VPS25
Vacuolar protein-sorting-associated protein 25
Also known as: DERP9, EAP20, MGC10540, VPS25_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9BRG1
- Gene
- VPS25
- Ensembl
- ENSG00000131475
- Chromosome
- 17
- Canonical length
- 176 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Vesicles
OverviewNCBI Gene
This gene encodes a protein that is a subunit of the endosomal sorting complex required for transport II (ESCRT-II). This protein complex functions in sorting of ubiquitinated membrane proteins during endocytosis. A pseudogene of this gene is present on chromosome 1. [provided by RefSeq, Jul 2013]
Canonical amino-acid sequenceUniProt
176 residues, UniProt reviewed canonical sequence.
>Q9BRG1|VPS25
1 MAMSFEWPWQ YRFPPFFTLQ PNVDTRQKQL AAWCSLVLSF CRLHKQSSMT VMEAQESPLF
61 NNVKLQRKLP VESIQIVLEE LRKKGNLEWL DKSKSSFLIM WRRPEEWGKL IYQWVSRSGQ
121 NNSVFTLYEL TNGEDTEDEE FHGLDEATLL RALQALQQEH KAEIITVSDG RGVKFFLocalizationUniProt · AlphaFold · HPA
Whether an antibody against VPS25 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
- Other membrane
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.3
- Highest tissue expression
- 90 nTPM
Expression across tissuesHPA
Tissue
- esophagus: 90 nTPM
- kidney: 69 nTPM
- parathyroid gland: 68 nTPM
- liver: 67 nTPM
- rectum: 64 nTPM
- epididymis: 62 nTPM
Single-cell type
- esophageal suprabasal cells: 289 nCPM
- esophageal apical cells: 277 nCPM
- extravillous trophoblasts: 240 nCPM
- migrating cytotrophoblasts: 163 nCPM
- cytotrophoblasts: 155 nCPM
- esophageal basal cells: 149 nCPM
Immune cell
- eosinophil: 107 nTPM
- intermediate monocyte: 89 nTPM
- basophil: 86 nTPM
- non-classical monocyte: 83 nTPM
- myeloid DC: 80 nTPM
- NK-cell: 79 nTPM
Brain region
- choroid plexus: 29 nTPM
- cerebellum: 25 nTPM
- thalamus: 24 nTPM
- white matter: 24 nTPM
- medulla oblongata: 23 nTPM
- spinal cord: 23 nTPM
DiseaseUniProt · ClinVar · IEDB · PubMed
Four sources answering four different questions about VPS25.
Disease | GeneticClinVar
1 pathogenic / likely-pathogenic of 23 ClinVar records.
Conditions with pathogenic or likely-pathogenic variants.
- VPS25-related neurodevelopmental delay
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)
- 0.73
- gnomAD pLI
- 0.08
- gnomAD missense Z
- 1.48
- DepMap mean gene effect
- -2.2
- DepMap dependency class
- pan
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
- macroautophagy
- membrane fission
- multivesicular body assembly
- negative regulation of epidermal growth factor-activated receptor activity
- protein transport to vacuole involved in ubiquitin-dependent protein catabolic process via the multivesicular body sorting pathway
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Winged helix-like DNA-binding domain superfamily
- Winged helix DNA-binding domain superfamily
- ESCRT-II complex, Vps25 subunit
- ESCRT-II complex, Vps25 subunit, N-terminal winged helix
- ESCRT-II complex subunit
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of VPS25 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 VPS25 as an antibody target. Whether an autoantibody or antibody against VPS25 could matter depends on whether native VPS25 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
VPS25 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 VPS25 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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