Annotation inferences using phylogenetic trees

Gene Ontology annotation based on curation of immunofluorescence data

Automatic transfer of experimentally verified manual GO annotation data to orthologs using Ensembl Compara

Automatic assignment of GO terms using logical inference, based on on inter-ontology links

Electronic Gene Ontology annotations created by ARBA machine learning models

Combined Automated Annotation using Multiple IEA Methods

A role for Sec1/Munc18 proteins in platelet exocytosis.

Towards a proteome-scale map of the human protein-protein interaction network.

A critical role for vesicle-associated membrane protein-7 in exocytosis from human eosinophils and neutrophils.

Vesicle associated membrane protein (VAMP)-7 and VAMP-8, but not VAMP-2 or VAMP-3, are required for activation-induced degranulation of mature human mast cells.

Heterogeneous expression of SNARE proteins SNAP-23, SNAP-25, Syntaxin1 and VAMP in human parathyroid tissue.

Involvement of Munc18 isoforms in the regulation of granule exocytosis in neutrophils.

Large-scale proteomics and phosphoproteomics of urinary exosomes.

MHC class II-associated proteins in B-cell exosomes and potential functional implications for exosome biogenesis.

Analysis of the myosin-II-responsive focal adhesion proteome reveals a role for β-Pix in negative regulation of focal adhesion maturation.

A directed protein interaction network for investigating intracellular signal transduction.

SNAP-23 and VAMP-3 contribute to the release of IL-6 and TNFα from a human synovial sarcoma cell line.

The palmitoyl acyltransferase HIP14 shares a high proportion of interactors with huntingtin: implications for a role in the pathogenesis of Huntington's disease.

A proteome-scale map of the human interactome network.

E-cadherin interactome complexity and robustness resolved by quantitative proteomics.

The Q-soluble N-Ethylmaleimide-sensitive Factor Attachment Protein Receptor (Q-SNARE) SNAP-47 Regulates Trafficking of Selected Vesicle-associated Membrane Proteins (VAMPs).

Immunofluorescence microscopy of SNAP23 in human skeletal muscle reveals colocalization with plasma membrane, lipid droplets, and mitochondria.

Munc18-2 is required for Syntaxin 11 Localization on the Plasma Membrane in Cytotoxic T-Lymphocytes.

SM protein Munc18-2 facilitates transition of Syntaxin 11-mediated lipid mixing to complete fusion for T-lymphocyte cytotoxicity.

Syntaxin 11 regulates the stimulus-dependent transport of Toll-like receptor 4 to the plasma membrane by cooperating with SNAP-23 in macrophages.

A protein-interaction network of interferon-stimulated genes extends the innate immune system landscape.

A reference map of the human binary protein interactome.

Dual proteome-scale networks reveal cell-specific remodeling of the human interactome.

OpenCell: Endogenous tagging for the cartography of human cellular organization.

Multimodal cell maps as a foundation for structural and functional genomics.

Vamp7 associated Lysosome to Plasma membrane transport

Vamp8 associated secretory vesicle to plasma membrane transport

Vamp2 associated secretory vesicle to plasma membrane transport

Exocytosis of tertiary granule membrane proteins

Exocytosis of specific granule membrane proteins

IKKB phosphorylates SNAP23

Fusion of ERC and phagosome

Identification of a novel syntaxin- and synaptobrevin/VAMP-binding protein, SNAP-23, expressed in non-neuronal tissues.

Identification of two isoforms of the vesicle-membrane fusion protein SNAP-23 in human neutrophils and HL-60 cells.

Syntaxin 11 is associated with SNAP-23 on late endosomes and the trans-Golgi network.

Genomic organization, chromosomal localization, alternative splicing, and isoforms of the human synaptosome-associated protein-23 gene implicated in vesicle-membrane fusion processes.

Homotetrameric structure of the SNAP-23 N-terminal coiled-coil domain.

Site-specific analysis of protein S-acylation by resin-assisted capture.

Analysis of familial hemophagocytic lymphohistiocytosis type 4 (FHL-4) mutant proteins reveals that S-acylation is required for the function of syntaxin 11 in natural killer cells.

UniProtKB entry O00161 (SNAP23_HUMAN)