FKBP5, FKBP prolyl isomerase 5, 2289

N. diseases: 179; N. variants: 20
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1360780
rs1360780
Entrez Id: 2289;112267956
Gene Symbol: FKBP5;LOC112267956
FKBP5;LOC112267956
CUI: C1269683
Disease:
Major Depressive Disorder
0.090 GeneticVariation BEFREE Significant associations between AD and MDD have been found for three polymorphisms mainly in females (TPH1 A218C, MAOA VNTR and BDNF Val66Met) and one polymorphism in the total population only (FKBP5 rs1360780). 23157339 2013
dbSNP: rs1360780
rs1360780
Entrez Id: 2289;112267956
Gene Symbol: FKBP5;LOC112267956
FKBP5;LOC112267956
CUI: C1269683
Disease:
Major Depressive Disorder
0.090 GeneticVariation BEFREE The results showed that the T allele of rs1360780 was more frequent among the patients affected by MDD with a comorbidity of anxiety disorders, compared to those without (P < .001). 23861224 2013
dbSNP: rs1360780
rs1360780
Entrez Id: 2289;112267956
Gene Symbol: FKBP5;LOC112267956
FKBP5;LOC112267956
CUI: C0011581
Disease:
Depressive disorder
0.090 GeneticVariation BEFREE The significant interaction between ELA and the rs1360780 polymorphism in HATA suggests a role of FKBP5 in the pathophysiology of structural alterations in depression. 30986730 2019
dbSNP: rs1360780
rs1360780
Entrez Id: 2289;112267956
Gene Symbol: FKBP5;LOC112267956
FKBP5;LOC112267956
CUI: C1269683
Disease:
Major Depressive Disorder
0.090 GeneticVariation BEFREE The rs1360780 SNP in this gene (T allele vs C homozygous) has been found to be associated with major depressive disorder (MDD). 26076833 2016
dbSNP: rs1360780
rs1360780
Entrez Id: 2289;112267956
Gene Symbol: FKBP5;LOC112267956
FKBP5;LOC112267956
CUI: C0011581
Disease:
Depressive disorder
0.090 GeneticVariation BEFREE The FKBP5 rs1360780 polymorphism is associated with plasma cortisol and FKBP5 mRNA expression after psychosocial stress in healthy controls but not in remitted depression. 25522420 2014
dbSNP: rs1360780
rs1360780
Entrez Id: 2289;112267956
Gene Symbol: FKBP5;LOC112267956
FKBP5;LOC112267956
CUI: C0011581
Disease:
Depressive disorder
0.090 GeneticVariation BEFREE Childhood adversity showed an interaction with the brain-derived neurotrophic factor (BDNF) gene Val66Met polymorphism, serotonin transporter-linked promoter region (5-HTTLPR), and FK506 binding protein 51 (FKBP5) gene rs1360780 in brain morphologic changes in patients with depression and in a non-clinical population. 29535036 2019
dbSNP: rs1360780
rs1360780
Entrez Id: 2289;112267956
Gene Symbol: FKBP5;LOC112267956
FKBP5;LOC112267956
CUI: C1269683
Disease:
Major Depressive Disorder
0.090 GeneticVariation BEFREE We investigated the interactive effects of FKBP5 rs1360780 allelic variants, DNA methylation, and the diagnosis of MDD on structural changes of the entire brain. 28198448 2017
dbSNP: rs1360780
rs1360780
Entrez Id: 2289;112267956
Gene Symbol: FKBP5;LOC112267956
FKBP5;LOC112267956
CUI: C1269683
Disease:
Major Depressive Disorder
0.090 GeneticVariation BEFREE In the present study, we investigated whether the FKBP5 polymorphism rs1360780 and lifetime history of major depression are associated with DNA methylation and FKBP5 gene expression after psychosocial stress. 25522420 2014
dbSNP: rs1360780
rs1360780
