Seroatlas · Human Serome Atlas

TSPO2

Translocator protein 2

Also known as: BZRPL1, dJ34B21.2, TSPO2_HUMAN

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

Protein identityUniProt · HPA

UniProt accession
Q5TGU0
Gene
TSPO2
Ensembl
ENSG00000112212
Chromosome
6
Canonical length
170 aa
Protein class
Predicted intracellular proteins, Predicted membrane proteins, Transporters
Subcellular location
Plasma membrane
Quaternary structure
Homotetramer

OverviewNCBI Gene

Enables 5-aminolevulinic acid transmembrane transporter activity. Involved in 5-aminolevulinic acid import across plasma membrane. Located in organelle membrane and plasma membrane. [provided by Alliance of Genome Resources, Jul 2025]

Canonical amino-acid sequenceUniProt

170 residues, UniProt reviewed canonical sequence.

>Q5TGU0|TSPO2
     1  MRLQGAIFVL LPHLGPILVW LFTRDHMSGW CEGPRMLSWC PFYKVLLLVQ TAIYSVVGYA
    61  SYLVWKDLGG GLGWPLALPL GLYAVQLTIS WTVLVLFFTV HNPGLALLHL LLLYGLVVST
   121  ALIWHPINKL AALLLLPYLA WLTVTSALTY HLWRDSLCPV HQPQPTEKSD

LocalizationUniProt · AlphaFold · HPA

Whether an antibody against TSPO2 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
Cell surface
Secreted
No
Transmembrane segments
5
Mean surface accessibility (rSASA)
0.36
Highest tissue expression
47 nTPM

Expression across tissuesHPA

Tissue

  • bone marrow: 47 nTPM
  • spleen: 1.2 nTPM
  • duodenum: 1.1 nTPM
  • placenta: 1.1 nTPM
  • small intestine: 0.7 nTPM
  • gallbladder: 0.6 nTPM

Single-cell type

  • erythrocytes: 62 nCPM
  • erythrocyte progenitors: 32 nCPM
  • cholangiocytes: 2 nCPM
  • enterocytes: 1.8 nCPM
  • foveolar cells: 1.5 nCPM
  • neuroendocrine cells: 0.8 nCPM

Immune cell

  • basophil: 0 nTPM
  • classical monocyte: 0 nTPM
  • eosinophil: 0 nTPM
  • gdT-cell: 0 nTPM
  • intermediate monocyte: 0 nTPM
  • MAIT T-cell: 0 nTPM

Brain region

  • white matter: 5.4 nTPM
  • medulla oblongata: 4.2 nTPM
  • cerebral cortex: 4 nTPM
  • basal ganglia: 3.6 nTPM
  • pons: 3.6 nTPM
  • thalamus: 3.6 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)
1.61
gnomAD pLI
0
gnomAD missense Z
0.55
DepMap mean gene effect
0.07
DepMap dependency class
none

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

Antibody and autoantibody relevanceSeroatlas analysis

Seroatlas reads TSPO2 as an antibody target. Whether an autoantibody or antibody against TSPO2 could matter depends on whether native TSPO2 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.

TSPO2 is annotated at the cell surface, where native TSPO2 is exposed to circulating antibodies and is a prime autoantibody target that could block, deplete, or overstimulate it.

Annotation status

The present source text does not explicitly label TSPO2 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.

Canonical record: https://seroatlas.com/gene/TSPO2. 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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