GSK3B, glycogen synthase kinase 3 beta, 2932

N. diseases: 393; N. variants: 25
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs334558
rs334558
Entrez Id: 2932;107986119
Gene Symbol: GSK3B;LOC107986119
GSK3B;LOC107986119
CUI: C0525045
Disease:
Mood Disorders
0.010 GeneticVariation BEFREE A GSK3-beta promoter single-nucleotide polymorphism (rs334558) influences transcriptional strength, and the less active form was associated with less detrimental clinical features of mood disorders. 20113358 2010
dbSNP: rs334558
rs334558
Entrez Id: 2932;107986119
Gene Symbol: GSK3B;LOC107986119
GSK3B;LOC107986119
CUI: C1269683
Disease:
Major Depressive Disorder
0.020 GeneticVariation BEFREE Analysis of the genotyping data extracted from our hospital database revealed that rs334558 exhibited exclusive association with MDD in female patients (P=0.015).Our findings suggest that GSK3β rs334558 polymorphisms might be a potential risk for MDD, and females with GSK3β rs334558 polymorphisms might have higher penetrance of MDD. 28099358 2017
dbSNP: rs334558
rs334558
Entrez Id: 2932;107986119
Gene Symbol: GSK3B;LOC107986119
GSK3B;LOC107986119
CUI: C0686347
Disease:
Tardive Dyskinesia
0.010 GeneticVariation BEFREE Antipsychotic-induced TD was not associated with either of the tested functional polymorphisms (rs334558, rs1130214, and rs3730358). 30623492 2019
dbSNP: rs334558
rs334558
Entrez Id: 2932;107986119
Gene Symbol: GSK3B;LOC107986119
GSK3B;LOC107986119
CUI: C3714760
Disease:
Drug-induced tardive dyskinesia
0.010 GeneticVariation BEFREE Antipsychotic-induced TD was not associated with either of the tested functional polymorphisms (rs334558, rs1130214, and rs3730358). 30623492 2019
dbSNP: rs6805251
rs6805251
Entrez Id: 2932
Gene Symbol: GSK3B
GSK3B
CUI: C0392885
Disease:
High density lipoprotein measurement
T 0.800 GeneticVariation GWASCAT Association analyses of East Asian individuals and trans-ancestry analyses with European individuals reveal new loci associated with cholesterol and triglyceride levels. 28334899 2017
dbSNP: rs6438552
rs6438552
Entrez Id: 2932
Gene Symbol: GSK3B
GSK3B
CUI: C0040128
Disease:
Thyroid Diseases
0.010 GeneticVariation BEFREE Besides, logistic regression analysis demonstrated that rs12716927, rs5498 and rs6438552 all would affect the influences exerted by age, BMI, smoking history, stressful work, stress at home, family history of thyroid disease or <sup>131</sup>I treatment on GO susceptibility (all P < 0.05). 29800560 2018
dbSNP: rs6805251
rs6805251
Entrez Id: 2932
Gene Symbol: GSK3B
GSK3B
CUI: C0392885
Disease:
High density lipoprotein measurement
T 0.800 GeneticVariation GWASCAT Discovery and refinement of loci associated with lipid levels. 24097068 2013
dbSNP: rs6805251
rs6805251
Entrez Id: 2932
Gene Symbol: GSK3B
GSK3B
CUI: C0392885
Disease:
High density lipoprotein measurement
T 0.800 GeneticVariation GWASDB Discovery and refinement of loci associated with lipid levels. 24097068 2013
dbSNP: rs6805251
rs6805251
Entrez Id: 2932
Gene Symbol: GSK3B
GSK3B
CUI: C0428472
Disease:
Serum HDL cholesterol measurement
T 0.700 GeneticVariation GWASDB Discovery and refinement of loci associated with lipid levels. 24097068 2013
dbSNP: rs2199503
rs2199503
Entrez Id: 2932
Gene Symbol: GSK3B
GSK3B
CUI: C0524620
Disease:
Metabolic Syndrome X
0.010 GeneticVariation BEFREE Finally, we investigated the influence of interactions between ARNTL rs10832020, GSK3B rs2199503, PER3 rs10746473, and RORB rs972902 with environmental factors such as alcohol consumption, smoking status, and physical activity on MetS and its individual components (P < 0.001 ~ P = 0.002). 28296937 2017
dbSNP: rs6438552
rs6438552
Entrez Id: 2932
Gene Symbol: GSK3B
GSK3B
CUI: C0009402
Disease:
Colorectal Carcinoma
0.010 GeneticVariation BEFREE For the rs6438552 (T>C) polymorphism, the OR analysis showed that patients carrying C/T and C/C genotypes have a decreased risk for CRC (OR = 0.44, 95% CI: 0.27-0.70, P = 0.001 and OR = 0.24, 95% CI: 0.10-0.64, P = 0.001, respectively); this decreased risk was also evident in the stratified analysis by TNM stage and tumor location. 31679348 2019
dbSNP: rs6438552
rs6438552
Entrez Id: 2932
Gene Symbol: GSK3B
GSK3B
CUI: C0027651
Disease:
Neoplasms
0.010 GeneticVariation BEFREE For the rs6438552 (T>C) polymorphism, the OR analysis showed that patients carrying C/T and C/C genotypes have a decreased risk for CRC (OR = 0.44, 95% CI: 0.27-0.70, P = 0.001 and OR = 0.24, 95% CI: 0.10-0.64, P = 0.001, respectively); this decreased risk was also evident in the stratified analysis by TNM stage and tumor location. 31679348 2019
dbSNP: rs6782799
rs6782799
Entrez Id: 2932
Gene Symbol: GSK3B
GSK3B
CUI: C1269683
Disease:
