Symbol Name ID |
Gbe1
1,4-alpha-glucan branching enzyme 1 MGI:1921435 |
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 |
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Availability | Mouse Genotype | ||||||||
Gbe1m1Yty/Gbe1m1Yty | |||||||||
Gbe1tm1.1Hoa/Gbe1tm1.1Hoa | |||||||||
Gbe1tm1Hoa/Gbe1tm1Hoa | |||||||||
Gbe1tm2.1Hoa/Gbe1tm2.1Hoa | |||||||||
Gbe1tm2Hoa/Gbe1tm2Hoa |
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 08/02/2024 MGI 6.24 |
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