STX6, syntaxin 6, 10228

N. diseases: 19; N. variants: 3
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0038868
Disease: Progressive supranuclear palsy
Progressive supranuclear palsy
0.430 GeneticVariation disease GWASCAT Joint genome-wide association study of progressive supranuclear palsy identifies novel susceptibility loci and genetic correlation to neurodegenerative diseases. 30089514 2018
CUI: C0038868
Disease: Progressive supranuclear palsy
Progressive supranuclear palsy
0.430 Biomarker disease BEFREE The objective of this study was to investigate the effect of genes previously identified as risk alleles, including microtubule-associated protein tau, myelin-associated oligodendrocyte basic protein, eukaryotic translation initiation factor 2-alpha kinase 3, and syntaxin 6, as well as apolipoprotein E, on cognitive function in progressive supranuclear palsy. 29076559 2017
CUI: C0038868
Disease: Progressive supranuclear palsy
Progressive supranuclear palsy
0.430 GeneticVariation disease BEFREE A variant in Syntaxin 6 (a soluble N-ethylmaleimide-sensitive factor attachment protein receptor STX6) (rs1411478) has been shown to be associated with progressive supranuclear palsy (PSP). 23415606 2013
CUI: C0038868
Disease: Progressive supranuclear palsy
Progressive supranuclear palsy
0.430 Biomarker disease CTD_human We found significant previously unidentified signals (P < 5 × 10(-8)) associated with PSP risk at STX6, EIF2AK3 and MOBP. 21685912 2011
CUI: C0038868
Disease: Progressive supranuclear palsy
Progressive supranuclear palsy
0.430 GeneticVariation disease GWASDB We found significant previously unidentified signals (P < 5 × 10(-8)) associated with PSP risk at STX6, EIF2AK3 and MOBP. 21685912 2011
CUI: C0038868
Disease: Progressive supranuclear palsy
Progressive supranuclear palsy
0.430 GeneticVariation disease BEFREE We found significant previously unidentified signals (P < 5 × 10(-8)) associated with PSP risk at STX6, EIF2AK3 and MOBP. 21685912 2011
CUI: C0038868
Disease: Progressive supranuclear palsy
Progressive supranuclear palsy
0.430 GeneticVariation disease GWASCAT We found significant previously unidentified signals (P < 5 × 10(-8)) associated with PSP risk at STX6, EIF2AK3 and MOBP. 21685912 2011
CUI: C1866282
Disease: CEROID LIPOFUSCINOSIS, NEURONAL, 6
CEROID LIPOFUSCINOSIS, NEURONAL, 6
0.300 Biomarker disease CTD_human Increased zinc and manganese in parallel with neurodegeneration, synaptic protein changes and activation of Akt/GSK3 signaling in ovine CLN6 neuronal ceroid lipofuscinosis. 23516525 2013
Ophthalmoplegia, Progressive Supranuclear
0.300 Biomarker disease CTD_human Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy. 21685912 2011
CUI: C4551863
Disease: Supranuclear Palsy, Progressive, 1
Supranuclear Palsy, Progressive, 1
0.300 Biomarker disease CTD_human Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy. 21685912 2011
CUI: C1629609
Disease: Age at menopause
Age at menopause
0.100 GeneticVariation phenotype GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
CUI: C1629609
Disease: Age at menopause
Age at menopause
0.100 GeneticVariation phenotype GWASCAT Large-scale genomic analyses link reproductive aging to hypothalamic signaling, breast cancer susceptibility and BRCA1-mediated DNA repair. 26414677 2015
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.020 Biomarker group BEFREE The Cancer Genome Atlas analysis showed increased syntaxin 6 expressions associated with higher Gleason score and decreased progression-free survival in PCa patients. 31674708 2020
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
0.020 Biomarker group BEFREE The Cancer Genome Atlas analysis showed increased syntaxin 6 expressions associated with higher Gleason score and decreased progression-free survival in PCa patients. 31674708 2020
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.020 AlteredExpression group BEFREE STX6 is overexpressed in many types of human cancer. 22573826 2012
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
0.020 AlteredExpression group BEFREE STX6 is overexpressed in many types of human cancer. 22573826 2012
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
0.010 Biomarker disease BEFREE Syntaxin 6-mediated exosome secretion regulates enzalutamide resistance in prostate cancer. 31674708 2020
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma
0.010 Biomarker disease BEFREE Syntaxin 6-mediated exosome secretion regulates enzalutamide resistance in prostate cancer. 31674708 2020
CUI: C0007134
Disease: Renal Cell Carcinoma
Renal Cell Carcinoma
0.010 AlteredExpression disease BEFREE When stratifying the data based on histological subtype, the papillary RCC subtype exhibited a significant correlation between syntaxin 6 expression and survival. 30816681 2019
Conventional (Clear Cell) Renal Cell Carcinoma
0.010 AlteredExpression disease BEFREE When stratifying the data based on histological subtype, the papillary RCC subtype exhibited a significant correlation between syntaxin 6 expression and survival. 30816681 2019
CUI: C0003811
Disease: Cardiac Arrhythmia
Cardiac Arrhythmia
0.010 Biomarker phenotype BEFREE Thus, our studies reveals that trafficking-related gene Stx6 may regulate intracellular calcium and is involved in the occurrence of cardiac arrhythmia, which provides new insights in that miR-1 participates in arrhythmia by regulating the trafficking-related genes and pathway. 28397788 2017
CUI: C0004623
Disease: Bacterial Infections
Bacterial Infections
0.010 Biomarker group BEFREE These findings demonstrate that RABGEF1 mediates RE fusion with GcAVs through the STX6-VAMP3-VTI1B complex, and reveal the SNARE dynamics involved in autophagosome formation in response to bacterial infection. 27791468 2017
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.010 Biomarker disease BEFREE Moreover, we found that Stx6 was decreased in the heart of mice after myocardial infarction and in the hypoxic cardiomyocytes, and further confirmed that Stx6 is a target of miR-1. 28397788 2017
Adverse Event Associated with Cardiac Arrhythmia
0.010 Biomarker phenotype BEFREE Thus, our studies reveals that trafficking-related gene Stx6 may regulate intracellular calcium and is involved in the occurrence of cardiac arrhythmia, which provides new insights in that miR-1 participates in arrhythmia by regulating the trafficking-related genes and pathway. 28397788 2017
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.010 AlteredExpression group BEFREE Here, we have found that the expression of STX6 was up-regulated in ESCC samples, its expression was significantly correlated with tumor size, histological differentiation, lymph node metastasis and depth. 26906622 2016