amylo-alpha-1, 6-glucosidase, 4-alpha-glucanotransferase

Summary
Gene Symbol
  • AGL
Aliases
  • GDE
  • glycogen debranching enzyme
  • glycogen storage disease type III
Organism
Homo sapiens (human)
External Links
NCBI Gene
178
HGNC
321
KEGG Gene ID
hsa:178
PubChem
178
Alliance of Genome Resources
Annotation
Keyword
  • Alternative splicing
  • Cytoplasm
  • Direct protein sequencing
  • Disease variant
  • Glycogen biosynthesis
  • Glycogen storage disease
  • Glycosidase
  • Glycosyltransferase
  • Multifunctional enzyme
  • Phosphoprotein
  • Reference proteome
  • Ubl conjugation
Proteins
Displaying all 2 entries
UniProt Protein Name
A0A0S2A4E4
  • Glycogen debrancher
P35573
  • Glycogen debrancher
Gene Ontology (GO)
GO Hierarchy
KEGG BRITE Database
Orthology
K01196
Name
glycogen debranching enzyme [EC:2.4.1.25 3.2.1.33]
References
Disease
Disease Ontology
Displaying entries 41 - 50 of 91 in total
DO ID Disease Name Source
DOID:0110306 autosomal dominant limb-girdle muscular dystrophy type 3
DOID:0111040 glycogen storage disease IXd
DOID:0111041 glycogen storage disease IXb
DOID:0111042 glycogen storage disease IXa
DOID:0111043 glycogen storage disease IXc
DOID:0111135 congenital generalized lipodystrophy type 1
DOID:0111136 congenital generalized lipodystrophy type 2
DOID:0111137 congenital generalized lipodystrophy type 3
DOID:0111138 congenital generalized lipodystrophy type 4
DOID:0111338 isolated elevated serum creatine phosphokinase levels
The Human Phenotype Ontology
Displaying entries 21 - 24 of 24 in total
HPO ID HPO Term
HP:0003693 Distal amyotrophy
HP:0004322 Short stature
HP:0005280 Depressed nasal bridge
HP:0011800 Midface retrusion
Displaying all 2 entries
Disease ID Disease Name
OMIM:232400
  • glycogen storage disease III
ORPHA:366
  • glycogen storage disease III

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: August 19, 2024