TPH2, tryptophan hydroxylase 2, 121278

N. diseases: 137; N. variants: 37
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs120074176
rs120074176
Entrez Id: 121278
Gene Symbol: TPH2
TPH2
CUI: C2751802
Disease:
ATTENTION DEFICIT-HYPERACTIVITY DISORDER, SUSCEPTIBILITY TO, 7
0.800 GeneticVariation UNIPROT A loss-of-function mutation in tryptophan hydroxylase 2 segregating with attention-deficit/hyperactivity disorder. 18347598 2008
dbSNP: rs120074176
rs120074176
Entrez Id: 121278
Gene Symbol: TPH2
TPH2
CUI: C2751802
Disease:
ATTENTION DEFICIT-HYPERACTIVITY DISORDER, SUSCEPTIBILITY TO, 7
T 0.800 SusceptibilityMutation CLINVAR
dbSNP: rs17110563
rs17110563
Entrez Id: 121278
Gene Symbol: TPH2
TPH2
CUI: C1445957
Disease:
Serum total cholesterol measurement
0.700 GeneticVariation GWASDB Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci. 23063622 2012
dbSNP: rs120074175
rs120074175
Entrez Id: 121278
Gene Symbol: TPH2
TPH2
CUI: C4017088
Disease:
UNIPOLAR DEPRESSION, SUSCEPTIBILITY TO
A 0.700 SusceptibilityMutation CLINVAR
dbSNP: rs17110563
rs17110563
Entrez Id: 121278
Gene Symbol: TPH2
TPH2
CUI: C1862077
Disease:
BIPOLAR AFFECTIVE DISORDER, SUSCEPTIBILITY TO
T 0.700 SusceptibilityMutation CLINVAR
dbSNP: rs11178997
rs11178997
Entrez Id: 121278
Gene Symbol: TPH2
TPH2
CUI: C0038436
Disease:
Post-Traumatic Stress Disorder
0.030 GeneticVariation BEFREE No association was found for the TPH2 SNPs rs11178997 and rs1386494 in relation to PTSD or comorbid psychopathology. 31291234 2019
dbSNP: rs4570625
rs4570625
Entrez Id: 121278
Gene Symbol: TPH2
TPH2
CUI: C1269683
Disease:
Major Depressive Disorder
0.030 GeneticVariation BEFREE They aimed to investigate the alterations in the cortical gyrification of the prefrontal cortex and anterior cingulate cortex and their association with the TPH2 rs4570625 polymorphism in patients with MDD. 27807918 2017
dbSNP: rs120074175
rs120074175
Entrez Id: 121278
Gene Symbol: TPH2
TPH2
CUI: C1269683
Disease:
Major Depressive Disorder
0.030 GeneticVariation BEFREE Chinese Han individuals with at least one rs11178997 T allele or rs120074175 A allele are susceptible to MD even in the relative absence of high-negative life events. 26386440 2015
dbSNP: rs120074175
rs120074175
Entrez Id: 121278
Gene Symbol: TPH2
TPH2
CUI: C0041696
Disease:
Unipolar Depression
0.030 GeneticVariation BEFREE Chinese Han individuals with at least one rs11178997 T allele or rs120074175 A allele are susceptible to MD even in the relative absence of high-negative life events. 26386440 2015
dbSNP: rs4570625
rs4570625
Entrez Id: 121278
Gene Symbol: TPH2
TPH2
CUI: C1269683
Disease:
Major Depressive Disorder
0.030 GeneticVariation BEFREE Individuals carrying the T(-) genotype of rs4570625 (GG), T(-) genotype of rs11178997 (AA), or A(-) genotype of rs120074175 (GG) were susceptible to MD only when exposed to high-negative life events. 26386440 2015
dbSNP: rs11178997
rs11178997
Entrez Id: 121278
Gene Symbol: TPH2
TPH2
CUI: C0038436
Disease:
Post-Traumatic Stress Disorder
0.030 GeneticVariation BEFREE The results indicated that, although the rs11178997 genotype was not associated with total PTSD symptoms, it could significantly predict severity of PTSD's avoidance symptoms in women. 25014617 2014
dbSNP: rs11178997
rs11178997
Entrez Id: 121278
Gene Symbol: TPH2
TPH2
CUI: C0038436
Disease:
Post-Traumatic Stress Disorder
0.030 GeneticVariation BEFREE Also, there was a significant association of PTSD symptoms and the 't' allele of TPH2 SNP rs11178997 (p=0.03), explaining 4% of the variance. 22483952 2012
dbSNP: rs4570625
rs4570625
Entrez Id: 121278
Gene Symbol: TPH2
TPH2
CUI: C1269683
Disease:
Major Depressive Disorder
0.030 GeneticVariation BEFREE The synthesis of the data shown that two SNPs (rs4570625 and rs17110747) were associated with MDD using fixed effects models. 22693556 2012
dbSNP: rs120074175
rs120074175
Entrez Id: 121278
Gene Symbol: TPH2
TPH2
CUI: C1269683
Disease:
Major Depressive Disorder
