Abstract
Obesity is a heritable and genetically influenced disorder. Recent studies have proved that obesity is a biochemically driven neurological disorder. Obesity has a complex and heterogeneous genetic and phenotypic manifestation. Familial obesity is monogenic and common obesity is polygenic. Leptin and its receptor (LEPR), the α-melanocortin-stimulating hormone receptor (MC4R), pro-opiomelanocortin (POMC) and prohormone subtilisin/kexin type 1 (PCSK1) are some of the single genes involved in monogenic obesity. Glutamate Decarboxylase 2 gene (GAD2) gene is thought to be part of a polygene system resulting in common obesity. GAD2 coding sequence is present on chromosome 10p locus and encodes for a protein GAD65. This protein catalyzes ...
