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Symbol
Name
ID
Agl
amylo-1,6-glucosidase, 4-alpha-glucanotransferase
MGI:1924809
Phenotype annotations related to homeostasis/metabolism
Darker colors indicate more annotations
Human Phenotypes
Hyperlipidemia
Elevated serum creatine kinase
Hypoglycemia
Disease(s) Associated with AGL
glycogen storage disease III

Mouse Phenotypes
impaired exercise endurance
increased cardiac muscle glycogen level
decreased fasting circulating glucose level
decreased circulating glucose level
hypoglycemia
increased circulating alanine transaminase level
increased circulating alkaline phosphatase level
increased circulating aspartate transaminase level
increased circulating creatine kinase level
increased brain glycogen level
increased liver glycogen level
increased skeletal muscle glycogen level
increased glycogen level
Availability Mouse Genotype
Agltm1a(EUCOMM)Wtsi/Agltm1a(EUCOMM)Wtsi
Agltm1Geno/Agltm1Geno

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB), Gene Ontology (GO)
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last database update
03/24/2020
MGI 6.15
The Jackson Laboratory