MGP Database

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MGP001173

Ontology/Pathway Information

Entrez Gene ID2639
Gene Nameglutaryl-CoA dehydrogenase
Gene Symbol GCDH
SpeciesHomo sapiens
Gene Ontology (GO Annotations)
GO IDSourceTypeDescription
GO:0005743 IEA:EnsemblCmitochondrial inner membrane
GO:0005759 TAS:ReactomeCmitochondrial matrix
GO:0005739 IDA:HPACmitochondrion
GO:0000062 IEA:EnsemblFfatty-acyl-CoA binding
GO:0050660 IEA:InterProFflavin adenine dinucleotide binding
GO:0004361 EXP:ReactomeFglutaryl-CoA dehydrogenase activity
GO:0034641 TAS:ReactomePcellular nitrogen compound metabolic process
GO:0019395 IEA:EnsemblPfatty acid oxidation
GO:0046949 IEA:EnsemblPfatty-acyl-CoA biosynthetic process
GO:0006554 TAS:ReactomePlysine catabolic process
GO:0044281 TAS:ReactomePsmall molecule metabolic process
GO:0006568 IEA:UniProtKB-UniPathwayPtryptophan metabolic process
REACTOME Pathway Links
REACTOME Pathway IDDescription
REACT_1298Lysine catabolism
REACT_111217Metabolism
REACT_13Metabolism of amino acids and derivatives
SMP Pathway Links
SMP IDDescription
SMP007192-aminoadipic 2-oxoadipic aciduria
SMP00538Carnitine palmitoyl transferase deficiency (I)
SMP00541Carnitine palmitoyl transferase deficiency (II)
SMP00181Ethylmalonic Encephalopathy
SMP00051Fatty acid Metabolism
SMP00185Glutaric Aciduria Type I
SMP00186Glutaric Aciduria Type III
SMP00527Hyperlysinemia I, Familial
SMP00528Hyperlysinemia II or Saccharopinuria
SMP00539Long chain acyl-CoA dehydrogenase deficiency (LCAD)
SMP00037Lysine Degradation
SMP00542Medium chain acyl-coa dehydrogenase deficiency (MCAD)
SMP00571Pyridoxine dependency with seizures
SMP00239Saccharopinuria/Hyperlysinemia II
SMP00235Short Chain Acyl CoA Dehydrogenase Deficiency (SCAD Deficiency)
SMP00545Trifunctional protein deficiency
SMP00540Very-long-chain acyl coa dehydrogenase deficiency (VLCAD)
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