SERPINB12
Serpin B12
Also known as: SPB12_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q96P63
- Gene
- SERPINB12
- Ensembl
- ENSG00000166634
- Chromosome
- 18
- Canonical length
- 405 aa
- Protein class
- Plasma proteins, Predicted intracellular proteins
OverviewNCBI Gene
Enables serine-type endopeptidase inhibitor activity. Predicted to be involved in negative regulation of protein catabolic process. Predicted to act upstream of or within hematopoietic progenitor cell differentiation. Located in collagen-containing extracellular matrix. [provided by Alliance of Genome Resources, Apr 2025]
Canonical amino-acid sequenceUniProt
405 residues, UniProt reviewed canonical sequence.
>Q96P63|SERPINB12
1 MDSLVTANTK FCFDLFQEIG KDDRHKNIFF SPLSLSAALG MVRLGARSDS AHQIDEVLHF
61 NEFSQNESKE PDPCLKSNKQ KAGSLNNESG LVSCYFGQLL SKLDRIKTDY TLSIANRLYG
121 EQEFPICQEY LDGVIQFYHT TIESVDFQKN PEKSRQEINF WVECQSQGKI KELFSKDAIN
181 AETVLVLVNA VYFKAKWETY FDHENTVDAP FCLNANENKS VKMMTQKGLY RIGFIEEVKA
241 QILEMRYTKG KLSMFVLLPS HSKDNLKGLE ELERKITYEK MVAWSSSENM SEESVVLSFP
301 RFTLEDSYDL NSILQDMGIT DIFDETRADL TGISPSPNLY LSKIIHKTFV EVDENGTQAA
361 AATGAVVSER SLRSWVEFNA NHPFLFFIRH NKTQTILFYG RVCSPLocalizationUniProt · AlphaFold · HPA
Whether an antibody against SERPINB12 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)
- 0.23
- Highest tissue expression
- 56 nTPM
Expression across tissuesHPA
Tissue
- skin: 56 nTPM
- vagina: 37 nTPM
- cervix: 24 nTPM
- esophagus: 8.8 nTPM
- thymus: 3.2 nTPM
- breast: 3.1 nTPM
Single-cell type
- esophageal apical cells: 15 nCPM
- suprabasal keratinocytes: 5.2 nCPM
- syncytiotrophoblasts: 3.3 nCPM
- esophageal suprabasal cells: 2 nCPM
- late primary spermatocytes: 1.6 nCPM
- lacrimal acinar cells: 0.9 nCPM
Immune cell
- basophil: 0.2 nTPM
- neutrophil: 0.1 nTPM
- classical monocyte: 0 nTPM
- eosinophil: 0 nTPM
- gdT-cell: 0 nTPM
- intermediate monocyte: 0 nTPM
Brain region
- cerebellum: 2.3 nTPM
- choroid plexus: 1.9 nTPM
- basal ganglia: 1.8 nTPM
- cerebral cortex: 1.8 nTPM
- thalamus: 1.8 nTPM
- white matter: 1.8 nTPM
DiseaseUniProt · ClinVar · IEDB · PubMed
Four sources answering four different questions about SERPINB12.
Disease | ImmuneIEDB
Conditions an epitope on SERPINB12 was assayed in.
- brain glioma T cell
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)
- 1.96
- gnomAD pLI
- 0
- gnomAD missense Z
- -0.71
- DepMap mean gene effect
- 0.13
- DepMap dependency class
- none
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 2% 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 SERPINB12 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 SERPINB12 as an antibody target. Whether an autoantibody or antibody against SERPINB12 could matter depends on whether native SERPINB12 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
SERPINB12 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 SERPINB12 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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