TUSC2
Tumor suppressor candidate 2
Also known as: C3orf11, FUS1, PAP, PDAP2, TUSC2_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- O75896
- Gene
- TUSC2
- Ensembl
- ENSG00000114383
- Chromosome
- 3
- Canonical length
- 110 aa
- Protein class
- Cancer-related genes, Predicted intracellular proteins
- Subcellular location
- Vesicles,Cytosol
OverviewNCBI Gene
Predicted to be involved in inflammatory response and regulation of mitochondrial membrane potential. Predicted to act upstream of or within several processes, including natural killer cell differentiation; neutrophil-mediated killing of gram-negative bacterium; and regulation of cytokine production. Predicted to be active in mitochondrion. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
110 residues, UniProt reviewed canonical sequence.
>O75896|TUSC2
1 MGASGSKARG LWPFASAAGG GGSEAAGAEQ ALVRPRGRAV PPFVFTRRGS MFYDEDGDLA
61 HEFYEETIVT KNGQKRAKLR RVHKNLIPQG IVKLDHPRIH VDFPVILYEVLocalizationUniProt · AlphaFold · HPA
Whether an antibody against TUSC2 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)
- 0.57
- Highest tissue expression
- 60 nTPM
Expression across tissuesHPA
Tissue
- cerebral cortex: 60 nTPM
- skeletal muscle: 50 nTPM
- amygdala: 50 nTPM
- basal ganglia: 47 nTPM
- hippocampal formation: 47 nTPM
- hypothalamus: 44 nTPM
Single-cell type
- late spermatids: 584 nCPM
- esophageal suprabasal cells: 161 nCPM
- esophageal apical cells: 140 nCPM
- late primary spermatocytes: 115 nCPM
- early spermatids: 114 nCPM
- oocytes: 101 nCPM
Immune cell
- eosinophil: 35 nTPM
- total PBMC: 32 nTPM
- neutrophil: 30 nTPM
- plasmacytoid DC: 26 nTPM
- memory CD8 T-cell: 25 nTPM
- naive CD8 T-cell: 25 nTPM
Brain region
- midbrain: 49 nTPM
- thalamus: 49 nTPM
- pons: 47 nTPM
- hypothalamus: 47 nTPM
- cerebral cortex: 45 nTPM
- medulla oblongata: 45 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)
- 0.62
- gnomAD pLI
- 0.77
- gnomAD missense Z
- 1.07
- DepMap mean gene effect
- -0.19
- 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
- cell maturation
- inflammatory response
- natural killer cell differentiation
- negative regulation of interleukin-17 production
- neutrophil-mediated killing of gram-negative bacterium
- phagocytosis
- positive regulation of interleukin-10 production
- regulation of mitochondrial membrane potential
- regulation of reactive oxygen species metabolic process
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Tumour suppressor candidate 2
- Tumour suppressor candidate 2
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of TUSC2 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 TUSC2 as an antibody target. Whether an autoantibody or antibody against TUSC2 could matter depends on whether native TUSC2 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
TUSC2 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 TUSC2 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
Loading the interactive Seroatlas protein explorer...