Leptin Deficiency Or Dysfunction Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link https://www.disgenet.org/browser/0/1/0/C3554224
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Genes

15 genes associated with the disease Leptin Deficiency Or Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
AGRP agouti related neuropeptide
CMKLR1 chemerin chemokine-like receptor 1
CNTF ciliary neurotrophic factor
FGF21 fibroblast growth factor 21
GPR1 G protein-coupled receptor 1
LEP leptin
LEPR leptin receptor
NPY2R neuropeptide Y receptor Y2
PPARG peroxisome proliferator-activated receptor gamma
RARRES2 retinoic acid receptor responder (tazarotene induced) 2
SERPINE1 serpin peptidase inhibitor, clade E (nexin, plasminogen activator inhibitor type 1), member 1
TBX1 T-box 1
TRH thyrotropin-releasing hormone
VEGFA vascular endothelial growth factor A
WNT5A wingless-type MMTV integration site family, member 5A