weight loss Gene Set

Dataset GAD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description Reduction inexisting body weight. (Human Phenotype Ontology, HP_0001824)
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Genes

10 genes associated with the disease weight loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Symbol Name
ABCG5 ATP-binding cassette, sub-family G (WHITE), member 5
ABCG8 ATP-binding cassette, sub-family G (WHITE), member 8
AR androgen receptor
GRIN1 glutamate receptor, ionotropic, N-methyl D-aspartate 1
HTR2C 5-hydroxytryptamine (serotonin) receptor 2C, G protein-coupled
PLA2G2D phospholipase A2, group IID
PLIN1 perilipin 1
PPARG peroxisome proliferator-activated receptor gamma
SLC6A2 solute carrier family 6 (neurotransmitter transporter), member 2
UCP2 uncoupling protein 2 (mitochondrial, proton carrier)