STX3 (syntaxin 3)

2016-10-01  

Identity

HGNC
LOCATION
11q12.1
LOCUSID
ALIAS
STX3A
FUSION GENES

Other Information

Locus ID:

NCBI: 6809
MIM: 600876
HGNC: 11438
Ensembl: ENSG00000166900

Variants:

dbSNP: 6809
ClinVar: 6809
TCGA: ENSG00000166900
COSMIC: STX3

RNA/Proteins

Gene IDTranscript IDUniprot
ENSG00000166900ENST00000337979Q13277
ENSG00000166900ENST00000337979Q53YE2
ENSG00000166900ENST00000528805A0A0C4DGE4
ENSG00000166900ENST00000529177Q13277
ENSG00000166900ENST00000530221E9PN33
ENSG00000166900ENST00000533637E9PQJ8
ENSG00000166900ENST00000633708A0A0J9YW33
ENSG00000166900ENST00000641815A0A286YF28

Expression (GTEx)

0
5
10
15
20
25
30
35
40
45

Pathways

PathwaySourceExternal ID
SNARE interactions in vesicular transportKEGGko04130
SNARE interactions in vesicular transportKEGGhsa04130
Synaptic vesicle cycleKEGGko04721
Synaptic vesicle cycleKEGGhsa04721
Immune SystemREACTOMER-HSA-168256
Cytokine Signaling in Immune systemREACTOMER-HSA-1280215
Signaling by InterleukinsREACTOMER-HSA-449147

Protein levels (Protein atlas)

Not detected
Low
Medium
High

References

Pubmed IDYearTitleCitations
380144872023Increased STX3 transcript and protein levels were associated with poor prognosis in two independent cohorts of esophageal squamous cell carcinoma patients.1
380144872023Increased STX3 transcript and protein levels were associated with poor prognosis in two independent cohorts of esophageal squamous cell carcinoma patients.1
339741302021Pathogenic STX3 variants affecting the retinal and intestinal transcripts cause an early-onset severe retinal dystrophy in microvillus inclusion disease subjects.12
339741302021Pathogenic STX3 variants affecting the retinal and intestinal transcripts cause an early-onset severe retinal dystrophy in microvillus inclusion disease subjects.12
312019482019Interaction networks of Weibel-Palade body regulators syntaxin-3 and syntaxin binding protein 5 in endothelial cells.3
312019482019Interaction networks of Weibel-Palade body regulators syntaxin-3 and syntaxin binding protein 5 in endothelial cells.3
294085952018STX3 represses the stability of the tumor suppressor PTEN to activate the PI3K-Akt-mTOR signaling and promotes the growth of breast cancer cells.14
294759512018Soluble syntaxin 3 functions as a transcriptional regulator.9
298804882018Weibel-Palade Body Localized Syntaxin-3 Modulates Von Willebrand Factor Secretion From Endothelial Cells.22
294085952018STX3 represses the stability of the tumor suppressor PTEN to activate the PI3K-Akt-mTOR signaling and promotes the growth of breast cancer cells.14
294759512018Soluble syntaxin 3 functions as a transcriptional regulator.9
298804882018Weibel-Palade Body Localized Syntaxin-3 Modulates Von Willebrand Factor Secretion From Endothelial Cells.22
253584292015Autosomal recessive congenital cataract, intellectual disability phenotype linked to STX3 in a consanguineous Tunisian family.11
255482522015An essential role of syntaxin 3 protein for granule exocytosis and secretion of IL-1α, IL-1β, IL-12b, and CCL4 from differentiated HL-60 cells.19
255833872015Human cytomegalovirus miR-US33-5p inhibits viral DNA synthesis and viral replication by down-regulating expression of the host Syntaxin3.12

Citation

Dessen P

STX3 (syntaxin 3)

Atlas Genet Cytogenet Oncol Haematol. 2016-10-01

Online version: http://atlasgeneticsoncology.org/gene/56217/deep-insight-explorer/js/_common.js