impaired lipolysis Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description reduction in the rate of the hydrolysis of fat into free fatty acids (Mammalian Phenotype Ontology, MP_0008033)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0008033
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Genes

13 gene mutations causing the impaired lipolysis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ABHD5 abhydrolase domain containing 5
AZGP1 alpha-2-glycoprotein 1, zinc-binding
CAV1 caveolin 1, caveolae protein, 22kDa
CEBPB CCAAT/enhancer binding protein (C/EBP), beta
COL18A1 collagen, type XVIII, alpha 1
FABP4 fatty acid binding protein 4, adipocyte
FGF21 fibroblast growth factor 21
HCAR1 hydroxycarboxylic acid receptor 1
IRS1 insulin receptor substrate 1
MGLL monoglyceride lipase
PLIN1 perilipin 1
PNPLA2 patatin-like phospholipase domain containing 2
THRA thyroid hormone receptor, alpha