Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0005586
Disease: Bipolar Disorder
Bipolar Disorder
0.330 GeneticVariation disease BEFREE The current study aimed to investigate the relationships between genetic variants in NR1D1 RORA, and RORB genes and BD in the Han Chinese population. 25789810 2015
CUI: C0005586
Disease: Bipolar Disorder
Bipolar Disorder
0.330 Biomarker disease PSYGENET Several circadian genes have been found to be associated with bipolar disorders: at least three studies have reported positive associations for each of CLOCK, NPAS2, ARNTL1, NR1D1, PER3, RORB and CSNK1epsilon. 24389266 2014
CUI: C0005586
Disease: Bipolar Disorder
Bipolar Disorder
0.330 Biomarker disease PSYGENET The findings that have gained support indicate that genetic variants of RORA (rs2028122) and CRY1 (rs2287161) associate with depressive disorder, those of RORB (rs7022435, rs3750420, rs1157358, rs3903529) and NR1D1 (rs2314339) with bipolar disorder, and those of NPAS2 (rs11541353) and CRY2 (rs10838524) with seasonal affective disorder or winter depression. 22538398 2012
CUI: C0005586
Disease: Bipolar Disorder
Bipolar Disorder
0.330 GeneticVariation disease BEFREE The findings that have gained support indicate that genetic variants of RORA (rs2028122) and CRY1 (rs2287161) associate with depressive disorder, those of RORB (rs7022435, rs3750420, rs1157358, rs3903529) and NR1D1 (rs2314339) with bipolar disorder, and those of NPAS2 (rs11541353) and CRY2 (rs10838524) with seasonal affective disorder or winter depression. 22538398 2012
CUI: C0005586
Disease: Bipolar Disorder
Bipolar Disorder
0.330 Biomarker disease PSYGENET Such connections to circadian genes such as CLOCK, ARNTL1, NPAS2, PER3 and NR1D1 have been repeatedly demonstrated for bipolar disorders, and to a lesser extent for recurrent depressive disorders and seasonal affective disorders. 21835597 2011
CUI: C0005586
Disease: Bipolar Disorder
Bipolar Disorder
0.330 Biomarker disease PSYGENET Using lymphoblastoid cell lines from patients with BD, we found that both the NR1D1 and GSK3β variants are associated with functional differences in gene expression. 21781277 2011
CUI: C0005586
Disease: Bipolar Disorder
Bipolar Disorder
0.330 Biomarker disease PSYGENET We examined 209 single-nucleotide polymorphisms (SNPs) covering 19 circadian genes (ADCYAP1, ARNTL, ARNTL2, BHLHB2, BHLHB3, CLOCK, CRY1, CRY2, CSNK1E, DBP, NPAS2, NR1D1, PER1, PER2, PER3, RORA, TIMELESS, VIP, and VIPR2) in a sample of 534 MD patients (335 with unipolar major mood depression (MDD) and 199 with bipolar disorder (BD)) and 440 community-based screened controls. 20072116 2010
CUI: C0005586
Disease: Bipolar Disorder
Bipolar Disorder
0.330 GeneticVariation disease BEFREE The aim of our study was to investigate the association between REV-ERBalpha gene (NR1D1) single nucleotide polymorphisms (SNPs) and bipolar disorder (BP) in a case-control sample of Sardinian ancestry and evaluate its effect on age at onset (AAO) of BP. 19267705 2009
CUI: C0011581
Disease: Depressive disorder
Depressive disorder
0.320 Biomarker disease BEFREE The Per1 and Nr1d1 profiles were advanced in patients in mania compared with those in depression. 25359533 2015
CUI: C0011581
Disease: Depressive disorder
Depressive disorder
0.320 Biomarker disease PSYGENET The findings that have gained support indicate that genetic variants of RORA (rs2028122) and CRY1 (rs2287161) associate with depressive disorder, those of RORB (rs7022435, rs3750420, rs1157358, rs3903529) and NR1D1 (rs2314339) with bipolar disorder, and those of NPAS2 (rs11541353) and CRY2 (rs10838524) with seasonal affective disorder or winter depression. 22538398 2012
CUI: C0011581
Disease: Depressive disorder
Depressive disorder
0.320 GeneticVariation disease BEFREE The findings that have gained support indicate that genetic variants of RORA (rs2028122) and CRY1 (rs2287161) associate with depressive disorder, those of RORB (rs7022435, rs3750420, rs1157358, rs3903529) and NR1D1 (rs2314339) with bipolar disorder, and those of NPAS2 (rs11541353) and CRY2 (rs10838524) with seasonal affective disorder or winter depression. 22538398 2012
CUI: C0085159
Disease: Seasonal Affective Disorder
Seasonal Affective Disorder
