 30 nTPM
- amygdala: 18 nTPM
- hippocampal formation: 17 nTPM
- midbrain: 17 nTPM
- basal ganglia: 16 nTPM
Single-cell type
- retinal bipolar cells: 157 nCPM
- brain excitatory neurons: 134 nCPM
- brain inhibitory neurons: 106 nCPM
- retinal amacrine cells: 80 nCPM
- other brain neurons: 78 nCPM
- retinal ganglion cells: 73 nCPM
Immune cell
- plasmacytoid DC: 8.8 nTPM
- myeloid DC: 1.8 nTPM
- NK-cell: 1.5 nTPM
- total PBMC: 0.1 nTPM
- basophil: 0 nTPM
- classical monocyte: 0 nTPM
Brain region
- cerebral cortex: 73 nTPM
- cerebellum: 72 nTPM
- white matter: 54 nTPM
- pons: 52 nTPM
- medulla oblongata: 49 nTPM
- hypothalamus: 43 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)
- 0.98
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.71
- DepMap mean gene effect
- -0.05
- 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
- negative regulation of Notch signaling pathway
- nervous system development
- positive regulation of neuron differentiation
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
- BEN domain
- BEN domain
- BEN domain-containing protein 6-like
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of BEND6 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 BEND6 as an antibody target. Whether an autoantibody or antibody against BEND6 could matter depends on whether native BEND6 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
BEND6 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 BEND6 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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