TPH2, tryptophan hydroxylase 2, 121278

N. diseases: 137; N. variants: 37
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0233514
Disease: Abnormal behavior
Abnormal behavior
0.100 Biomarker phenotype BEFREE Evidence suggests that mice deficient in Tph2, the rate-limiting enzyme for brain serotonin synthesis, display disruptions in behavioral phenotypes relevant to stress-related psychiatric disorders. 31319134 2019
CUI: C0233514
Disease: Abnormal behavior
Abnormal behavior
0.100 GeneticVariation phenotype BEFREE Finally, we report on several association studies that have linked single nucleotide polymorphisms (SNPs) in the human TPH2 gene with behavioral disturbances and neuropsychiatric disorders. 30513372 2019
CUI: C0233514
Disease: Abnormal behavior
Abnormal behavior
0.100 Biomarker phenotype BEFREE This dual role of TPH2 should be taken into consideration during therapy of psychiatric disorders. 31216212 2019
CUI: C0233514
Disease: Abnormal behavior
Abnormal behavior
0.100 GeneticVariation phenotype BEFREE Characterizing how exactly the different TPH2 variants influence the serotonergic neurotransmission is a next necessary step in understanding the psychiatric disorders where serotonin is implicated. 29775696 2018
CUI: C0233514
Disease: Abnormal behavior
Abnormal behavior
0.100 GeneticVariation phenotype BEFREE We examined whether the TPH2 polymorphism -703G/T (rs4570625) is associated with aggressiveness and impulsivity, and the prevalence of psychiatric disorders, in a population-representative sample. 28342337 2017
CUI: C0233514
Disease: Abnormal behavior
Abnormal behavior
0.100 GeneticVariation phenotype BEFREE Four single nucleotide polymorphisms (SNPs) in the TPH1 gene and one SNP in the TPH2 gene were selected based on previous studies investigating associations between these SNPs and psychiatric or behavioral disorders. 23172723 2014
CUI: C0233514
Disease: Abnormal behavior
Abnormal behavior
0.100 GeneticVariation phenotype BEFREE These findings suggest that the association of risk for psychiatric disorders with a common TPH2 yin haplotype is related to the inefficient functional engagement of cortical areas involved in cognitive control and alterations in the mode of functional connectivity of dACC pathways. 22915309 2012
CUI: C0233514
Disease: Abnormal behavior
Abnormal behavior
0.100 Biomarker phenotype BEFREE The gene for tryptophan hydroxylase 2, which is a rate limiting enzyme in serotonin synthesis, is considered an important candidate gene associated with psychiatric disorders. 21829912 2011
CUI: C0233514
Disease: Abnormal behavior
Abnormal behavior
0.100 GeneticVariation phenotype BEFREE Risk-taking behavior in a gambling task associated with variations in the tryptophan hydroxylase 2 gene: relevance to psychiatric disorders. 20043001 2010
CUI: C0233514
Disease: Abnormal behavior
Abnormal behavior
0.100 Biomarker phenotype BEFREE Tryptophan hydroxylase 2 (TPH2) which is a rate limiting enzyme in the serotonin synthesis is considered an important candidate gene associated with psychiatric disorders. 19800079 2010
CUI: C0233514
Disease: Abnormal behavior
Abnormal behavior
0.100 Biomarker phenotype BEFREE Although the predominant role of tryptophan hydroxylase 2 (TPH2) in the CNS and its influence on the vulnerability to psychiatric disorders have clearly been demonstrated in several studies, the role of TPH1 on neuronal mechanisms, respectively on behavioral traits is still poorly understood. 19233335 2009
CUI: C0233514
Disease: Abnormal behavior
Abnormal behavior
0.100 Biomarker phenotype BEFREE The rate-limiting enzyme of serotonin biosynthesis, tryptophan hydroxylase 2 (TPH2), is one of the most promising candidate genes for psychiatric disorders. 19588223 2009
CUI: C0233514
Disease: Abnormal behavior
Abnormal behavior
0.100 Biomarker phenotype BEFREE Sixteen TPH2 SNPs were genotyped in a Romanian sample of 198 BPI patients and 180 controls screened for psychiatric disorders. 18797398 2008
CUI: C0233514
Disease: Abnormal behavior
Abnormal behavior
0.100 GeneticVariation phenotype BEFREE Expression of mutant Tph2 in mice results in markedly reduced ( approximately 80%) brain 5-HT production and leads to behavioral abnormalities in tests assessing 5-HT-mediated emotional states. 18212115 2008
CUI: C0233514
Disease: Abnormal behavior
Abnormal behavior
0.100 GeneticVariation phenotype BEFREE Despite reports of possible associations between polymorphisms in human TPH2 and many psychiatric disorders, including bipolar disorder (BPD), the functional effect and susceptibility loci of such polymorphisms for BPD have not yet been identified. 17768266 2007
CUI: C0233514
Disease: Abnormal behavior
Abnormal behavior
0.100 AlteredExpression phenotype BEFREE Tryptophan hydroxylase 2 (TPH2) was found to be solely expressed in the brain and therefore considered an important susceptibility gene in psychiatric disorders. 17015812 2006
CUI: C0233514
Disease: Abnormal behavior
Abnormal behavior
0.100 Biomarker phenotype BEFREE The novel tryptophan hydroxylase isoform (TPH2), being the rate-limiting enzyme in the biosynthesis of serotonin, has many biological functions and plays an important role as candidate gene in several psychiatric disorders. 17011525 2006