Major Depressive Disorder
0.020 GeneticVariation BEFREE Further gene-gene interaction analyses showed a significant effect of a two-locus BDNF/GSK3B interaction with MDD (GSK3B rs6782799 and BDNF rs7124442) (corrected P = 0.011), and also for a three-locus interaction (GSK3B rs6782799, BDNF rs6265 and BDNF rs7124442) (corrected P = 0.019). 20033742 2010
dbSNP: rs140442947
rs140442947
Entrez Id: 2932
Gene Symbol: GSK3B
GSK3B
CUI: C0002395
Disease:
Alzheimer's Disease
C 0.700 GeneticVariation GWASCAT Genome-wide association study of Alzheimer's disease endophenotypes at prediagnosis stages. 29274321 2018
dbSNP: rs334558
rs334558
Entrez Id: 2932;107986119
Gene Symbol: GSK3B;LOC107986119
GSK3B;LOC107986119
CUI: C0917801
Disease:
Sleeplessness
0.010 GeneticVariation BEFREE GSK3B rs334558 was associated with insomnia but not with MDE severity in depressed patients. 30081294 2018
dbSNP: rs334558
rs334558
Entrez Id: 2932;107986119
Gene Symbol: GSK3B;LOC107986119
GSK3B;LOC107986119
CUI: C0024517
Disease:
Major depression, single episode
0.020 GeneticVariation BEFREE GSK3B rs334558 was associated with insomnia but not with MDE severity in depressed patients. 30081294 2018
dbSNP: rs6438552
rs6438552
Entrez Id: 2932
Gene Symbol: GSK3B
GSK3B
CUI: C0002395
Disease:
Alzheimer's Disease
0.020 GeneticVariation BEFREE GSK3β rs6438552 C>T polymorphism was correlated with increased the risk of developing AD only in Australian populations. 25351705 2015
dbSNP: rs334558
rs334558
Entrez Id: 2932;107986119
Gene Symbol: GSK3B;LOC107986119
GSK3B;LOC107986119
CUI: C0036341
Disease:
Schizophrenia
0.020 GeneticVariation BEFREE Here, by using meta-analysis we reported that glycogen synthase kinase 3β promoter inactive mutant rs334558 may contribute to the development of schizophrenia not bipolar disorder. 23440732 2013
dbSNP: rs6438552
rs6438552
Entrez Id: 2932
Gene Symbol: GSK3B
GSK3B
CUI: C0030567
Disease:
Parkinson Disease
0.050 GeneticVariation BEFREE However, among these interactions, individuals carrying the (C/C) genotype at both loci (rs6438552 and rs735555) had almost twice the risk of developing PD than those without this genotypic combination (OR, 1.871; 95% CI, 1.181-2.964; p = 0.009). 21130530 2012
dbSNP: rs334558
rs334558
Entrez Id: 2932;107986119
Gene Symbol: GSK3B;LOC107986119
GSK3B;LOC107986119
CUI: C0002395
Disease:
Alzheimer's Disease
0.050 GeneticVariation BEFREE However, little is known about the potential role of the GSK-3β rs334558 polymorphism, which has been associated with amnestic mild cognitive impairment (aMCI), which is itself associated with a high risk of AD. 22785398 2012
dbSNP: rs334558
rs334558
Entrez Id: 2932;107986119
Gene Symbol: GSK3B;LOC107986119
GSK3B;LOC107986119
CUI: C0030567
Disease:
Parkinson Disease
0.050 GeneticVariation BEFREE However, the analysis of rs334558 revealed that the risk of PD decreased in heterozygote, dominant or additive models (OR=0.60, 95% CI: 0.48, 0.74; OR=0.63, 95% CI: 0.51, 0.78; OR=0.82, 95% CI: 0.71, 0.94, respectively) from the Eastern Asian population. 23628795 2013
dbSNP: rs6438552
rs6438552
Entrez Id: 2932
Gene Symbol: GSK3B
GSK3B
CUI: C0030567
Disease:
Parkinson Disease
0.050 GeneticVariation BEFREE In a comparison of PD and control brains, there was increased in frequency of T allele (rs6438552) and corresponding increase in GSKDeltaexon9+11 and Tau phosphorylation in PD brains. 16315267 2005
dbSNP: rs12630592
rs12630592
Entrez Id: 2932
Gene Symbol: GSK3B
GSK3B
CUI: C0338831
Disease:
Manic
0.010 GeneticVariation BEFREE In mood disorder patients, the level of mania (in both acute and stabilized periods) and depression in stabilized periods was positively associated with GSK3B rs12630592 T only in FXR1 rs496250 A-allele carriers (Bonferroni-corrected interaction p=0.024, 0.052 and 0.017 respectively). 28242499 2017
dbSNP: rs12630592
rs12630592
Entrez Id: 2932
Gene Symbol: GSK3B
GSK3B
CUI: C0344315
Disease:
Depressed mood
0.010 GeneticVariation BEFREE In mood disorder patients, the level of mania (in both acute and stabilized periods) and depression in stabilized periods was positively associated with GSK3B rs12630592 T only in FXR1 rs496250 A-allele carriers (Bonferroni-corrected interaction p=0.024, 0.052 and 0.017 respectively). 28242499 2017
dbSNP: rs12630592
rs12630592
Entrez Id: 2932
Gene Symbol: GSK3B
GSK3B
CUI: C0011570
Disease:
Mental Depression
0.010 GeneticVariation BEFREE In mood disorder patients, the level of mania (in both acute and stabilized periods) and depression in stabilized periods was positively associated with GSK3B rs12630592 T only in FXR1 rs496250 A-allele carriers (Bonferroni-corrected interaction p=0.024, 0.052 and 0.017 respectively). 28242499 2017