decreased circulating glycerol level Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description reduced blood level of trihydroxy sugar alcohols that are precursors for synthesis of triacylglycerols, and of phospholipids and cellular glucose in the liver and adipose tissue; fat catabolism results in the release of glycerol and fatty acids into the bloodstream to be used as an energy source (Mammalian Phenotype Ontology, MP_0003442)
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18 gene mutations causing the decreased circulating glycerol level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
AQP7 aquaporin 7
ATP8B2 ATPase, aminophospholipid transporter, class I, type 8B, member 2
BSCL2 Berardinelli-Seip congenital lipodystrophy 2 (seipin)
CDH23 cadherin-related 23
CES1 carboxylesterase 1
DOPEY2 dopey family member 2
EPB41L5 erythrocyte membrane protein band 4.1 like 5
LIPE lipase, hormone-sensitive
MGLL monoglyceride lipase
MYSM1 Myb-like, SWIRM and MPN domains 1
NR1D2 nuclear receptor subfamily 1, group D, member 2
NSUN2 NOP2/Sun RNA methyltransferase family, member 2
P2RY13 purinergic receptor P2Y, G-protein coupled, 13
PARVB parvin, beta
SETMAR SET domain and mariner transposase fusion gene
SLC25A4 solute carrier family 25 (mitochondrial carrier; adenine nucleotide translocator), member 4
THRB thyroid hormone receptor, beta
TMEM189 transmembrane protein 189