Entrez Id: 2289;112267956
Gene Symbol: FKBP5;LOC112267956
FKBP5;LOC112267956
CUI: C0011581
Disease:
Depressive disorder
0.090 GeneticVariation BEFREE FKBP5:rs1360780 allele T and genotype TT were overrepresented in depression for men. 20226536 2010
dbSNP: rs1360780
rs1360780
Entrez Id: 2289;112267956
Gene Symbol: FKBP5;LOC112267956
FKBP5;LOC112267956
CUI: C0011581
Disease:
Depressive disorder
0.090 GeneticVariation BEFREE The aim of our study was to explore the role of the FKBP5 gene variants (rs1360780, rs3800373 and rs4713916), in depressive disorders or suicidal behavior through a systematic review and a meta-analysis. 30791339 2019
dbSNP: rs1360780
rs1360780
Entrez Id: 2289;112267956
Gene Symbol: FKBP5;LOC112267956
FKBP5;LOC112267956
CUI: C1269683
Disease:
Major Depressive Disorder
0.090 GeneticVariation BEFREE However, after removing one heterogeneous German study, as indicated by sensitivity analysis, both the rs1360780 T-allele (Z = 2.95, P = 0.003, OR = 1.06, 95% CI = 1.02-1.11) and the rs3800373 C-allele (Z = 3.05, P = 0.002, OR = 1.07, 95% CI 1.02-1.12) were significantly associated with MDD in a fixed-effect model. 27601205 2016
dbSNP: rs1360780
rs1360780
Entrez Id: 2289;112267956
Gene Symbol: FKBP5;LOC112267956
FKBP5;LOC112267956
CUI: C0011581
Disease:
Depressive disorder
0.090 GeneticVariation BEFREE Third, there is an additive interaction effect between FKBP5's rs1360780 variant and the graph-theoretical metrics of hippocampal connectivity to influence depression risk. 26801675 2017
dbSNP: rs1360780
rs1360780
Entrez Id: 2289;112267956
Gene Symbol: FKBP5;LOC112267956
FKBP5;LOC112267956
CUI: C0011581
Disease:
Depressive disorder
0.090 GeneticVariation BEFREE Given the large effect sizes, rs1360780 could be included into prediction models for depression in individuals exposed to childhood abuse. 21654733 2011
dbSNP: rs1360780
rs1360780
Entrez Id: 2289;112267956
Gene Symbol: FKBP5;LOC112267956
FKBP5;LOC112267956
CUI: C0011581
Disease:
Depressive disorder
0.090 GeneticVariation BEFREE To investigate the possible relationship between genetic risk factors and depression in AD, we assessed genetic polymorphisms reported to be associated with depression (MAOA VNTR, ACE 288bp Insertion/ Deletion, 5HTTLPR, COMT Val158Met, BDNF Val66Met, TPH1 A218C, HTR2A T102C, P2RX7 Q460R, FKBP5 rs1360780 and CRHR1 rs242941) in a cross-sectional study on 246 AD patients with or without clinically significant major depressive disorder (MDD) according to DSM-IV. 23157339 2013
dbSNP: rs1360780
rs1360780
Entrez Id: 2289;112267956
Gene Symbol: FKBP5;LOC112267956
FKBP5;LOC112267956
CUI: C1269683
Disease:
Major Depressive Disorder
0.090 GeneticVariation BEFREE The FKBP5 polymorphism rs1360780 influences the effect of an algorithm-based antidepressant treatment and is associated with remission in patients with major depression. 26645208 2016
dbSNP: rs1360780
rs1360780
Entrez Id: 2289;112267956
Gene Symbol: FKBP5;LOC112267956
FKBP5;LOC112267956
CUI: C1269683
Disease:
Major Depressive Disorder
0.090 GeneticVariation BEFREE Change in FKBP5 expression correlated with change in Beck Depression Inventory (BDI) for MDD → euthymic comparison in GG genotype of rs3800373 (P = .013) and TT carriers of rs1360780 (P = .02). 20726698 2010
