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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Gbe1tm2.1Hoa
targeted mutation 2.1, H Orhan Akman
MGI:5767122
Summary 1 genotype
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Gbe1tm2.1Hoa/Gbe1tm2.1Hoa involves: 129S7/SvEvBrd MGI:5767124


Genotype
MGI:5767124
hm1
Allelic
Composition
Gbe1tm2.1Hoa/Gbe1tm2.1Hoa
Genetic
Background
involves: 129S7/SvEvBrd
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Gbe1tm2.1Hoa mutation (0 available); any Gbe1 mutation (47 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• mice survive up to 80 weeks

behavior/neurological
• mice exhibit significant weakness
• mice show spastic paraplegia and cannot use their hind limbs after 1 year of age

homeostasis/metabolism
• increase in serum creatine kinase activity
• accumulation of poorly branched from of glycogen, polyglucosan, in the neuropil, skeletal muscle, cardiac muscle, and liver
• newborns show accumulation of polyglucosan bodies in choroid plexus, brain stem, muscle, dorsal root ganglion cells, liver, and epithelial cells of the brain, but not in the cerebral cortex or heart muscle
• accumulated polyglucosan bodies are ubiquitinylated
• muscle glycogen content is increased
• brain, heart, liver, and muscle glycogen content is increased

liver/biliary system
• brain, heart, liver, and muscle glycogen content is increased
• moderate perisinusoidal/pericellular dense collagen bundles are seen in the liver, indicating fibrosis

muscle
• muscle glycogen content is increased

nervous system

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
glycogen storage disease IV DOID:2750 OMIM:232500
J:226481





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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
11/12/2024
MGI 6.24
The Jackson Laboratory