VAMP4
Vesicle-associated membrane protein 4
Also known as: VAMP4_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- O75379
- Gene
- VAMP4
- Ensembl
- ENSG00000117533
- Chromosome
- 1
- Canonical length
- 141 aa
- Protein class
- Predicted membrane proteins
- Subcellular location
- Golgi apparatus
OverviewNCBI Gene
Synaptobrevins/VAMPs, syntaxins, and the 25-kD synaptosomal-associated protein SNAP25 are the main components of a protein complex involved in the docking and/or fusion of synaptic vesicles with the presynaptic membrane. The protein encoded by this gene is a member of the vesicle-associated membrane protein (VAMP)/synaptobrevin family. This protein may play a role in trans-Golgi network-to-endosome transport. [provided by RefSeq, Jul 2008]
Canonical amino-acid sequenceUniProt
141 residues, UniProt reviewed canonical sequence.
>O75379|VAMP4
1 MPPKFKRHLN DDDVTGSVKS ERRNLLEDDS DEEEDFFLRG PSGPRFGPRN DKIKHVQNQV
61 DEVIDVMQEN ITKVIERGER LDELQDKSES LSDNATAFSN RSKQLRRQMW WRGCKIKAIM
121 ALVAAILLLV IIILIVMKYR TLocalizationUniProt · AlphaFold · HPA
Whether an antibody against VAMP4 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
- 1
- Mean surface accessibility (rSASA)
- 0.55
- Highest tissue expression
- 17 nTPM
Expression across tissuesHPA
Tissue
- cerebellum: 17 nTPM
- blood vessel: 17 nTPM
- pituitary gland: 14 nTPM
- cerebral cortex: 13 nTPM
- parathyroid gland: 12 nTPM
- adrenal gland: 11 nTPM
Single-cell type
- esophageal apical cells: 92 nCPM
- late spermatids: 60 nCPM
- late primary spermatocytes: 59 nCPM
- lactotrophs: 56 nCPM
- megakaryocytes: 50 nCPM
- platelets: 45 nCPM
Immune cell
- MAIT T-cell: 12 nTPM
- eosinophil: 12 nTPM
- memory CD4 T-cell: 11 nTPM
- T-reg: 11 nTPM
- basophil: 11 nTPM
- memory CD8 T-cell: 9.9 nTPM
Brain region
- thalamus: 26 nTPM
- cerebellum: 24 nTPM
- midbrain: 24 nTPM
- hypothalamus: 24 nTPM
- pons: 24 nTPM
- spinal cord: 24 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)
- 0.77
- gnomAD pLI
- 0.14
- gnomAD missense Z
- 0.68
- DepMap mean gene effect
- -0.08
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 11% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- cellular response to type II interferon
- endocytic recycling
- Golgi ribbon formation
- Golgi to plasma membrane protein transport
- neurotransmitter receptor transport, endosome to postsynaptic membrane
- regulation of synaptic vesicle endocytosis
- SNARE complex assembly
- synaptic vesicle to endosome fusion
- vesicle-mediated transport in synapse
- regulation of Golgi to plasma membrane protein transport
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Synaptobrevin-like
- v-SNARE, coiled-coil homology domain
- Synaptobrevin
- Vesicle-associated membrane protein 4
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of VAMP4 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 VAMP4 as an antibody target. Whether an autoantibody or antibody against VAMP4 could matter depends on whether native VAMP4 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
VAMP4 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 VAMP4 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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