MGP Database

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MGP000098

Ontology/Pathway Information

Entrez Gene ID178
Gene Nameamylo-alpha-1, 6-glucosidase, 4-alpha-glucanotransferase
Gene Symbol AGL
SpeciesHomo sapiens
Gene Ontology (GO Annotations)
GO IDSourceTypeDescription
GO:0005737 IDA:UniProtKBCcytoplasm
GO:0005829 TAS:ReactomeCcytosol
GO:0016234 IEA:EnsemblCinclusion body
GO:0043033 TAS:ProtIncCisoamylase complex
GO:0005634 IDA:HPACnucleus
GO:0016529 IEA:EnsemblCsarcoplasmic reticulum
GO:0004134 IBA:RefGenomeF4-alpha-glucanotransferase activity
GO:0004135 IBA:RefGenomeFamylo-alpha-1,6-glucosidase activity
GO:0004133 TAS:ProtIncFglycogen debranching enzyme activity
GO:0030247 IEA:EnsemblFpolysaccharide binding
GO:0005975 TAS:ReactomePcarbohydrate metabolic process
GO:0006006 TAS:ReactomePglucose metabolic process
GO:0005978 IEA:UniProtKB-KWPglycogen biosynthetic process
GO:0005980 IBA:RefGenomePglycogen catabolic process
GO:0051384 IEA:EnsemblPresponse to glucocorticoid
GO:0007584 IEA:EnsemblPresponse to nutrient
GO:0044281 TAS:ReactomePsmall molecule metabolic process
REACTOME Pathway Links
REACTOME Pathway IDDescription
REACT_116125Disease
REACT_723Glucose metabolism
REACT_1008Glycogen breakdown (glycogenolysis)
REACT_264090Glycogen storage diseases
REACT_111217Metabolism
REACT_474Metabolism of carbohydrates
REACT_264430Myoclonic epilepsy of Lafora
SMP Pathway Links
SMP IDDescription
SMP00553Glycogenosis, Type III. Cori disease, Debrancher glycogenosis
SMP00554Glycogenosis, Type IV. Amylopectinosis, Anderson disease
SMP00555Glycogenosis, Type VI. Hers disease
SMP00552Glycogen synthetase deficiency
SMP00556Mucopolysaccharidosis VI. Sly syndrome
SMP00058Starch and Sucrose Metabolism
SMP00557Sucrase-isomaltase deficiency
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