MGP Database

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MGP002179

Ontology/Pathway Information

Entrez Gene ID5019
Gene Name3-oxoacid CoA transferase 1
Gene Symbol OXCT1
SpeciesHomo sapiens
Gene Ontology (GO Annotations)
GO IDSourceTypeDescription
GO:0005759 TAS:ReactomeCmitochondrial matrix
GO:0005739 IDA:UniProtKBCmitochondrion
GO:0008260 IMP:UniProtKBF3-oxoacid CoA-transferase activity
GO:0042803 NAS:UniProtKBFprotein homodimerization activity
GO:0060612 IEA:EnsemblPadipose tissue development
GO:0007420 IEA:EnsemblPbrain development
GO:0046950 IMP:UniProtKBPcellular ketone body metabolic process
GO:0044255 TAS:ReactomePcellular lipid metabolic process
GO:0007507 IEA:EnsemblPheart development
GO:0046952 TAS:ReactomePketone body catabolic process
GO:0042182 IEA:EnsemblPketone catabolic process
GO:0035774 IEA:EnsemblPpositive regulation of insulin secretion involved in cellular response to glucose stimulus
GO:0014823 IEA:EnsemblPresponse to activity
GO:0042493 IEA:EnsemblPresponse to drug
GO:0045471 IEA:EnsemblPresponse to ethanol
GO:0009725 IEA:EnsemblPresponse to hormone
GO:0007584 IEA:EnsemblPresponse to nutrient
GO:0042594 IEA:EnsemblPresponse to starvation
GO:0044281 TAS:ReactomePsmall molecule metabolic process
REACTOME Pathway Links
REACTOME Pathway IDDescription
REACT_22279Fatty acid, triacylglycerol, and ketone body metabolism
REACT_1861Ketone body metabolism
REACT_111217Metabolism
REACT_22258Metabolism of lipids and lipoproteins
REACT_59Utilization of Ketone Bodies
SMP Pathway Links
SMP IDDescription
SMP001372-Methyl-3-Hydroxybutryl CoA Dehydrogenase Deficiency
SMP001383-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency
SMP005213-hydroxyisobutyric acid dehydrogenase deficiency
SMP005223-hydroxyisobutyric aciduria
SMP002373-Methylcrotonyl Coa Carboxylase Deficiency Type I
SMP001393-Methylglutaconic Aciduria Type I
SMP001403-Methylglutaconic Aciduria Type III
SMP001413-Methylglutaconic Aciduria Type IV
SMP00173Beta-Ketothiolase Deficiency
SMP00073Butyrate Metabolism
SMP00523Isobutyryl-coa dehydrogenase deficiency
SMP00524Isovaleric acidemia
SMP00238Isovaleric Aciduria
SMP00071Ketone Body Metabolism
SMP00199Maple Syrup Urine Disease
SMP00384Methylmalonate Semialdehyde Dehydrogenase Deficiency
SMP00200Methylmalonic Aciduria
SMP00236Propionic Acidemia
SMP00569Succinyl CoA: 3-ketoacid CoA transferase deficiency
SMP00032Valine, Leucine and Isoleucine Degradation
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