SPOPL
Speckle-type POZ protein-like
Also known as: BTBD33, SPOPL_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q6IQ16
- Gene
- SPOPL
- Ensembl
- ENSG00000144228
- Chromosome
- 2
- Canonical length
- 392 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Vesicles
- Quaternary structure
- Homodimer
OverviewNCBI Gene
Enables identical protein binding activity. Involved in negative regulation of protein ubiquitination and proteasome-mediated ubiquitin-dependent protein catabolic process. Part of Cul3-RING ubiquitin ligase complex. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
392 residues, UniProt reviewed canonical sequence.
>Q6IQ16|SPOPL
1 MSREPTPPLP GDMSTGPIAE SWCYTQVKVV KFSYMWTINN FSFCREEMGE VLKSSTFSSG
61 PSDKMKWCLR VNPKGLDDES KDYLSLYLLL VSCPKSEVRA KFKFSLLNAK REETKAMESQ
121 RAYRFVQGKD WGFKKFIRRD FLLDEANGLL PDDKLTLFCE VSVVQDSVNI SGHTNTNTLK
181 VPECRLAEDL GNLWENTRFT DCSFFVRGQE FKAHKSVLAA RSPVFNAMFE HEMEESKKNR
241 VEINDLDPEV FKEMMRFIYT GRAPNLDKMA DNLLAAADKY ALERLKVMCE EALCSNLSVE
301 NVADTLVLAD LHSAEQLKAQ AIDFINRCSV LRQLGCKDGK NWNSNQATDI METSGWKSMI
361 QSHPHLVAEA FRALASAQCP QFGIPRKRLK QSLocalizationUniProt · AlphaFold · HPA
Whether an antibody against SPOPL 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)
- 0.34
- Highest tissue expression
- 16 nTPM
Expression across tissuesHPA
Tissue
- blood vessel: 16 nTPM
- bone marrow: 14 nTPM
- breast: 12 nTPM
- salivary gland: 11 nTPM
- lymph node: 11 nTPM
- spleen: 11 nTPM
Single-cell type
- neutrophils: 610 nCPM
- neutrophil progenitors: 298 nCPM
- microglia: 140 nCPM
- breast hormone-responsive cells: 133 nCPM
- monocyte progenitors: 115 nCPM
- renal collecting duct intercalated cells: 114 nCPM
Immune cell
- neutrophil: 5.7 nTPM
- eosinophil: 2.8 nTPM
- myeloid DC: 2.2 nTPM
- classical monocyte: 1.6 nTPM
- intermediate monocyte: 1.5 nTPM
- non-classical monocyte: 1.3 nTPM
Brain region
- midbrain: 19 nTPM
- white matter: 18 nTPM
- basal ganglia: 16 nTPM
- pons: 16 nTPM
- spinal cord: 15 nTPM
- medulla oblongata: 15 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)
- 0.58
- gnomAD pLI
- 0.01
- gnomAD missense Z
- 0.96
- DepMap mean gene effect
- -0.1
- 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 protein ubiquitination
- proteasome-mediated ubiquitin-dependent protein catabolic process
- protein ubiquitination
- regulation of proteolysis
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of SPOPL 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 SPOPL as an antibody target. Whether an autoantibody or antibody against SPOPL could matter depends on whether native SPOPL is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
SPOPL 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 SPOPL as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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