Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 3953
Gene Symbol: LEPR
LEPR
0.400 GeneticVariation disease BEFREE Leptin receptor (LepR) deficiency is an autosomal-recessive endocrine disorder causing early-onset severe obesity, hyperphagia and pituitary hormone deficiencies. 31658438 2020
Entrez Id: 3952
Gene Symbol: LEP
LEP
0.400 Biomarker disease BEFREE SH2B1 is well-known as an adaptor protein, and deletion of SH2B1 results in severe obesity and both leptin and insulin resistance. 31739166 2020
Entrez Id: 3952
Gene Symbol: LEP
LEP
0.400 GeneticVariation disease BEFREE Congenital Leptin Deficiency and Leptin Gene Missense Mutation Found in Two Colombian Sisters with Severe Obesity. 31067764 2019
Entrez Id: 4160
Gene Symbol: MC4R
MC4R
0.400 AlteredExpression disease BEFREE Even a partial reduction in MC4R expression levels in mice, rats or humans produces hyperphagia and morbid obesity. 30561082 2019
Entrez Id: 3952
Gene Symbol: LEP
LEP
0.400 Biomarker disease BEFREE Circulating miRNAs showed significant association with plasma levels of adipokines; adiponectin, leptin, and L/A ratios in adolescents with severe obesity. 30309709 2019
Entrez Id: 3952
Gene Symbol: LEP
LEP
0.400 AlteredExpression disease BEFREE Leptin levels were higher in patients with severe obesity (p < 0.001). 31210052 2019
Entrez Id: 3952
Gene Symbol: LEP
LEP
0.400 Biomarker disease BEFREE University hospital, United States METHODS: Spexin, body mass index (BMI), insulin, glucose, total and high molecular weight adiponectin, leptin, and high sensitivity C- reactive protein were measured longitudinally (baseline, 6 mo, and 12 mo) after RYGB surgery in girls with severe obesity (n = 12; age = 16.7 ± 1.5 years; BMI = 51.6 ± 2.9 kg/m<sup>2</sup>). 30131311 2018
Entrez Id: 4160
Gene Symbol: MC4R
MC4R
0.400 GeneticVariation disease BEFREE Melanocortin receptor 4 (MC4R) is expressed in key brain regions, and MC4R gene mutations can cause severe obesity. 29501261 2018
Entrez Id: 4160
Gene Symbol: MC4R
MC4R
0.400 Biomarker disease BEFREE MC4R haploinsufficiency clearly segregates with higher BMI; however, severe obesity is not fully penetrant even in MC4R LOF carriers, suggesting critical roles for environmental and lifestyle factors in MC4R monogenic obesity. 29991773 2018
Entrez Id: 3953
Gene Symbol: LEPR
LEPR
0.400 GeneticVariation disease BEFREE While mouse models with deficient IL-6 signaling show an ameliorated but not absent Diethylnitrosamine (DEN)-induced HCC development, the morbid obesity in mice with mutant leptin signaling complicates the dissection of hepatic leptin receptor (LEPR) and IL-6 signaling in HCC development. 30224299 2018
Entrez Id: 3953
Gene Symbol: LEPR
LEPR
0.400 GeneticVariation disease BEFREE We identified a homozygous loss-of-function mutation, NM_002303.5:c.464 T > G; p.(Tyr155*), in the LEPR in an extended consanguineous family with multiple individuals affected by early-onset severe obesity and hyperphagia. 29545012 2018
Entrez Id: 4160
Gene Symbol: MC4R
MC4R
0.400 Biomarker disease BEFREE Genetic defects underlying the melanocortin-4 receptor (MC4R) signaling pathway lead to severe obesity. 29736023 2018
Entrez Id: 3953
Gene Symbol: LEPR
LEPR
0.400 GeneticVariation disease BEFREE Loss of function (LoF) mutations in the MC4R pathway, including mutations in the pro-opiomelanocortin (POMC), prohormone convertase 1 (PCSK1), leptin receptor (LEPR), or MC4R genes, have been shown to cause early-onset severe obesity. 29726959 2018
Entrez Id: 4160
Gene Symbol: MC4R
MC4R
0.400 GeneticVariation disease BEFREE Specifically, mutations in MC4R, the melanocortin-4 receptor gene, account for 3-5% of all severe obesity cases in humans<sup>1-3</sup>. 29311635 2018
Entrez Id: 4160
Gene Symbol: MC4R
MC4R
0.400 GeneticVariation disease BEFREE Analysis of the Impact of Common Polymorphisms of the FTO and MC4R Genes with the Risk of Severe Obesity in Saudi Arabian Population. 29466028 2018
Entrez Id: 4160
Gene Symbol: MC4R
MC4R
0.400 GeneticVariation disease BEFREE Loss of function (LoF) mutations in the MC4R pathway, including mutations in the pro-opiomelanocortin (POMC), prohormone convertase 1 (PCSK1), leptin receptor (LEPR), or MC4R genes, have been shown to cause early-onset severe obesity. 29726959 2018
Entrez Id: 4160
Gene Symbol: MC4R
MC4R
0.400 Biomarker disease CTD_human Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity. 29273807 2018
Entrez Id: 4160
Gene Symbol: MC4R
MC4R
0.400 Biomarker disease CTD_human Specifically, mutations in MC4R, the melanocortin-4 receptor gene, account for 3-5% of all severe obesity cases in humans<sup>1-3</sup>. 29311635 2018
Entrez Id: 3952
Gene Symbol: LEP
LEP
0.400 GeneticVariation disease BEFREE Early-onset severe obesity due to complete deletion of the leptin gene in a boy. 29040067 2017
Entrez Id: 4160
Gene Symbol: MC4R
MC4R
0.400 GeneticVariation disease BEFREE Mutations in the MC4R cause early-onset severe obesity. 28284973 2017
Entrez Id: 3953
Gene Symbol: LEPR
LEPR
0.400 GeneticVariation disease BEFREE In the present study we explored the association of six <i>LEPR</i> gene polymorphisms in patients with morbid obesity. 28096764 2016
Entrez Id: 3953
Gene Symbol: LEPR
LEPR
0.400 GeneticVariation disease BEFREE Novel Leptin Receptor Mutations Identified in Two Girls with Severe Obesity Are Associated with Increased Bone Mineral Density. 26925581 2016
Entrez Id: 3952
Gene Symbol: LEP
LEP
0.400 GeneticVariation disease BEFREE Leptin receptors belong to glycoprotein 130 (gp130) family of cytokine receptors and exist in six isoforms (LEPR a-f), and all the isoforms are encoded by LEPR gene; out of these isoforms, the LEPR-b receptor is the 'longest form,' and in most of the cases, mutations in this isoform cause severe obesity. 27313173 2016
Entrez Id: 3953
Gene Symbol: LEPR
LEPR
0.400 GeneticVariation disease BEFREE Leptin receptors belong to glycoprotein 130 (gp130) family of cytokine receptors and exist in six isoforms (LEPR a-f), and all the isoforms are encoded by LEPR gene; out of these isoforms, the LEPR-b receptor is the 'longest form,' and in most of the cases, mutations in this isoform cause severe obesity. 27313173 2016
Entrez Id: 4160
Gene Symbol: MC4R
MC4R
0.400 GeneticVariation disease BEFREE In conclusion, we have reported a novel mutation in MC4R in a family of Italian patients with severe obesity. 27706562 2016