MGP Database

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MGP001949

Ontology/Pathway Information

Entrez Gene ID4329
Gene Namealdehyde dehydrogenase 6 family, member A1
Gene Symbol ALDH6A1
SpeciesHomo sapiens
Gene Ontology (GO Annotations)
GO IDSourceTypeDescription
GO:0070062 IDA:UniProtKBCextracellular vesicular exosome
GO:0005759 TAS:ReactomeCmitochondrial matrix
GO:0005739 NAS:UniProtKBCmitochondrion
GO:0005654 IDA:HPACnucleoplasm
GO:0004029 IBA:GO_CentralFaldehyde dehydrogenase (NAD) activity
GO:0000062 ISS:UniProtKBFfatty-acyl-CoA binding
GO:0018478 ISS:UniProtKBFmalonate-semialdehyde dehydrogenase (acetylating) activity
GO:0004491 ISS:UniProtKBFmethylmalonate-semialdehyde dehydrogenase (acylating) activity
GO:0044822 IDA:UniProtKBFpoly(A) RNA binding
GO:0009083 TAS:ReactomePbranched-chain amino acid catabolic process
GO:0050873 IEA:EnsemblPbrown fat cell differentiation
GO:0034641 TAS:ReactomePcellular nitrogen compound metabolic process
GO:0044281 TAS:ReactomePsmall molecule metabolic process
GO:0006210 IMP:BHF-UCLPthymine catabolic process
GO:0019859 ISS:UniProtKBPthymine metabolic process
GO:0006574 IMP:BHF-UCLPvaline catabolic process
GO:0006573 ISS:UniProtKBPvaline 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
SMP00007Beta-Alanine Metabolism
SMP00173Beta-Ketothiolase Deficiency
SMP00493Carnosinuria, carnosinemia
SMP00351GABA-Transaminase Deficiency
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
SMP00492Ureidopropionase deficiency
SMP00032Valine, Leucine and Isoleucine Degradation
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