MGP Database

MGP006161

Ontology/Pathway Information

Entrez Gene ID	84693
Gene Name	methylmalonyl CoA epimerase
Gene Symbol	MCEE
Species	Homo sapiens

Gene Ontology (GO Annotations)

GO ID	Source	Type	Description
GO:0005759	TAS:Reactome	C	mitochondrial matrix
GO:0046872	IEA:UniProtKB-KW	F	metal ion binding
GO:0004493	IDA:UniProtKB	F	methylmalonyl-CoA epimerase activity
GO:0044255	TAS:Reactome	P	cellular lipid metabolic process
GO:0006635	TAS:Reactome	P	fatty acid beta-oxidation
GO:0046491	IDA:UniProtKB	P	L-methylmalonyl-CoA metabolic process
GO:0019626	TAS:Reactome	P	short-chain fatty acid catabolic process
GO:0044281	TAS:Reactome	P	small molecule metabolic process

REACTOME Pathway Links

REACTOME Pathway ID	Description
REACT_22279	Fatty acid, triacylglycerol, and ketone body metabolism
REACT_111217	Metabolism
REACT_22258	Metabolism of lipids and lipoproteins
REACT_1473	Mitochondrial Fatty Acid Beta-Oxidation
REACT_993	Propionyl-CoA catabolism

SMP Pathway Links

SMP ID	Description
SMP00137	2-Methyl-3-Hydroxybutryl CoA Dehydrogenase Deficiency
SMP00138	3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency
SMP00521	3-hydroxyisobutyric acid dehydrogenase deficiency
SMP00522	3-hydroxyisobutyric aciduria
SMP00237	3-Methylcrotonyl Coa Carboxylase Deficiency Type I
SMP00139	3-Methylglutaconic Aciduria Type I
SMP00140	3-Methylglutaconic Aciduria Type III
SMP00141	3-Methylglutaconic Aciduria Type IV
SMP00173	Beta-Ketothiolase Deficiency
SMP00523	Isobutyryl-coa dehydrogenase deficiency
SMP00524	Isovaleric acidemia
SMP00238	Isovaleric Aciduria
SMP00198	Malonic Aciduria
SMP00502	Malonyl-coa decarboxylase deficiency
SMP00199	Maple Syrup Urine Disease
SMP00384	Methylmalonate Semialdehyde Dehydrogenase Deficiency
SMP00200	Methylmalonic Aciduria
SMP00201	Methylmalonic Aciduria Due to Cobalamin-Related Disorders
SMP00016	Propanoate Metabolism
SMP00236	Propionic Acidemia
SMP00452	Threonine and 2-Oxobutanoate Degradation
SMP00032	Valine, Leucine and Isoleucine Degradation