dbSNP: rs1360780
rs1360780
Entrez Id: 2289;112267956
Gene Symbol: FKBP5;LOC112267956
FKBP5;LOC112267956
CUI: C1269683
Disease:
Major Depressive Disorder
0.090 GeneticVariation BEFREE We investigated the effects of the rs1360780 polymorphism of the hypothalamic-pituitary-axis related gene FKBP5 in combination with early life stress (ELA) on the structure of hippocampal subfields in MDD. 30986730 2019
dbSNP: rs1360780
rs1360780
Entrez Id: 2289;112267956
Gene Symbol: FKBP5;LOC112267956
FKBP5;LOC112267956
CUI: C0011581
Disease:
Depressive disorder
0.090 GeneticVariation BEFREE Clinical association to FKBP5 rs1360780 in patients with depression. 31219960 2019
dbSNP: rs1360780
rs1360780
Entrez Id: 2289;112267956
Gene Symbol: FKBP5;LOC112267956
FKBP5;LOC112267956
CUI: C0011570
Disease:
Mental Depression
0.080 GeneticVariation BEFREE The FKBP5 rs1360780 polymorphism is associated with plasma cortisol and FKBP5 mRNA expression after psychosocial stress in healthy controls but not in remitted depression. 25522420 2014
dbSNP: rs1360780
rs1360780
Entrez Id: 2289;112267956
Gene Symbol: FKBP5;LOC112267956
FKBP5;LOC112267956
CUI: C0344315
Disease:
Depressed mood
0.080 GeneticVariation BEFREE Clinical association to FKBP5 rs1360780 in patients with depression. 31219960 2019
dbSNP: rs1360780
rs1360780
Entrez Id: 2289;112267956
Gene Symbol: FKBP5;LOC112267956
FKBP5;LOC112267956
CUI: C0011570
Disease:
Mental Depression
0.080 GeneticVariation BEFREE Third, there is an additive interaction effect between FKBP5's rs1360780 variant and the graph-theoretical metrics of hippocampal connectivity to influence depression risk. 26801675 2017
dbSNP: rs1360780
rs1360780
Entrez Id: 2289;112267956
Gene Symbol: FKBP5;LOC112267956
FKBP5;LOC112267956
CUI: C0011570
Disease:
Mental Depression
0.080 GeneticVariation BEFREE Clinical association to FKBP5 rs1360780 in patients with depression. 31219960 2019
dbSNP: rs1360780
rs1360780
Entrez Id: 2289;112267956
Gene Symbol: FKBP5;LOC112267956
FKBP5;LOC112267956
CUI: C0011570
Disease:
Mental Depression
0.080 GeneticVariation BEFREE To investigate the possible relationship between genetic risk factors and depression in AD, we assessed genetic polymorphisms reported to be associated with depression (MAOA VNTR, ACE 288bp Insertion/ Deletion, 5HTTLPR, COMT Val158Met, BDNF Val66Met, TPH1 A218C, HTR2A T102C, P2RX7 Q460R, FKBP5 rs1360780 and CRHR1 rs242941) in a cross-sectional study on 246 AD patients with or without clinically significant major depressive disorder (MDD) according to DSM-IV. 23157339 2013
dbSNP: rs1360780
rs1360780
Entrez Id: 2289;112267956
Gene Symbol: FKBP5;LOC112267956
FKBP5;LOC112267956
CUI: C0011570
Disease:
Mental Depression
0.080 GeneticVariation BEFREE Given the large effect sizes, rs1360780 could be included into prediction models for depression in individuals exposed to childhood abuse. 21654733 2011
dbSNP: rs1360780
rs1360780
Entrez Id: 2289;112267956
Gene Symbol: FKBP5;LOC112267956
FKBP5;LOC112267956
CUI: C0011570
Disease:
Mental Depression
0.080 GeneticVariation BEFREE The significant interaction between ELA and the rs1360780 polymorphism in HATA suggests a role of FKBP5 in the pathophysiology of structural alterations in depression. 30986730 2019