DPT
Dermatopontin
Also known as: DERM_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q07507
- Gene
- DPT
- Ensembl
- ENSG00000143196
- Chromosome
- 1
- Canonical length
- 201 aa
- Protein class
- Predicted secreted proteins
- Subcellular location
- Vesicles
- Secretome location
- Secreted to extracellular matrix
OverviewNCBI Gene
Dermatopontin is an extracellular matrix protein with possible functions in cell-matrix interactions and matrix assembly. The protein is found in various tissues and many of its tyrosine residues are sulphated. Dermatopontin is postulated to modify the behavior of TGF-beta through interaction with decorin. [provided by RefSeq, Jul 2008]
Canonical amino-acid sequenceUniProt
201 residues, UniProt reviewed canonical sequence.
>Q07507|DPT
1 MDLSLLWVLL PLVTMAWGQY GDYGYPYQQY HDYSDDGWVN LNRQGFSYQC PQGQVIVAVR
61 SIFSKKEGSD RQWNYACMPT PQSLGEPTEC WWEEINRAGM EWYQTCSNNG LVAGFQSRYF
121 ESVLDREWQF YCCRYSKRCP YSCWLTTEYP GHYGEEMDMI SYNYDYYIRG ATTTFSAVER
181 DRQWKFIMCR MTEYDCEFAN VLocalizationUniProt · AlphaFold · HPA
Whether an antibody against DPT 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
- Secreted
- Secreted
- Yes
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.34
- Highest tissue expression
- 431 nTPM
Expression across tissuesHPA
Tissue
- colon: 431 nTPM
- adipose tissue: 314 nTPM
- breast: 251 nTPM
- heart muscle: 243 nTPM
- tongue: 195 nTPM
- vagina: 172 nTPM
Single-cell type
- fibroblasts: 135 nCPM
- leydig cells: 104 nCPM
- peritubular myoid cells: 84 nCPM
- hepatic stellate cells: 71 nCPM
- fibro-adipogenic progenitors: 25 nCPM
- decidual stromal cells: 14 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
- cerebral cortex: 1.5 nTPM
- white matter: 0.8 nTPM
- pons: 0.6 nTPM
- basal ganglia: 0.5 nTPM
- medulla oblongata: 0.5 nTPM
- cerebellum: 0.4 nTPM
DiseaseUniProt · ClinVar · IEDB · PubMed
Four sources answering four different questions about DPT.
Disease | GeneticClinVar
1 pathogenic / likely-pathogenic of 38 ClinVar records.
Conditions with pathogenic or likely-pathogenic variants.
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)
- 1.23
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.08
- DepMap mean gene effect
- 0.07
- DepMap dependency class
- none
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 3% 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
- Dermatopontin
- Dermatopontin
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of DPT 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 DPT as an antibody target. Whether an autoantibody or antibody against DPT could matter depends on whether native DPT is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
DPT is annotated as secreted, so native DPT circulates and is directly accessible to antibodies. Secreted and cell-surface proteins are the autoantibody targets most likely to act like drugs, blocking or depleting the native protein.
Annotation status
The present source text does not explicitly label DPT as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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