Seroatlas · Human Serome Atlas

DUSP19

Dual specificity protein phosphatase 19

Also known as: DUS19_HUMAN, DUSP17, SKRP1

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

Protein identityUniProt · HPA

UniProt accession
Q8WTR2
Gene
DUSP19
Ensembl
ENSG00000162999
Chromosome
2
Canonical length
217 aa
Protein class
Enzymes, Predicted intracellular proteins
Subcellular location
Nucleoplasm

OverviewNCBI Gene

Dual-specificity phosphatases (DUSPs) constitute a large heterogeneous subgroup of the type I cysteine-based protein-tyrosine phosphatase superfamily. DUSPs are characterized by their ability to dephosphorylate both tyrosine and serine/threonine residues. They have been implicated as major modulators of critical signaling pathways. DUSP19 contains a variation of the consensus DUSP C-terminal catalytic domain, with the last serine residue replaced by alanine, and lacks the N-terminal CH2 domain found in the MKP (mitogen-activated protein kinase phosphatase) class of DUSPs (see MIM 600714) (summary by Patterson et al., 2009 [PubMed 19228121]).[supplied by OMIM, Dec 2009]

Canonical amino-acid sequenceUniProt

217 residues, UniProt reviewed canonical sequence.

>Q8WTR2|DUSP19
     1  MYSLNQEIKA FSRNNLRKQC TRVTTLTGKK IIETWKDARI HVVEEVEPSS GGGCGYVQDL
    61  SSDLQVGVIK PWLLLGSQDA AHDLDTLKKN KVTHILNVAY GVENAFLSDF TYKSISILDL
   121  PETNILSYFP ECFEFIEEAK RKDGVVLVHC NAGVSRAAAI VIGFLMNSEQ TSFTSAFSLV
   181  KNARPSICPN SGFMEQLRTY QEGKESNKCD RIQENSS

LocalizationUniProt · AlphaFold · HPA

Whether an antibody against DUSP19 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)
0.35
Highest tissue expression
3.7 nTPM

Expression across tissuesHPA

Tissue

  • stomach: 3.7 nTPM
  • testis: 3.4 nTPM
  • epididymis: 3.3 nTPM
  • fallopian tube: 3 nTPM
  • heart muscle: 2.9 nTPM
  • blood vessel: 2.4 nTPM

Single-cell type

  • parietal cells: 110 nCPM
  • late primary spermatocytes: 32 nCPM
  • fallopian tube ciliated cells: 29 nCPM
  • respiratory ciliated cells: 27 nCPM
  • megakaryocytes: 25 nCPM
  • endometrial ciliated cells: 20 nCPM

Immune cell

  • memory B-cell: 1.1 nTPM
  • T-reg: 1 nTPM
  • memory CD8 T-cell: 0.8 nTPM
  • basophil: 0.7 nTPM
  • naive CD4 T-cell: 0.7 nTPM
  • naive CD8 T-cell: 0.7 nTPM

Brain region

  • hippocampal formation: 13 nTPM
  • cerebral cortex: 11 nTPM
  • basal ganglia: 10 nTPM
  • amygdala: 8 nTPM
  • white matter: 5.9 nTPM
  • hypothalamus: 5.3 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
-0.09
DepMap mean gene effect
0
DepMap dependency class
selective

Cancer expressionTCGA

Across TCGA tumor cohorts, this protein is over-expressed in roughly 5% 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 DUSP19 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 DUSP19 as an antibody target. Whether an autoantibody or antibody against DUSP19 could matter depends on whether native DUSP19 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.

DUSP19 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 DUSP19 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.

Canonical record: https://seroatlas.com/gene/DUSP19. 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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