TSPO, translocator protein, 706

N. diseases: 8; N. variants: 2
Source: CURATED ×
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0005586
Disease: Bipolar Disorder
Bipolar Disorder 		0.330 Biomarker disease PSYGENET We report a nominal association between this TSPO polymorphism and the diagnosis of Bipolar Disorder in both the genome-wide dataset of the Wellcome Trust Case-Control Consortium and the Psychiatric Genome-Wide Association Study Consortium Bipolar Disorder group (OR=1.11, p=0.007; OR=1.10, p=0.011, respectively). 23942012 2013
CUI: C0745744
Disease: End Stage Liver Disease
End Stage Liver Disease 		0.310 Biomarker disease CTD_human Pathogenesis of hepatic encephalopathy: update on molecular mechanisms. 15025246 2003
CUI: C2936476
Disease: Chronic Liver Failure
Chronic Liver Failure 		0.310 Biomarker disease CTD_human Pathogenesis of hepatic encephalopathy: update on molecular mechanisms. 15025246 2003
CUI: C0023893
Disease: Liver Cirrhosis, Experimental
Liver Cirrhosis, Experimental 		0.300 Biomarker disease CTD_human Systems level analysis and identification of pathways and networks associated with liver fibrosis. 25380136 2014
CUI: C0019147
Disease: Hepatic Coma
Hepatic Coma 		0.300 Biomarker disease CTD_human Hepatic encephalopathy: An update of pathophysiologic mechanisms. 10564534 1999
CUI: C0019151
Disease: Hepatic Encephalopathy
Hepatic Encephalopathy 		0.300 Biomarker disease CTD_human Hepatic encephalopathy: An update of pathophysiologic mechanisms. 10564534 1999
CUI: C0751197
Disease: Fulminant Hepatic Failure with Cerebral Edema
Fulminant Hepatic Failure with Cerebral Edema 		0.300 Biomarker disease CTD_human Hepatic encephalopathy: An update of pathophysiologic mechanisms. 10564534 1999
CUI: C0751198
Disease: Hepatic Stupor
Hepatic Stupor 		0.300 Biomarker disease CTD_human Hepatic encephalopathy: An update of pathophysiologic mechanisms. 10564534 1999
CUI: C0019147
Disease: Hepatic Coma
Hepatic Coma 		0.300 Biomarker disease CTD_human Alterations of neurotransmitter-related gene expression in human and experimental portal-systemic encephalopathy. 10206825 1998
CUI: C0019151
Disease: Hepatic Encephalopathy
Hepatic Encephalopathy 		0.300 Biomarker disease CTD_human Alterations of neurotransmitter-related gene expression in human and experimental portal-systemic encephalopathy. 10206825 1998
CUI: C0751197
Disease: Fulminant Hepatic Failure with Cerebral Edema
Fulminant Hepatic Failure with Cerebral Edema 		0.300 Biomarker disease CTD_human Alterations of neurotransmitter-related gene expression in human and experimental portal-systemic encephalopathy. 10206825 1998
CUI: C0751198
Disease: Hepatic Stupor
Hepatic Stupor 		0.300 Biomarker disease CTD_human Alterations of neurotransmitter-related gene expression in human and experimental portal-systemic encephalopathy. 10206825 1998