Seroatlas · Human Serome Atlas

S100B

Protein S100-B

Also known as: S100B_HUMAN, S100beta

Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene

Protein identityUniProt · HPA

UniProt accession
P04271
Gene
S100B
Ensembl
ENSG00000160307
Chromosome
21
Canonical length
92 aa
Protein class
Cancer-related genes, Candidate cardiovascular disease genes, Predicted intracellular proteins, Transporters
Subcellular location
Nucleoplasm,Vesicles,Microtubules,Primary cilium,Basal body,Cytosol
Secretome location
Secreted - unknown location

OverviewNCBI Gene

The protein encoded by this gene is a member of the S100 family of proteins containing 2 EF-hand calcium-binding motifs. S100 proteins are localized in the cytoplasm and/or nucleus of a wide range of cells, and involved in the regulation of a number of cellular processes such as cell cycle progression and differentiation. S100 genes include at least 13 members which are located as a cluster on chromosome 1q21; however, this gene is located at 21q22.3. This protein may function in Neurite extension, proliferation of melanoma cells, stimulation of Ca2+ fluxes, inhibition of PKC-mediated phosphorylation, astrocytosis and axonal proliferation, and inhibition of microtubule assembly. Chromosomal rearrangements and altered expression of this gene have been implicated in several neurological, neoplastic, and other types of diseases, including Alzheimer's disease, Down's syndrome, epilepsy, amyotrophic lateral sclerosis, melanoma, and type I diabetes. [provided by RefSeq, Jul 2008]

Canonical amino-acid sequenceUniProt

92 residues, UniProt reviewed canonical sequence.

>P04271|S100B
     1  MSELEKAMVA LIDVFHQYSG REGDKHKLKK SELKELINNE LSHFLEEIKE QEVVDKVMET
    61  LDNDGDGECD FQEFMAFVAM VTTACHEFFE HE

LocalizationUniProt · AlphaFold · HPA

Whether an antibody against S100B 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
Secreted
Secreted
Yes
Transmembrane segments
0
Mean surface accessibility (rSASA)
0.35
Highest tissue expression
4,757 nTPM

Expression across tissuesHPA

Tissue

  • spinal cord: 4,757 nTPM
  • midbrain: 2,119 nTPM
  • hippocampal formation: 945 nTPM
  • hypothalamus: 902 nTPM
  • amygdala: 794 nTPM
  • basal ganglia: 711 nTPM

Single-cell type

  • schwann cells: 1,449 nCPM
  • bergmann glia: 671 nCPM
  • oligodendrocytes: 513 nCPM
  • retinal pigment epithelial cells: 307 nCPM
  • astrocytes: 256 nCPM
  • melanocytes: 211 nCPM

Immune cell

  • gdT-cell: 362 nTPM
  • naive CD8 T-cell: 154 nTPM
  • MAIT T-cell: 104 nTPM
  • memory CD8 T-cell: 68 nTPM
  • total PBMC: 64 nTPM
  • NK-cell: 59 nTPM

Brain region

  • medulla oblongata: 1,735 nTPM
  • white matter: 1,695 nTPM
  • cerebellum: 1,235 nTPM
  • pons: 1,086 nTPM
  • spinal cord: 1,057 nTPM
  • basal ganglia: 827 nTPM

DiseaseUniProt · ClinVar · IEDB · PubMed

Four sources answering four different questions about S100B.

Disease | ImmuneIEDB

Conditions an epitope on S100B was assayed in.

Disease | AutoantibodyPubMed

Conditions in which antibodies against S100B are reported. Each links to that disease's full target list.

ReferencesPubMed · IEDB

Publications for S100B from three distinct lines of evidence, kept separate because they answer different questions: whether antibodies are directed at the protein, whether a B-cell epitope has been mapped on it, and whether a T-cell epitope has. Each is labelled with its source.

Reference: AutoantibodyPubMed

17 publications

Show 12 more

Sources: PubMed — antigen-level antibody evidence from a custom retrieval. Records matching a controlled set of autoantibody terms (the MeSH descriptors Autoantibodies and Autoantigens, with title and abstract term variants) were obtained through NCBI E-utilities, and their titles and abstracts parsed for constructions that direct an antibody at a named protein rather than for co-occurrence. Captured names were resolved against UniProt nomenclature and each antigen adjudicated individually against the source text. IEDB — curated epitope assays from the Immune Epitope Database (Vita et al., Nucleic Acids Research 2019). Bibliographic records from PubMed and MeSH, U.S. National Library of Medicine; citation metrics from NIH iCite (Hutchins et al., PLoS Biology 2016). Titles link to PubMed; abstracts are not reproduced here. The NLM does not endorse this analysis.

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)
1.73
gnomAD pLI
0.04
gnomAD missense Z
0.4
DepMap mean gene effect
0.18
DepMap dependency class
none

Cancer expressionTCGA

Across TCGA tumor cohorts, this protein is over-expressed in roughly 3% 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 S100B 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 S100B as an antibody target. Whether an autoantibody or antibody against S100B could matter depends on whether native S100B is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.

S100B is annotated as secreted, so native S100B circulates and is directly accessible to antibodies. Secreted and cell-surface proteins are the autoantibody targets most likely to act like drugs, blocking or depleting the native protein.

Annotation status

The present source text does not explicitly label S100B as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.

Canonical record: https://seroatlas.com/gene/S100B. Study-independent annotations aggregated from UniProt, Human Protein Atlas, PubMed, IEDB, Pfam, InterPro, Gene Ontology, AlphaFold, gnomAD, DepMap, ClinVar, TCGA. Catalog release seroatlas-reviewed-human-uniprot-20260313.

Seroatlas is the reference for exploring autoantibody and antibody serology at the human-protein level: the autoreactome and human serome, multiplex serology (HuProt, HuScan, VirScan, PhIP-Seq).

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