Seroatlas · Human Serome Atlas

TMSB10

Thymosin beta-10

Also known as: TB10, TYB10_HUMAN

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

Protein identityUniProt · HPA

UniProt accession
P63313
Gene
TMSB10
Ensembl
ENSG00000034510
Chromosome
2
Canonical length
44 aa
Protein class
Plasma proteins, Predicted intracellular proteins

OverviewNCBI Gene

Predicted to enable actin monomer binding activity. Predicted to be involved in regulation of cell migration. Predicted to be located in cytoskeleton. Predicted to be active in cytoplasm. [provided by Alliance of Genome Resources, Jul 2025]

Canonical amino-acid sequenceUniProt

44 residues, UniProt reviewed canonical sequence.

>P63313|TMSB10
     1  MADKPDMGEI ASFDKAKLKK TETQEKNTLP TKETIEQEKR SEIS

LocalizationUniProt · AlphaFold · HPA

Whether an antibody against TMSB10 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)
0.63
Highest tissue expression
4,897 nTPM

Expression across tissuesHPA

Tissue

  • ovary: 4,897 nTPM
  • thymus: 3,614 nTPM
  • epididymis: 3,365 nTPM
  • lymph node: 3,073 nTPM
  • lung: 2,965 nTPM
  • colon: 2,898 nTPM

Single-cell type

  • extravillous trophoblasts: 17,494 nCPM
  • esophageal apical cells: 13,891 nCPM
  • kupffer cells: 11,216 nCPM
  • epididymal principal cells: 9,412 nCPM
  • esophageal suprabasal cells: 9,192 nCPM
  • enteric transient amplifying cells: 9,113 nCPM

Immune cell

  • total PBMC: 49,899 nTPM
  • T-reg: 24,250 nTPM
  • myeloid DC: 19,881 nTPM
  • classical monocyte: 18,299 nTPM
  • naive B-cell: 16,662 nTPM
  • memory B-cell: 16,260 nTPM

Brain region

  • cerebral cortex: 1,317 nTPM
  • basal ganglia: 1,050 nTPM
  • hypothalamus: 973 nTPM
  • white matter: 917 nTPM
  • thalamus: 889 nTPM
  • amygdala: 832 nTPM

DiseaseUniProt · ClinVar · IEDB · PubMed

Four sources answering four different questions about TMSB10.

Disease | ImmuneIEDB

Conditions an epitope on TMSB10 was assayed in.

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)
1.92
gnomAD pLI
0.02
gnomAD missense Z
0.91
DepMap mean gene effect
-0.45
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

Molecular functions

Cellular components

Protein domainsUniProt · Pfam · InterPro

KeywordsUniProt

InteractionsUniProt · HPA

Protein binding partners of TMSB10 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 TMSB10 as an antibody target. Whether an autoantibody or antibody against TMSB10 could matter depends on whether native TMSB10 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.

TMSB10 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 TMSB10 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.

Canonical record: https://seroatlas.com/gene/TMSB10. 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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