enhanced lipolysis Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description increase in the rate of the hydrolysis of fat into free fatty acids (Mammalian Phenotype Ontology, MP_0008034)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0008034
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Genes

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

Symbol Name
ANGPTL4 angiopoietin-like 4
BSCL2 Berardinelli-Seip congenital lipodystrophy 2 (seipin)
CAV1 caveolin 1, caveolae protein, 22kDa
CCDC80 coiled-coil domain containing 80
CERS6 ceramide synthase 6
CIDEA cell death-inducing DFFA-like effector a
CIDEC cell death-inducing DFFA-like effector c
CTF1 cardiotrophin 1
FGF21 fibroblast growth factor 21
G0S2 G0/G1 switch 2
LGALS12 lectin, galactoside-binding, soluble, 12
MPG N-methylpurine-DNA glycosylase
PDE3B phosphodiesterase 3B, cGMP-inhibited
PLIN1 perilipin 1
RASGRF1 Ras protein-specific guanine nucleotide-releasing factor 1
SERTAD2 SERTA domain containing 2