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Symbol
Name
ID

Agl
amylo-1,6-glucosidase, 4-alpha-glucanotransferase
MGI:1924809

Phenotype annotations related to muscle

Darker colors indicate more annotations

Human Phenotypes	Muscle weakness	Distal amyotrophy	Myopathy
Disease(s) Associated with AGL
glycogen storage disease III

Mouse Phenotypes		increased cardiac muscle glycogen level	increased skeletal muscle glycogen level	muscle weakness
Availability	Mouse Genotype	increased cardiac muscle glycogen level	increased skeletal muscle glycogen level	muscle weakness
	Agl^{tm1a(EUCOMM)Wtsi}/Agl^{tm1a(EUCOMM)Wtsi}
	Agl^tm1Geno/Agl^tm1Geno

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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