0.320 GeneticVariation disease BEFREE The findings that have gained support indicate that genetic variants of RORA (rs2028122) and CRY1 (rs2287161) associate with depressive disorder, those of RORB (rs7022435, rs3750420, rs1157358, rs3903529) and NR1D1 (rs2314339) with bipolar disorder, and those of NPAS2 (rs11541353) and CRY2 (rs10838524) with seasonal affective disorder or winter depression. 22538398 2012
CUI: C0085159
Disease: Seasonal Affective Disorder
Seasonal Affective Disorder
0.320 Biomarker disease PSYGENET The findings that have gained support indicate that genetic variants of RORA (rs2028122) and CRY1 (rs2287161) associate with depressive disorder, those of RORB (rs7022435, rs3750420, rs1157358, rs3903529) and NR1D1 (rs2314339) with bipolar disorder, and those of NPAS2 (rs11541353) and CRY2 (rs10838524) with seasonal affective disorder or winter depression. 22538398 2012
CUI: C0085159
Disease: Seasonal Affective Disorder
Seasonal Affective Disorder
0.320 Biomarker disease BEFREE Such connections to circadian genes such as CLOCK, ARNTL1, NPAS2, PER3 and NR1D1 have been repeatedly demonstrated for bipolar disorders, and to a lesser extent for recurrent depressive disorders and seasonal affective disorders. 21835597 2011
CUI: C0085159
Disease: Seasonal Affective Disorder
Seasonal Affective Disorder
0.320 Biomarker disease PSYGENET Such connections to circadian genes such as CLOCK, ARNTL1, NPAS2, PER3 and NR1D1 have been repeatedly demonstrated for bipolar disorders, and to a lesser extent for recurrent depressive disorders and seasonal affective disorders. 21835597 2011
CUI: C0015695
Disease: Fatty Liver
Fatty Liver
0.300 Biomarker disease CTD_human REV-ERBα Activates C/EBP Homologous Protein to Control Small Heterodimer Partner-Mediated Oscillation of Alcoholic Fatty Liver. 27664470 2016
CUI: C2711227
Disease: Steatohepatitis
Steatohepatitis
0.300 Biomarker disease CTD_human REV-ERBα Activates C/EBP Homologous Protein to Control Small Heterodimer Partner-Mediated Oscillation of Alcoholic Fatty Liver. 27664470 2016
CUI: C0020676
Disease: Hypothyroidism
Hypothyroidism
0.230 AlteredExpression disease BEFREE Hypothyroidism disrupted the circadian expression pattern of Bmal1 and period circadian regulator 2 (Per2) and decreased the mesor of Nr1d1 and Tef. 30747053 2019
CUI: C0020676
Disease: Hypothyroidism
Hypothyroidism
0.230 AlteredExpression disease BEFREE Regarding the modulation of gene expression in the testis, hypothyroidism increased the expression of Thra1 and decreased the expression of Dio3, and hyperthyroidism increased the expression of Slc16a2. 27066791 2017
CUI: C0020676
Disease: Hypothyroidism
Hypothyroidism
0.230 GeneticVariation disease BEFREE Hypothyroidism due to THRA1 (gene coding for thyroid hormone receptor α1) mutation-mediated Resistance to Thyroid Hormone (RTH) has been recently reported in human and is associated with memory deficits similar to those found in a mouse model for Thra1 mutation mediated RTH (Thra1(+/m) mice). 26743578 2016
CUI: C0020676
Disease: Hypothyroidism
Hypothyroidism
0.230 Biomarker disease RGD Developmental expression of mRNAs from a rat C-erbA genomic locus. 1315530 1992
CUI: C0020550
Disease: Hyperthyroidism
Hyperthyroidism
0.220 AlteredExpression disease BEFREE Hyperthyroidism increased the mRNA expression of core clock genes and thyrotrophic embryonic factor (Tef), as well as the mesor and amplitude of brain and muscle Arnt-like protein-1 (Bmal1) and the mesor of nuclear receptor subfamily 1 (Nr1d1) group D member 1, when compared to euthyroid animals. 30747053 2019
CUI: C0020550
Disease: Hyperthyroidism
Hyperthyroidism
0.220 AlteredExpression disease BEFREE Regarding the modulation of gene expression in the testis, hypothyroidism increased the expression of Thra1 and decreased the expression of Dio3, and hyperthyroidism increased the expression of Slc16a2. 27066791 2017
CUI: C0020550
Disease: Hyperthyroidism
Hyperthyroidism
0.220 Biomarker disease RGD Developmental expression of mRNAs from a rat C-erbA genomic locus. 1315530 1992
Diabetes Mellitus, Non-Insulin-Dependent
0.210 Biomarker disease BEFREE HPM display robust circadian rhythms in clock genes, but REVERBA displayed dampened rhythmicity in type 2 diabetes. 27756900 2016