SPSB4
SPRY domain-containing SOCS box protein 4
Also known as: SPSB4_HUMAN, SSB-4
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q96A44
- Gene
- SPSB4
- Ensembl
- ENSG00000175093
- Chromosome
- 3
- Canonical length
- 273 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Golgi apparatus
OverviewNCBI Gene
Enables ubiquitin-like ligase-substrate adaptor activity. Involved in several processes, including positive regulation of protein polyubiquitination; protein ubiquitination; and ubiquitin-dependent protein catabolic process. Located in cytosol. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
273 residues, UniProt reviewed canonical sequence.
>Q96A44|SPSB4
1 MGQKLSGSLK SVEVREPALR PAKRELRGAE PGRPARLDQL LDMPAAGLAV QLRHAWNPED
61 RSLNVFVKDD DRLTFHRHPV AQSTDGIRGK VGHARGLHAW QINWPARQRG THAVVGVATA
121 RAPLHSVGYT ALVGSDAESW GWDLGRSRLY HDGKNQPGVA YPAFLGPDEA FALPDSLLVV
181 LDMDEGTLSF IVDGQYLGVA FRGLKGKKLY PVVSAVWGHC EVTMRYINGL DPEPLPLMDL
241 CRRSIRSALG RQRLQDISSL PLPQSLKNYL QYQLocalizationUniProt · AlphaFold · HPA
Whether an antibody against SPSB4 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)
- 0.29
- Highest tissue expression
- 12 nTPM
Expression across tissuesHPA
Tissue
- pancreas: 12 nTPM
- testis: 6.9 nTPM
- choroid plexus: 4.7 nTPM
- heart muscle: 3.8 nTPM
- pituitary gland: 2.6 nTPM
- spleen: 2.6 nTPM
Single-cell type
- choroid plexus epithelial cells: 83 nCPM
- oligodendrocyte progenitor cells: 76 nCPM
- lactotrophs: 75 nCPM
- kupffer cells: 59 nCPM
- megakaryocytes: 56 nCPM
- gonadotrophs: 51 nCPM
Immune cell
- basophil: 0 nTPM
- classical monocyte: 0 nTPM
- eosinophil: 0 nTPM
- gdT-cell: 0 nTPM
- intermediate monocyte: 0 nTPM
- MAIT T-cell: 0 nTPM
Brain region
- choroid plexus: 7.8 nTPM
- medulla oblongata: 7.2 nTPM
- hypothalamus: 6 nTPM
- midbrain: 5.8 nTPM
- pons: 4.7 nTPM
- spinal cord: 4.2 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)
- 1.41
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.87
- DepMap mean gene effect
- 0.11
- DepMap dependency class
- selective
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
- intracellular signal transduction
- positive regulation of protein polyubiquitination
- proteasome-mediated ubiquitin-dependent protein catabolic process
- protein ubiquitination
- regulation of circadian rhythm
- rhythmic process
- ubiquitin-dependent protein catabolic process
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of SPSB4 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 SPSB4 as an antibody target. Whether an autoantibody or antibody against SPSB4 could matter depends on whether native SPSB4 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
SPSB4 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 SPSB4 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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