MGP Database

MGP000118

Ontology/Pathway Information

Entrez Gene ID218
Gene Namealdehyde dehydrogenase 3 family, member A1
Gene Symbol ALDH3A1
SpeciesHomo sapiens
Gene Ontology (GO Annotations)
GO IDSourceTypeDescription
GO:0005737 IDA:HPACcytoplasm
GO:0005829 ISS:UniProtKBCcytosol
GO:0005783 IDA:LIFEdbCendoplasmic reticulum
GO:0005615 IDA:UniProtKBCextracellular space
GO:0005886 IDA:HPACplasma membrane
GO:0004028 IEA:EnsemblF3-chloroallyl aldehyde dehydrogenase activity
GO:0008106 IDA:UniProtKBFalcohol dehydrogenase (NADP+) activity
GO:0004029 IDA:UniProtKBFaldehyde dehydrogenase (NAD) activity
GO:0004030 IEA:UniProtKB-ECFaldehyde dehydrogenase [NAD(P)+] activity
GO:0007568 IEA:EnsemblPaging
GO:0006081 IDA:UniProtKBPcellular aldehyde metabolic process
GO:0055114 IDA:UniProtKBPoxidation-reduction process
GO:0008284 IEA:EnsemblPpositive regulation of cell proliferation
GO:0051591 IEA:EnsemblPresponse to cAMP
GO:0042493 IEA:EnsemblPresponse to drug
GO:0051384 IEA:EnsemblPresponse to glucocorticoid
GO:0001666 IEA:EnsemblPresponse to hypoxia
GO:0007584 IEA:EnsemblPresponse to nutrient
SMP Pathway Links
SMP IDDescription
SMP00169Alkaptonuria
SMP00447Cyclophosphamide Action Pathway
SMP00604Cyclophosphamide Metabolism Pathway
SMP00529D-glyceric acidura
SMP00429Disulfiram Action Pathway
SMP00498Dopamine beta-hydroxylase deficiency
SMP00530Familial lipoprotein lipase deficiency
SMP00633Felbamate Metabolism Pathway
SMP00039Glycerolipid Metabolism
SMP00187Glycerol Kinase Deficiency
SMP00190Hawkinsinuria
SMP00044Histidine Metabolism
SMP00191Histidinemia
SMP00448Ifosfamide Action Pathway
SMP00605Ifosfamide Metabolism Pathway
SMP00533Monoamine oxidase-a deficiency (MAO-A)
SMP00006Tyrosine Metabolism
SMP00494Tyrosinemia, transient, of the newborn
SMP00218Tyrosinemia Type I
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