MGP Database

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MGP000021

Ontology/Pathway Information

Entrez Gene ID36
Gene Nameacyl-CoA dehydrogenase, short/branched chain
Gene Symbol ACADSB
SpeciesHomo sapiens
Gene Ontology (GO Annotations)
GO IDSourceTypeDescription
GO:0070062 IDA:UniProtKBCextracellular vesicular exosome
GO:0005759 TAS:ReactomeCmitochondrial matrix
GO:0005739 IDA:HPACmitochondrion
GO:0003995 EXP:ReactomeFacyl-CoA dehydrogenase activity
GO:0050660 IEA:InterProFflavin adenine dinucleotide binding
GO:0009083 TAS:ReactomePbranched-chain amino acid catabolic process
GO:0034641 TAS:ReactomePcellular nitrogen compound metabolic process
GO:0006631 TAS:ProtIncPfatty acid metabolic process
GO:0044281 TAS:ReactomePsmall molecule metabolic process
REACTOME Pathway Links
REACTOME Pathway IDDescription
REACT_197Branched-chain amino acid catabolism
REACT_111217Metabolism
REACT_13Metabolism of amino acids and derivatives
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
SMP00538Carnitine palmitoyl transferase deficiency (I)
SMP00541Carnitine palmitoyl transferase deficiency (II)
SMP00181Ethylmalonic Encephalopathy
SMP00051Fatty acid Metabolism
SMP00185Glutaric Aciduria Type I
SMP00523Isobutyryl-coa dehydrogenase deficiency
SMP00524Isovaleric acidemia
SMP00238Isovaleric Aciduria
SMP00539Long chain acyl-CoA dehydrogenase deficiency (LCAD)
SMP00199Maple Syrup Urine Disease
SMP00542Medium chain acyl-coa dehydrogenase deficiency (MCAD)
SMP00384Methylmalonate Semialdehyde Dehydrogenase Deficiency
SMP00200Methylmalonic Aciduria
SMP00236Propionic Acidemia
SMP00235Short Chain Acyl CoA Dehydrogenase Deficiency (SCAD Deficiency)
SMP00545Trifunctional protein deficiency
SMP00032Valine, Leucine and Isoleucine Degradation
SMP00635Valproic Acid Metabolism Pathway
SMP00540Very-long-chain acyl coa dehydrogenase deficiency (VLCAD)
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