Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 3952
Gene Symbol: LEP
LEP
0.700 GeneticVariation disease BEFREE Obesity as measured by body mass index (BMI) is associated with risk of several cancers and has also been suggested as a risk factor for CM, and may also be related to insufficient 25(OH)D and/or high leptin levels. 28637727 2017
Entrez Id: 3952
Gene Symbol: LEP
LEP
0.700 GeneticVariation disease BEFREE Loss of neuropeptide Y (NPY) can correct the obesity syndrome of mutant mice lacking of leptin (ob/ob). 28864114 2017
Entrez Id: 3952
Gene Symbol: LEP
LEP
0.700 GeneticVariation disease BEFREE Gender-specific effect of Pro12Ala polymorphism in peroxisome proliferator-activated receptor gamma-2 gene on obesity risk and leptin levels in a Tunisian population. 19733160 2009
Entrez Id: 3952
Gene Symbol: LEP
LEP
0.700 GeneticVariation disease BEFREE Rare, non-syndromic forms of obesity are a result of loss-of-function mutations in genes that act on the development and function of the hypothalamus or the leptin-melanocortin pathway. 28735903 2017
Entrez Id: 3952
Gene Symbol: LEP
LEP
0.700 GeneticVariation disease BEFREE Here, we show that Lgr4 homozygous mutant (Lgr4(m/m)) mice show reduced adiposity and resist dietary and leptin mutant-induced obesity with improved glucose metabolism. 24212090 2013
Entrez Id: 3952
Gene Symbol: LEP
LEP
0.700 GeneticVariation disease BEFREE The subjects carrying Gly16 or Glu27 alleles regardless of BMI had greater total fat mass, W/H and plasma leptin compared with those without the Gly16 or Glu27 alleles, indicating that Gly16 and Glu27 alleles of the beta2-adrenoceptor gene are related to obesity and fat mass. 17027833 2006
Entrez Id: 3952
Gene Symbol: LEP
LEP
0.700 GeneticVariation disease BEFREE The Lim domain homeobox gene (Isl-1) is a positional candidate gene for obesity that maps on chromosome 5q11-q13, a locus linked to BMI and leptin levels in French Caucasians. 11978668 2002
Entrez Id: 3952
Gene Symbol: LEP
LEP
0.700 GeneticVariation disease BEFREE We searched the PubMed, Web of Science, and China National Knowledge Infrastructure databases for studies that evaluated the association between LEP G-2548A polymorphisms and obesity risk prior to March 2014. 25733497 2016
Entrez Id: 3952
Gene Symbol: LEP
LEP
0.700 GeneticVariation disease BEFREE The aim of this study was to investigate the association of leptin receptor gene Q223R polymorphism on obesity in association with body mass index (BMI), lipid parameters, plasma leptin levels and homeostasis model assessment of insulin resistance (HOMA-IR). 23954230 2013
Entrez Id: 3952
Gene Symbol: LEP
LEP
0.700 GeneticVariation disease BEFREE The findings suggest that the leptin promoter G-2548A variant may play its part in the progression to obesity by not only affecting the body's fat distribution but also by changing the serum leptin and HDLC levels. 27240985 2016
Entrez Id: 3952
Gene Symbol: LEP
LEP
0.700 GeneticVariation disease BEFREE This study suggests that shorter sleep duration in children from China (< 8h/day), compared to longer sleep duration (≥10 h/day), has a long-term impact on the association of polygenic risk for obesity from childhood to young adulthood and leptin pathway explains a key mechanism via a modification effect. 31285522 2019
Entrez Id: 3952
Gene Symbol: LEP
LEP
0.700 GeneticVariation disease BEFREE The aim of the present study was to evaluate the relationship between oligopolymorphism in the 25th codon of leptin gene and obesity. 25117807 2014
Entrez Id: 3952
Gene Symbol: LEP
LEP
