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GeneE
10 sources retrieved · Most recent: April 2026 · Index updated 14 days ago
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STX17
syntaxin 17
Chromosome 9 · 9q31.1
NCBI Gene: 55014Ensembl: ENSG00000136874.12HGNC: HGNC:11432UniProt: P56962
85PubMed Papers
20Diseases
0Drugs
0Pathogenic Variants
FUNCTIONAL ROLE
Hub GeneTransporter
DATA QUALITY
✓ Experimental GO Evidence✓ Swiss-Prot Reviewed
mitochondrionlysosomal membranerough endoplasmic reticulumprotein localization to phagophore assembly siteplacenta praeviaage-related macular degenerationinsomniaovarian neoplasm
✦AI Summary

STX17 (syntaxin 17) is a SNARE protein essential for autophagosome-lysosome fusion in autophagy. As a soluble N-ethylmaleimide-sensitive factor-attachment protein receptor, STX17 localizes on the autophagosome membrane and assembles with partner SNAREs to form trans-SNARE complexes that drive membrane fusion 123. STX17 directly controls autophagosome maturation by mediating fusion with lysosomal membranes, a critical step for degrading cellular cargo 12. Recent mechanistic studies reveal that STX17 forms a priming complex with SNAP29 and YKT6 on autophagosomes, which is subsequently displaced by VAMP8 to create the fusogenic STX17-SNAP29-VAMP8 complex 4. STX17 recruitment to ER-mitochondria contact sites, mediated by binding to ATG14, is crucial for autophagosome biogenesis 5. Beyond autophagy, STX17 maintains ER-Golgi intermediate compartment (ERGIC) architecture and regulates early secretory pathway transport 6. Dysregulation of STX17 has disease implications: zinc influx through MCOLN1 disrupts STX17-VAMP8 interaction, arresting autophagic flux in cancer cells 7, while altered STX17 expression affects macrophage autophagy maturation in allergic asthma 8. Post-translational acetylation of STX17 regulates autophagosome-lysosome fusion efficiency 9.

Sources cited
1
STX17 is a SNARE of the autophagosome involved in autophagy through autophagosome-lysosome fusion
PMID: 23217709
2
STX17 mediates autophagosome membrane fusion with lysosome membrane as part of SNARE complex formation
PMID: 25686604
3
SNAREs including STX17 form trans-SNARE complexes that drive autophagosome-lysosome membrane fusion
PMID: 28306502
4
YKT6 forms a priming complex with STX17 and SNAP29, which is displaced by VAMP8 to form the fusogenic STX17-SNAP29-VAMP8 complex
PMID: 38340317
5
STX17 binds ATG14 and recruits it to ER-mitochondria contact sites important for autophagosome formation
PMID: 23455425
6
STX17 may maintain architecture of ER-Golgi intermediate compartment and regulate transport between ER, ERGIC and Golgi
PMID: 21545355
7
Zinc influx through MCOLN1 blocks interaction between STX17 and VAMP8, disrupting autophagosome-lysosome fusion in cancer
PMID: 33890549
8
METTL3/YTHDF3-m6A/PTX3 interactions contribute to autophagy maturation in macrophages by modulating STX17 expression in allergic asthma
PMID: 37957139
9
Acetylation occurs on STX17, a key protein participating in autophagosome-lysosome fusion
PMID: 35435793
Disease Associationsⓘ20
placenta praeviaOpen Targets
0.30Weak
age-related macular degenerationOpen Targets
0.30Weak
insomniaOpen Targets
0.27Weak
ovarian neoplasmOpen Targets
0.25Weak
otosclerosisOpen Targets
0.24Weak
atrial fibrillationOpen Targets
0.15Weak
cervical carcinomaOpen Targets
0.11Weak
lung diseaseOpen Targets
0.06Suggestive
Failure to thriveOpen Targets
0.05Suggestive
squamous cell carcinomaOpen Targets
0.05Suggestive
frozen shoulderOpen Targets
0.05Suggestive
Alzheimer diseaseOpen Targets
0.05Suggestive
diabetic ketoacidosisOpen Targets
0.04Suggestive
renal cell carcinomaOpen Targets
0.04Suggestive
liver diseaseOpen Targets
0.04Suggestive
ulcerative colitisOpen Targets
0.04Suggestive
inflammatory bowel diseaseOpen Targets
0.04Suggestive
peritonitisOpen Targets
0.04Suggestive
infectionOpen Targets
0.04Suggestive
atopic eczemaOpen Targets
0.03Suggestive
Pathogenic Variants
No pathogenic variants reported on ClinVar for this gene.
View on ClinVar ↗
Related Genes
VAMP4Protein interaction100%SCFD1Protein interaction100%ULK1Protein interaction100%VPS11Protein interaction100%VPS16Protein interaction100%VTI1AProtein interaction100%
Tissue Expression6 tissues
Heart
100%
Liver
89%
Brain
82%
Ovary
82%
Bone Marrow
69%
Lung
67%
Gene Interaction Network
Click a node to explore
STX17VAMP4SCFD1ULK1VPS11VPS16VTI1A
PROTEIN STRUCTURE
Preparing viewer…
PDB4WY4 · 1.40 Å · X-ray
View on RCSB ↗
Constraintⓘ
LOEUFⓘ
1.08LoF Tolerant
pLIⓘ
0.00Tolerant
Observed/Expected LoF0.79 [0.58–1.08]
RankingsWhere STX17 stands among ~20K protein-coding genes
  • #5,640of 20,598
    Most Researched85
  • #10,993of 17,882
    Most Constrained (LOEUF)1.08
Genes detectedSTX17
Sources retrieved10 papers
Response time—
📄 Sources
10▼
1
Acetylation in the regulation of autophagy.
PMID: 35435793
Autophagy · 2023
1.00
2
Dysfunction of autophagy in high-fat diet-induced non-alcoholic fatty liver disease.
PMID: 37700498
Autophagy · 2024
0.90
3
Human YKT6 forms priming complex with STX17 and SNAP29 to facilitate autophagosome-lysosome fusion.
PMID: 38340317
Cell Rep · 2024
0.80
4
Autophagosomes form at ER-mitochondria contact sites.
PMID: 23455425
Nature · 2013
0.70
5
MCOLN1/TRPML1 finely controls oncogenic autophagy in cancer by mediating zinc influx.
PMID: 33890549
Autophagy · 2021
0.60