MTNR1B, melatonin receptor 1B, 4544

N. diseases: 93; N. variants: 11
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X
0.030 Biomarker disease BEFREE However, an association between the MTNR1B gene and IR/hypercholesterolemia/metabolic syndrome was observed in obese adolescents. 29726288 2018
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X
0.030 GeneticVariation disease BEFREE In addition, genetic variants of BCL11A, GCKR, ADAMTS9, CDKAL1, KLF14, CDKN2BAS, TCF7L2, CDC123/CAMK1D, HHEX, MTNR1B, and KCNQ1 contributed to the risk for T2D without MetS (P < 0.05). 26599349 2015
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X
0.030 GeneticVariation disease BEFREE The aim of this study was to assess the effects of MTNR1B variants on traits related to the metabolic syndrome in the self-contained population of Sorbs from Germany. 21711391 2011