0.700 GeneticVariation disease BEFREE Genes currently recognized to be involved include KAL-1 (associated with X-linked Kallmann Syndrome), gonadotropin-releasing hormone (GnRH) receptor, gonadotropins, pituitary transcription factors (HESX1, LHX3, and PROP-1), orphan nuclear receptors (DAX-1, associated with X-linked adrenal hypoplasia congenital, and SF-1), and three genes also associated with obesity (leptin, leptin receptor, and prohormone convertase 1 [ PC1]). 12536356 2002
Entrez Id: 3952
Gene Symbol: LEP
LEP
0.700 GeneticVariation disease BEFREE Therefore, the present study aimed to evaluate the relationships among the gene polymorphisms ghrelin (GHRL-rs26802), ghrelin receptor (GHSR-rs572169), leptin (LEP-rs7799039), leptin receptor (LEPR-rs1137101) and fat mass and obesity-associated (FTO-rs9939609) and obesity. 26255942 2015
Entrez Id: 3952
Gene Symbol: LEP
LEP
0.700 GeneticVariation disease BEFREE The objective of our study was to determine whether the LEPR Q223R polymorphism and the LEP promoter 2548G/A polymorphism are associated with obesity in a group of male and female patients using atypical antipsychotic drugs. 19142102 2009
Entrez Id: 3952
Gene Symbol: LEP
LEP
0.700 GeneticVariation disease BEFREE These results suggest that variation within the LEP and MC4R genes is associated with reduced risk for obesity in females. 17587397 2007
Entrez Id: 3952
Gene Symbol: LEP
LEP
0.700 GeneticVariation disease BEFREE Carrying a minor allele of the nonsynonymous SNP rs6971091 conferred an odds ratio of at least 2 for obesity defined by both BMI and leptin levels. 18317470 2008
Entrez Id: 3952
Gene Symbol: LEP
LEP
0.700 GeneticVariation disease BEFREE We have previously shown that early weaning in rats increases the risk of obesity and insulin resistance at adulthood, and leptin resistance can be a prime factor leading to these changes. 24956416 2014
Entrez Id: 3952
Gene Symbol: LEP
LEP
0.700 GeneticVariation disease BEFREE The ADRbeta3 variant was not significantly associated with any of the obesity-related traits, but subjects with the PPAR-gamma2 variant (n = 98) had significantly higher levels of lasting insulin (P = 0.03), leptin (P = 0.009), and waist circumference (P = 0.03) than those without. 11315829 2001
Entrez Id: 3952
Gene Symbol: LEP
LEP
0.700 GeneticVariation disease BEFREE Class I/I genotypes of leptin showed significantly high risk for developing hypertension irrespective of obesity. 24171506 2014
Entrez Id: 3952
Gene Symbol: LEP
LEP
0.700 GeneticVariation disease BEFREE Association of rs9939609 variant with higher FBG, plasma insulin, and leptin levels indicates that this polymorphism may disturb the metabolism in adult females and predispose them to obesity and type 2 diabetes. 24102053 2013
Entrez Id: 3952
Gene Symbol: LEP
LEP
0.700 GeneticVariation disease BEFREE In humans, leptin deficiency due to a mutation in the leptin gene is associated with early-onset obesity. 9537324 1998
Entrez Id: 3952
Gene Symbol: LEP
LEP
0.700 GeneticVariation disease BEFREE Congenital leptin deficiency, a rare genetic disorder due to a homozygous mutation in the leptin gene (LEP), is accompanied by extreme obesity and hyperphagia. 23824601 2014
Entrez Id: 3952
Gene Symbol: LEP
LEP
0.700 GeneticVariation disease BEFREE We suggest that the LEP -2548 G/G homozygote plays a genetic recessive role in the development of extreme obesity in Taiwanese aborigines. 16571841 2006
Entrez Id: 3952
Gene Symbol: LEP
LEP
0.700 GeneticVariation disease BEFREE After adjusting for age, sex, fasting plasma glucose level, smoking, and exercise, obesity was associated with sum of dental diseases (ß = 0.239, p = .013), severe periodontitis (OR=4.52; 95% CI 1.37, 14.95, p = .013), adiponectin (ß = -0.359, p < .001), leptin (ß = 0.630, p < .001), and CRP levels (OR=12.66; 95% CI 3.07, 52.21, p < .001). 28513060 2017