Congenital Generalized Lipodystrophy Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description OMIM mapping confirmed by DO. [SN]. (Human Disease Ontology, DOID_0050585)
External Link https://www.disgenet.org/browser/0/1/0/C1720862
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Genes

11 genes associated with the disease Congenital Generalized Lipodystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ADIPOQ adiponectin, C1Q and collagen domain containing
ADRB3 adrenoceptor beta 3
AGPAT2 1-acylglycerol-3-phosphate O-acyltransferase 2
AGPS alkylglycerone phosphate synthase
BSCL2 Berardinelli-Seip congenital lipodystrophy 2 (seipin)
GHRL ghrelin/obestatin prepropeptide
GZMB granzyme B (granzyme 2, cytotoxic T-lymphocyte-associated serine esterase 1)
LEP leptin
NUCB2 nucleobindin 2
PNPLA2 patatin-like phospholipase domain containing 2
PPARG peroxisome proliferator-activated receptor gamma