Seroatlas · Human Serome Atlas

TCL1B

T-cell leukemia/lymphoma protein 1B

Also known as: TCL1B_HUMAN, TML1

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

Protein identityUniProt · HPA

UniProt accession
O95988
Gene
TCL1B
Ensembl
ENSG00000213231
Chromosome
14
Canonical length
128 aa
Protein class
Predicted intracellular proteins
Subcellular location
Cytosol

OverviewNCBI Gene

Enables protein kinase binding activity and protein serine/threonine kinase activator activity. Involved in intracellular signal transduction. [provided by Alliance of Genome Resources, Jul 2025]

Canonical amino-acid sequenceUniProt

128 residues, UniProt reviewed canonical sequence.

>O95988|TCL1B
     1  MASEASVRLG VPPGRLWIQR PGIYEDEEGR TWVTVVVRFN PSRREWARAS QGSRYEPSIT
    61  VHLWQMAVHT RELLSSGQMP FSQLPAVWQL YPGRKYRAAD SSFWEIADHG QIDSMEQLVL
   121  TYQPERKD

LocalizationUniProt · AlphaFold · HPA

Whether an antibody against TCL1B 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
Unknown
Secreted
No
Transmembrane segments
0
Mean surface accessibility (rSASA)
0.36
Highest tissue expression
2.5 nTPM

Expression across tissuesHPA

Tissue

  • testis: 2.5 nTPM
  • tonsil: 2.3 nTPM
  • lymph node: 2 nTPM
  • bone marrow: 1.1 nTPM
  • placenta: 0.8 nTPM
  • spleen: 0.7 nTPM

Single-cell type

  • syncytiotrophoblasts: 2.5 nCPM
  • proximal tubule cells: 1.9 nCPM
  • distal convoluted tubule cells: 0.4 nCPM
  • papillary tip epithelial cells: 0.4 nCPM
  • undifferentiated spermatogonia: 0.4 nCPM
  • nk-cells: 0.3 nCPM

Immune cell

  • naive B-cell: 12 nTPM
  • plasmacytoid DC: 6.2 nTPM
  • neutrophil: 0.3 nTPM
  • NK-cell: 0.3 nTPM
  • total PBMC: 0.3 nTPM
  • basophil: 0 nTPM

Brain region

  • white matter: 2.6 nTPM
  • basal ganglia: 2.1 nTPM
  • medulla oblongata: 1.9 nTPM
  • pons: 1.8 nTPM
  • midbrain: 1.5 nTPM
  • thalamus: 1.5 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)
1.24
gnomAD pLI
0.01
gnomAD missense Z
0.21
DepMap mean gene effect
-0.04
DepMap dependency class
selective

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

Protein domainsUniProt · Pfam · InterPro

KeywordsUniProt

InteractionsUniProt · HPA

Protein binding partners of TCL1B 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 TCL1B as an antibody target. Whether an autoantibody or antibody against TCL1B could matter depends on whether native TCL1B is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.

TCL1B 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 TCL1B as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.

Canonical record: https://seroatlas.com/gene/TCL1B. 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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