decreased circulating ketone body level Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description less than the normal amount of acetoacetate, 3-hydroxybutyrate (beta-hydroxybutyrate) and/or acteone in the blood, which are produced by fatty acid and carbohydrate metabolism and seen in conditions such as starvation and diabetes mellitus (Mammalian Phenotype Ontology, MP_0003458)
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11 gene mutations causing the decreased circulating ketone body level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ACOT13 acyl-CoA thioesterase 13
AGRP agouti related neuropeptide
BCAT2 branched chain amino-acid transaminase 2, mitochondrial
CIDEC cell death-inducing DFFA-like effector c
FGF21 fibroblast growth factor 21
HADH hydroxyacyl-CoA dehydrogenase
MGLL monoglyceride lipase
PCK1 phosphoenolpyruvate carboxykinase 1 (soluble)
SLC27A5 solute carrier family 27 (fatty acid transporter), member 5
SLC2A4 solute carrier family 2 (facilitated glucose transporter), member 4
TSC1 tuberous sclerosis 1