MGP Database

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MGP000006

Ontology/Pathway Information

Entrez Gene ID18
Gene Name4-aminobutyrate aminotransferase
Gene Symbol ABAT
SpeciesHomo sapiens
Gene Ontology (GO Annotations)
GO IDSourceTypeDescription
GO:0032144 IDA:UniProtKBC4-aminobutyrate transaminase complex
GO:0070062 IDA:UniProtKBCextracellular vesicular exosome
GO:0005759 TAS:ReactomeCmitochondrial matrix
GO:0005739 ISS:UniProtKBCmitochondrion
GO:0043005 IEA:EnsemblCneuron projection
GO:0003867 TAS:ReactomeF4-aminobutyrate transaminase activity
GO:0042803 IPI:UniProtKBFprotein homodimerization activity
GO:0030170 IDA:UniProtKBFpyridoxal phosphate binding
GO:0047298 IEA:UniProtKB-ECF(S)-3-amino-2-methylpropionate transaminase activity
GO:0032145 ISS:UniProtKBFsuccinate-semialdehyde dehydrogenase binding
GO:0048148 ISS:UniProtKBPbehavioral response to cocaine
GO:0007620 IEA:EnsemblPcopulation
GO:0009450 NAS:UniProtKBPgamma-aminobutyric acid catabolic process
GO:0007626 IEA:EnsemblPlocomotory behavior
GO:0045776 IEA:EnsemblPnegative regulation of blood pressure
GO:0042135 NAS:UniProtKBPneurotransmitter catabolic process
GO:0007269 TAS:ReactomePneurotransmitter secretion
GO:0042493 IEA:EnsemblPresponse to drug
GO:0045471 IEA:EnsemblPresponse to ethanol
GO:0001666 IEA:EnsemblPresponse to hypoxia
GO:0010039 IEA:EnsemblPresponse to iron ion
GO:0035094 IEA:EnsemblPresponse to nicotine
GO:0007268 TAS:ReactomePsynaptic transmission
REACTOME Pathway Links
REACTOME Pathway IDDescription
REACT_23964Degradation of GABA
REACT_23947GABA synthesis, release, reuptake and degradation
REACT_13685Neuronal System
REACT_13723Neurotransmitter Release Cycle
REACT_13477Transmission across Chemical Synapses
SMP Pathway Links
SMP IDDescription
SMP001362-Hydroxyglutric Aciduria (D And L Form)
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
SMP002434-Hydroxybutyric Aciduria/Succinic Semialdehyde Dehydrogenase Deficiency
SMP00067Aspartate Metabolism
SMP00007Beta-Alanine Metabolism
SMP00173Beta-Ketothiolase Deficiency
SMP00175Canavan Disease
SMP00493Carnosinuria, carnosinemia
SMP00351GABA-Transaminase Deficiency
SMP00072Glutamate Metabolism
SMP00385Homocarnosinosis
SMP00339Hyperinsulinism-Hyperammonemia Syndrome
SMP00192Hypoacetylaspartia
SMP00523Isobutyryl-coa dehydrogenase deficiency
SMP00524Isovaleric acidemia
SMP00238Isovaleric Aciduria
SMP00198Malonic Aciduria
SMP00502Malonyl-coa decarboxylase deficiency
SMP00199Maple Syrup Urine Disease
SMP00384Methylmalonate Semialdehyde Dehydrogenase Deficiency
SMP00200Methylmalonic Aciduria
SMP00201Methylmalonic Aciduria Due to Cobalamin-Related Disorders
SMP00016Propanoate Metabolism
SMP00236Propionic Acidemia
SMP00567Succinic semialdehyde dehydrogenase deficiency
SMP00492Ureidopropionase deficiency
SMP00032Valine, Leucine and Isoleucine Degradation
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