Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 8431
Gene Symbol: NR0B2
NR0B2
0.690 AlteredExpression disease BEFREE Therefore, in addition to the previous findings of SBM on obesity here we show an additional mechanism which by changing the expression of genes involved in lipid metabolism via the PPARG/SHP pathway in the liver. 31707284 2020
Entrez Id: 8431
Gene Symbol: NR0B2
NR0B2
0.690 Biomarker disease BEFREE Nuclear receptor subfamily 0, group B, member 2 may play a role in obesity and insulin resistance in patients with PCOS. 24517280 2014
Entrez Id: 8431
Gene Symbol: NR0B2
NR0B2
0.690 GeneticVariation disease BEFREE Mutations of the small heterodimer partner (SHP) gene have been associated with mild obesity in Japanese subjects. 20233523 2010
Entrez Id: 8431
Gene Symbol: NR0B2
NR0B2
0.690 GeneticVariation disease BEFREE SHP mutations may also be associated with later obesity and insulin resistance syndrome that induces diabetes. 18781616 2008
Entrez Id: 8431
Gene Symbol: NR0B2
NR0B2
0.690 AlteredExpression disease BEFREE Mice lacking SHP show increased basal expression of PGC-1alpha, increased energy expenditure, and resistance to diet-induced obesity. 16213225 2005
Entrez Id: 8431
Gene Symbol: NR0B2
NR0B2
0.690 GeneticVariation disease BEFREE Using combined SSCP and heteroduplex analysis, we analyzed the entire coding region of SHP for variants in a cohort of 750 Danish men with early-onset obesity and genotyped a cohort of 795 nonobese control subjects using PCR-RFLP. 15459958 2004
Entrez Id: 8431
Gene Symbol: NR0B2
NR0B2
0.690 GeneticVariation disease BEFREE The coding regions and 562 bases of the SHP promoter were screened for mutations in 329 subjects with severe early-onset obesity. 12716767 2003
Entrez Id: 8431
Gene Symbol: NR0B2
NR0B2
0.690 GeneticVariation disease BEFREE Because mutations in human SHP1 underlie obesity and diabetes, SHP1 is a candidate gene for human lipodystrophy syndromes. 12181644 2002
Entrez Id: 8431
Gene Symbol: NR0B2
NR0B2
0.690 GeneticVariation disease BEFREE Interestingly, all of the subjects with the mutations were mildly or moderately obese at onset of diabetes, and analysis of the lineages of these individuals indicated that the SHP mutations were associated with obesity rather than with diabetes. 11136233 2001
Entrez Id: 8431
Gene Symbol: NR0B2
NR0B2
0.690 Biomarker disease HPO
Entrez Id: 8431
Gene Symbol: NR0B2
NR0B2
0.690 Biomarker disease GENOMICS_ENGLAND
Entrez Id: 8431
Gene Symbol: NR0B2
NR0B2
0.690 Biomarker disease CTD_human