DUSP15
Dual specificity protein phosphatase 15
Also known as: bA243J16.5, bA243J16.6, C20orf57, DUS15_HUMAN, FLJ20645, VHY
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9H1R2
- Gene
- DUSP15
- Ensembl
- ENSG00000149599
- Chromosome
- 20
- Canonical length
- 295 aa
- Protein class
- Enzymes, Predicted intracellular proteins
- Subcellular location
- Plasma membrane,Cytosol
OverviewNCBI Gene
The protein encoded by this gene has both protein-tyrosine phophatase activity and serine/threonine-specific phosphatase activity, and therefore is known as a dual specificity phosphatase. This protein may function in the differentiation of oligodendrocytes. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2016]
Canonical amino-acid sequenceUniProt
295 residues, UniProt reviewed canonical sequence.
>Q9H1R2|DUSP15
1 MTEGVLPGLY LGNFIDAKDL DQLGRNKITH IISIHESPQP LLQDITYLRI PVADTPEVPI
61 KKHFKECINF IHCCRLNGGN CLVHCFAGIS RSTTIVTAYV MTVTGLGWRD VLEAIKATRP
121 IANPNPGFRQ QLEEFGWASS QKGARHRTSK TSGAQCPPMT SATCLLAARV ALLSAALVRE
181 ATGRTAQRCR LSPRAAAERL LGPPPHVAAG WSPDPKYQIC LCFGEEDPGP TQHPKEQLIM
241 ADVQVQLRPG SSSCTLSAST ERPDGSSTPG NPDGITHLQC SCLHPKRAAS SSCTRLocalizationUniProt · AlphaFold · HPA
Whether an antibody against DUSP15 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
- 0
- Mean surface accessibility (rSASA)
- 0.37
- Highest tissue expression
- 209 nTPM
Expression across tissuesHPA
Tissue
- testis: 209 nTPM
- kidney: 49 nTPM
- spinal cord: 19 nTPM
- midbrain: 18 nTPM
- basal ganglia: 13 nTPM
- parathyroid gland: 13 nTPM
Single-cell type
- late spermatids: 1,777 nCPM
- late primary spermatocytes: 365 nCPM
- early spermatids: 277 nCPM
- epididymal principal cells: 65 nCPM
- epididymal clear cells: 51 nCPM
- sertoli cells: 38 nCPM
Immune cell
- naive B-cell: 0.1 nTPM
- basophil: 0 nTPM
- classical monocyte: 0 nTPM
- eosinophil: 0 nTPM
- gdT-cell: 0 nTPM
- intermediate monocyte: 0 nTPM
Brain region
- medulla oblongata: 37 nTPM
- cerebellum: 24 nTPM
- midbrain: 19 nTPM
- white matter: 18 nTPM
- pons: 18 nTPM
- spinal cord: 17 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)
- 1.5
- gnomAD pLI
- 0
- gnomAD missense Z
- -0.4
- DepMap mean gene effect
- 0.09
- DepMap dependency class
- none
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 9% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- dephosphorylation
- negative regulation of transcription by RNA polymerase II
- positive regulation of ERK1 and ERK2 cascade
- regulation of oligodendrocyte differentiation
- signal transduction
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
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads DUSP15 as an antibody target. Whether an autoantibody or antibody against DUSP15 could matter depends on whether native DUSP15 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
DUSP15 is annotated at the cell surface, where native DUSP15 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 DUSP15 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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