SNAP47
Synaptosomal-associated protein 47
Also known as: C1orf142, SNAP-47, SNP47_HUMAN, SVAP1
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q5SQN1
- Gene
- SNAP47
- Ensembl
- ENSG00000143740
- Chromosome
- 1
- Canonical length
- 464 aa
- Protein class
- Predicted intracellular proteins, Predicted membrane proteins
- Subcellular location
- Cytosol
OverviewNCBI Gene
Predicted to enable SNAP receptor activity and syntaxin binding activity. Predicted to be involved in synaptic vesicle fusion to presynaptic active zone membrane and synaptic vesicle priming. Predicted to act upstream of or within long-term synaptic potentiation. Located in BLOC-1 complex. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
464 residues, UniProt reviewed canonical sequence.
>Q5SQN1|SNAP47
1 MRAARRGLHC AGAERPRRRG RLWDSSGVPQ RQKRPGPWRT QTQEQMSRDV CIHTWPCTYY
61 LEPKRRWVTG QLSLTSLSLR FMTDSTGEIL VSFPLSSIVE IKKEASHFIF SSITILEKGH
121 AKHWFSSLRP SRNVVFSIIE HFWRELLLSQ PGAVADASVP RTRGEELTGL MAGSQKRLED
181 TARVLHHQGQ QLDSVMRGLD KMESDLEVAD RLLTELESPA WWPFSSKLWK TPPETKPRED
241 VSMTSCEPFG KEGILIKIPA VISHRTESHV KPGRLTVLVS GLEIHDSSSL LMHRFEREDV
301 DDIKVHSPYE ISIRQRFIGK PDMAYRLISA KMPEVIPILE VQFSKKMELL EDALVLRSAR
361 TSSPAEKSCS VWHAASGLMG RTLHREPPAG DQEGTALHLQ TSLPALSEAD TQELTQILRR
421 MKGLALEAES ELERQDEALD GVAAAVDRAT LTIDKHNRRM KRLTLocalizationUniProt · AlphaFold · HPA
Whether an antibody against SNAP47 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
- Intracellular
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.44
- Highest tissue expression
- 45 nTPM
Expression across tissuesHPA
Tissue
- ovary: 45 nTPM
- cerebral cortex: 41 nTPM
- adrenal gland: 39 nTPM
- basal ganglia: 38 nTPM
- heart muscle: 36 nTPM
- skeletal muscle: 36 nTPM
Single-cell type
- late spermatids: 142 nCPM
- late primary spermatocytes: 82 nCPM
- cardiomyocytes: 70 nCPM
- early spermatids: 64 nCPM
- breast lactating cells: 63 nCPM
- ovarian stromal cells: 61 nCPM
Immune cell
- T-reg: 47 nTPM
- memory CD8 T-cell: 34 nTPM
- eosinophil: 34 nTPM
- memory CD4 T-cell: 33 nTPM
- NK-cell: 31 nTPM
- gdT-cell: 30 nTPM
Brain region
- cerebral cortex: 40 nTPM
- hippocampal formation: 38 nTPM
- basal ganglia: 38 nTPM
- amygdala: 30 nTPM
- cerebellum: 30 nTPM
- white matter: 28 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)
- 0.99
- gnomAD pLI
- 0
- gnomAD missense Z
- -0.13
- DepMap mean gene effect
- -0.04
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 17% 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
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of SNAP47 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 SNAP47 as an antibody target. Whether an autoantibody or antibody against SNAP47 could matter depends on whether native SNAP47 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
SNAP47 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 SNAP47 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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