DUSP23
Dual specificity protein phosphatase 23
Also known as: DUS23_HUMAN, DUSP25, FLJ20442
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9BVJ7
- Gene
- DUSP23
- Ensembl
- ENSG00000158716
- Chromosome
- 1
- Canonical length
- 150 aa
- Protein class
- Enzymes, Predicted intracellular proteins
- Subcellular location
- Nucleoplasm
OverviewNCBI Gene
Enables protein tyrosine/serine/threonine phosphatase activity. Involved in dephosphorylation. Located in nucleoplasm. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
150 residues, UniProt reviewed canonical sequence.
>Q9BVJ7|DUSP23
1 MGVQPPNFSW VLPGRLAGLA LPRLPAHYQF LLDLGVRHLV SLTERGPPHS DSCPGLTLHR
61 LRIPDFCPPA PDQIDRFVQI VDEANARGEA VGVHCALGFG RTGTMLACYL VKERGLAAGD
121 AIAEIRRLRP GSIETYEQEK AVFQFYQRTKLocalizationUniProt · AlphaFold · HPA
Whether an antibody against DUSP23 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)
- 0.24
- Highest tissue expression
- 183 nTPM
Expression across tissuesHPA
Tissue
- kidney: 183 nTPM
- liver: 172 nTPM
- salivary gland: 144 nTPM
- adrenal gland: 114 nTPM
- breast: 93 nTPM
- esophagus: 78 nTPM
Single-cell type
- oocytes: 327 nCPM
- submucosal glandular cells: 292 nCPM
- salivary acinar cells: 280 nCPM
- hepatocytes: 261 nCPM
- esophageal suprabasal cells: 257 nCPM
- epididymal efferent duct absorptive cells: 250 nCPM
Immune cell
- myeloid DC: 262 nTPM
- eosinophil: 230 nTPM
- neutrophil: 187 nTPM
- classical monocyte: 182 nTPM
- intermediate monocyte: 154 nTPM
- basophil: 113 nTPM
Brain region
- spinal cord: 25 nTPM
- medulla oblongata: 23 nTPM
- pons: 23 nTPM
- cerebellum: 23 nTPM
- hippocampal formation: 22 nTPM
- hypothalamus: 22 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)
- 1.69
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.3
- DepMap mean gene effect
- 0.12
- DepMap dependency class
- none
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 7% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
Molecular functions
- phosphatase activity
- protein serine/threonine phosphatase activity
- protein tyrosine phosphatase activity
- protein tyrosine/serine/threonine phosphatase activity
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Tyrosine-specific protein phosphatases domain
- Protein-tyrosine phosphatase, catalytic
- Protein-tyrosine phosphatase, active site
- Dual specificity protein phosphatase domain
- Protein-tyrosine phosphatase-like
- Protein Tyrosine Phosphatase
- Swiss Army Knife protein, DSP-PTPase phosphatase domain
- Swiss Army Knife protein, DSP-PTPase phosphatase domain
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads DUSP23 as an antibody target. Whether an autoantibody or antibody against DUSP23 could matter depends on whether native DUSP23 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
DUSP23 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 DUSP23 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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