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Symbol
Name
ID

Gbe1
1,4-alpha-glucan branching enzyme 1
MGI:1921435

Phenotype annotations related to muscle

Darker colors indicate more annotations

Human Phenotypes	Flexion contracture	Arthrogryposis multiplex congenita	Hypotonia	Muscle weakness	Skeletal muscle atrophy
Disease(s) Associated with GBE1
glycogen storage disease IV

Mouse Phenotypes		decreased cardiac muscle glycogen level	thin myocardium	abnormal fetal cardiomyocyte proliferation	abnormal muscle glycogen level	decreased skeletal muscle glycogen level	increased skeletal muscle glycogen level	abnormal skeletal muscle morphology	abnormal muscle physiology
Availability	Mouse Genotype	decreased cardiac muscle glycogen level	thin myocardium	abnormal fetal cardiomyocyte proliferation	abnormal muscle glycogen level	decreased skeletal muscle glycogen level	increased skeletal muscle glycogen level	abnormal skeletal muscle morphology	abnormal muscle physiology
	Gbe1^m1Yty/Gbe1^m1Yty
	Gbe1^tm1.1Hoa/Gbe1^tm1.1Hoa
	Gbe1^tm1Hoa/Gbe1^tm1Hoa
	Gbe1^tm2.1Hoa/Gbe1^tm2.1Hoa
	Gbe1^tm2Hoa/Gbe1^tm2Hoa

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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