BSPRY
B box and SPRY domain-containing protein
Also known as: BSPRY_HUMAN, FLJ20150
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q5W0U4
- Gene
- BSPRY
- Ensembl
- ENSG00000119411
- Chromosome
- 9
- Canonical length
- 402 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Cytosol
OverviewNCBI Gene
Predicted to enable ubiquitin protein ligase activity. Predicted to be involved in innate immune response. Predicted to act upstream of or within cellular response to leukemia inhibitory factor. Predicted to be located in cell leading edge; membrane; and perinuclear region of cytoplasm. Predicted to be active in cytoplasm. [provided by Alliance of Genome Resources, Apr 2025]
Canonical amino-acid sequenceUniProt
402 residues, UniProt reviewed canonical sequence.
>Q5W0U4|BSPRY
1 MSAEGAEPGP GSGSGPGPGP LCPEHGQALS WFCGSERRPV CAACAGLGGR CRGHRIRRAE
61 ERAEELRNKI VDQCERLQLQ SAAITKYVAD VLPGKNQRAV SMASAARELV IQRLSLVRSL
121 CESEEQRLLE QVHGEEERAH QSILTQRVHW AEALQKLDTI RTGLVGMLTH LDDLQLIQKE
181 QEIFERTEEA EGILDPQESE MLNFNEKCTR SPLLTQLWAT AVLGSLSGTE DIRIDERTVS
241 PFLQLSDDRK TLTFSTKKSK ACADGPERFD HWPNALAATS FQNGLHAWMV NVQNSCAYKV
301 GVASGHLPRK GSGSDCRLGH NAFSWVFSRY DQEFRFSHNG QHEPLGLLRG PAQLGVVLDL
361 QVQELLFYEP ASGTVLCAHH VSFPGPLFPV FAVADQTISI VRLocalizationUniProt · AlphaFold · HPA
Whether an antibody against BSPRY 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)
- 0.35
- Highest tissue expression
- 421 nTPM
Expression across tissuesHPA
Tissue
- parathyroid gland: 421 nTPM
- salivary gland: 77 nTPM
- pancreas: 39 nTPM
- esophagus: 29 nTPM
- thyroid gland: 28 nTPM
- skin: 25 nTPM
Single-cell type
- esophageal apical cells: 260 nCPM
- breast lactating cells: 174 nCPM
- esophageal suprabasal cells: 155 nCPM
- salivary acinar cells: 152 nCPM
- breast hormone-responsive cells: 86 nCPM
- breast secretory cells: 62 nCPM
Immune cell
- plasmacytoid DC: 4.4 nTPM
- gdT-cell: 0.2 nTPM
- naive CD8 T-cell: 0.1 nTPM
- basophil: 0 nTPM
- classical monocyte: 0 nTPM
- eosinophil: 0 nTPM
Brain region
- basal ganglia: 24 nTPM
- thalamus: 12 nTPM
- cerebellum: 12 nTPM
- midbrain: 10 nTPM
- amygdala: 7.7 nTPM
- cerebral cortex: 7.7 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)
- 1.2
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.13
- DepMap mean gene effect
- 0.06
- DepMap dependency class
- none
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 4% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of BSPRY 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 BSPRY as an antibody target. Whether an autoantibody or antibody against BSPRY could matter depends on whether native BSPRY is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
BSPRY 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 BSPRY as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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