Gene: LEP ×
Source: CURATED ×
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 3952
Gene Symbol: LEP
LEP 		0.800 GeneticVariation disease UNIPROT Biologically inactive leptin and early-onset extreme obesity. 25551525 2015
Entrez Id: 3952
Gene Symbol: LEP
LEP 		0.800 GermlineCausalMutation disease ORPHANET Monogenic forms of childhood obesity due to mutations in the leptin gene. 26567097 2014
Entrez Id: 3952
Gene Symbol: LEP
LEP 		0.800 GeneticVariation disease UNIPROT A leptin missense mutation associated with hypogonadism and morbid obesity. 9500540 1998
Entrez Id: 3952
Gene Symbol: LEP
LEP 		0.800 Biomarker disease GENOMICS_ENGLAND
Entrez Id: 3952
Gene Symbol: LEP
LEP 		0.800 Biomarker disease CTD_human