SNAP25
Synaptosomal-associated protein 25
Also known as: bA416N4.2, dJ1068F16.2, RIC-4, RIC4, SEC9, SNAP, SNAP-25, SNP25_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- P60880
- Gene
- SNAP25
- Ensembl
- ENSG00000132639
- Chromosome
- 20
- Canonical length
- 206 aa
- Protein class
- Disease related genes, FDA approved drug targets, Human disease related genes, Predicted intracellular proteins, Transporters
- Subcellular location
- Vesicles,Plasma membrane
OverviewNCBI Gene
Synaptic vesicle membrane docking and fusion is mediated by SNAREs (soluble N-ethylmaleimide-sensitive factor attachment protein receptors) located on the vesicle membrane (v-SNAREs) and the target membrane (t-SNAREs). The assembled v-SNARE/t-SNARE complex consists of a bundle of four helices, one of which is supplied by v-SNARE and the other three by t-SNARE. For t-SNAREs on the plasma membrane, the protein syntaxin supplies one helix and the protein encoded by this gene contributes the other two. Therefore, this gene product is a presynaptic plasma membrane protein involved in the regulation of neurotransmitter release. Two alternative transcript variants encoding different protein isoforms have been described for this gene. [provided by RefSeq, Jul 2008]
Canonical amino-acid sequenceUniProt
206 residues, UniProt reviewed canonical sequence.
>P60880|SNAP25
1 MAEDADMRNE LEEMQRRADQ LADESLESTR RMLQLVEESK DAGIRTLVML DEQGEQLERI
61 EEGMDQINKD MKEAEKNLTD LGKFCGLCVC PCNKLKSSDA YKKAWGNNQD GVVASQPARV
121 VDEREQMAIS GGFIRRVTND ARENEMDENL EQVSGIIGNL RHMALDMGNE IDTQNRQIDR
181 IMEKADSNKT RIDEANQRAT KMLGSGLocalizationUniProt · AlphaFold · HPA
Whether an antibody against SNAP25 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)
- 0.42
- Highest tissue expression
- 2,270 nTPM
Expression across tissuesHPA
Tissue
- cerebellum: 2,270 nTPM
- cerebral cortex: 1,847 nTPM
- hippocampal formation: 896 nTPM
- amygdala: 845 nTPM
- basal ganglia: 570 nTPM
- retina: 443 nTPM
Single-cell type
- brain excitatory neurons: 1,192 nCPM
- retinal bipolar cells: 837 nCPM
- lactotrophs: 743 nCPM
- brain inhibitory neurons: 676 nCPM
- gonadotrophs: 584 nCPM
- somatotrophs: 580 nCPM
Immune cell
- basophil: 0.6 nTPM
- plasmacytoid DC: 0.2 nTPM
- eosinophil: 0.1 nTPM
- classical monocyte: 0 nTPM
- gdT-cell: 0 nTPM
- intermediate monocyte: 0 nTPM
Brain region
- cerebral cortex: 3,924 nTPM
- white matter: 1,928 nTPM
- cerebellum: 1,629 nTPM
- pons: 1,334 nTPM
- hippocampal formation: 1,153 nTPM
- basal ganglia: 901 nTPM
DiseaseUniProt · ClinVar · IEDB · PubMed
Four sources answering four different questions about SNAP25.
Disease | AllUniProt
Conditions SNAP25 is implicated in, by any mechanism.
- Developmental and epileptic encephalopathy 117 (DEE117) MIM:616330
Disease | GeneticClinVar
26 pathogenic / likely-pathogenic of 257 ClinVar records.
Conditions with pathogenic or likely-pathogenic variants.
- Developmental and epileptic encephalopathy
- Congenital myasthenic syndrome 18
- Inborn genetic diseases
- Focal epilepsy
- Unilateral Hypotonia
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)
- 0.23
- gnomAD pLI
- 0.99
- gnomAD missense Z
- 2.96
- DepMap mean gene effect
- 0.01
- 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
- associative learning
- chemical synaptic transmission
- exocytosis
- locomotory behavior
- long-term synaptic potentiation
- neurotransmitter uptake
- presynaptic dense core vesicle exocytosis
- regulation of insulin secretion
- regulation of neuron projection development
- synaptic vesicle docking
- synaptic vesicle exocytosis
- synaptic vesicle fusion to presynaptic active zone membrane
- synaptic vesicle priming
Molecular functions
- calcium-dependent protein binding
- lipid binding
- SNAP receptor activity
- syntaxin-1 binding
- voltage-gated potassium channel activity
Cellular components
- cell cortex
- cytoplasm
- cytoskeleton
- cytosol
- glutamatergic synapse
- growth cone
- membrane
- neuron projection
- perinuclear region of cytoplasm
- photoreceptor inner segment
- plasma membrane
- presynaptic membrane
- ribbon synapse
- SNARE complex
- somatodendritic compartment
- specific granule membrane
- synaptic vesicle
- synaptobrevin 2-SNAP-25-syntaxin-1a-complexin I complex
- tertiary granule membrane
- trans-Golgi network
Protein domainsUniProt · Pfam · InterPro
- Target SNARE coiled-coil homology domain
- SNAP-25 domain
- SNAP-25 family
- SNAP25, N-terminal SNARE motif, chordates
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of SNAP25 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 SNAP25 as an antibody target. Whether an autoantibody or antibody against SNAP25 could matter depends on whether native SNAP25 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
SNAP25 is annotated at the cell surface, where native SNAP25 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 SNAP25 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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