0.030 GeneticVariation BEFREE This mutant is equivalent to a rare human variant (R441H) identified in few individuals with unipolar major depression. 18212115 2008
dbSNP: rs120074175
rs120074175
Entrez Id: 121278
Gene Symbol: TPH2
TPH2
CUI: C0041696
Disease:
Unipolar Depression
0.030 GeneticVariation BEFREE This mutant is equivalent to a rare human variant (R441H) identified in few individuals with unipolar major depression. 18212115 2008
dbSNP: rs120074175
rs120074175
Entrez Id: 121278
Gene Symbol: TPH2
TPH2
CUI: C0041696
Disease:
Unipolar Depression
0.030 GeneticVariation BEFREE It was recently reported that a rare functional variant, R441H, in the human tryptophan hydroxylase-2 gene (hTPH2) could represent an important risk factor for unipolar major depression (UP) since it was originally found in 10% of UP patients (vs. 1.4% in control subjects). 16581035 2006
dbSNP: rs120074175
rs120074175
Entrez Id: 121278
Gene Symbol: TPH2
TPH2
CUI: C1269683
Disease:
Major Depressive Disorder
0.030 GeneticVariation BEFREE It was recently reported that a rare functional variant, R441H, in the human tryptophan hydroxylase-2 gene (hTPH2) could represent an important risk factor for unipolar major depression (UP) since it was originally found in 10% of UP patients (vs. 1.4% in control subjects). 16581035 2006
dbSNP: rs4290270
rs4290270
Entrez Id: 121278
Gene Symbol: TPH2
TPH2
CUI: C1269683
Disease:
Major Depressive Disorder
0.020 GeneticVariation BEFREE Hence, rs4290270 could potentially serve as a reliable biomarker to identify MDD patients with early wakening symptom. 30519155 2018
dbSNP: rs4290270
rs4290270
Entrez Id: 121278
Gene Symbol: TPH2
TPH2
CUI: C1269683
Disease:
Major Depressive Disorder
0.020 GeneticVariation BEFREE TPH2 rs4290270 was genotyped in 165 suicide attempters and 188 suicide non-attempters diagnosed with major depressive disorder, bipolar disorder and schizophrenia. 28084537 2017
dbSNP: rs4570625
rs4570625
Entrez Id: 121278
Gene Symbol: TPH2
TPH2
CUI: C0860603
Disease:
Anxiety symptoms
0.020 GeneticVariation BEFREE TPH2 rs4570625 GG carriers were more likely to achieve depressive and anxiety symptom remission compared with T-allele carriers. 26745768 2016
dbSNP: rs4570625
rs4570625
Entrez Id: 121278
Gene Symbol: TPH2
TPH2
CUI: C0003467
Disease:
Anxiety
0.020 GeneticVariation BEFREE Exploratory analysis of genotypes in currently dependent patients showed that rs1843809 was associated with depressive and aggressive traits (p=0.045 and p=0.001, respectively), rs4290270 with depressive and anxiety traits (p=0.040 and p=0.025, respectively) and rs4570625 with aggressive traits (p=0.011). 26232682 2015
dbSNP: rs4570625
rs4570625
Entrez Id: 121278
Gene Symbol: TPH2
TPH2
CUI: C0003469
Disease:
Anxiety Disorders
0.020 GeneticVariation BEFREE Exploratory analysis of genotypes in currently dependent patients showed that rs1843809 was associated with depressive and aggressive traits (p=0.045 and p=0.001, respectively), rs4290270 with depressive and anxiety traits (p=0.040 and p=0.025, respectively) and rs4570625 with aggressive traits (p=0.011). 26232682 2015
dbSNP: rs7305115
rs7305115
Entrez Id: 121278
Gene Symbol: TPH2
TPH2
CUI: C0011581
Disease:
Depressive disorder
0.020 GeneticVariation BEFREE There was a significant interactive effect of rs7305115 polymorphisms and depression diagnosis on Symbol Digit Modalities Test (SDMT) (P<0.05). 26057341 2015
dbSNP: rs7305115
rs7305115
Entrez Id: 121278
Gene Symbol: TPH2
TPH2
CUI: C0011581
Disease:
Depressive disorder
0.020 GeneticVariation BEFREE We hypothesize that functional polymorphisms (TPH2: rs7305115, 5-HTTLPR and rs25531) within both genes contribute to the risk of depressive disorders after childhood abuse in adult life. 25214390 2014
dbSNP: rs1473473
rs1473473
Entrez Id: 121278
Gene Symbol: TPH2
TPH2
CUI: C0232600
Disease:
Self-induced vomiting
0.020 GeneticVariation BEFREE TPH2 (tryptophan hydroxylase 2) SNP rs1473473 was previously associated with anorexia nervosa and EDs characterized by SV. 23239044 2013