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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Tg(CAG-EPM2A*C266S)1Bmin
transgene insertion 1, Berge A Minassian
MGI:6459753
Summary 1 genotype
Jump to Allelic Composition Genetic Background Genotype ID
tg1
Tg(CAG-EPM2A*C266S)1Bmin/0 involves: 129 * C57BL/6 * SJL MGI:6459755


Genotype
MGI:6459755
tg1
Allelic
Composition
Tg(CAG-EPM2A*C266S)1Bmin/0
Genetic
Background
involves: 129 * C57BL/6 * SJL
Find Mice Using the International Mouse Strain Resource (IMSR)
No mouse lines available in IMSR.
See publication links below for author information.
phenotype observed in females
phenotype observed in males
N normal phenotype
homeostasis/metabolism
• muscle contains approximately 2x as much glycogen as wild-type mice
• glycogen synthase activity in the presence of glucose-6-P is increased by about 50% in muscle

nervous system
N
• mice do not exhibit seizures or neurodegeneration
• all mice exhibit Lafora body formation; Lafora body formation is extensive in the hippocampus, with smaller amounts in the basal forebrain and sparse amounts in the rest of the brain
• 12 month old mice have more Lafora bodies than younger mice but no further increase in seen at 20 months
• Lafora bodies are in the neuropil and within neuronal cell bodies but not in axonal tracts or glia and are mostly spherical in shape with dense accumulation of fibrillar material in the center
• Lafora bodies are near the perinuclear ER in the soma and within dendrites in the neuropil
• a high proportion of skeletal muscle fibers contain large polyglucosan pools, present primarily in the subsarcolemma adjacent to myonuclei and at the neuromuscular junctions and some in the sarcoplasm between sarcomeres
• the myocardium shows accumulation of large polyglucosan pools
• numerous Lafora bodies are seen in hepatocytes, occupying the majority of the cytoplasm and displacing the nucleus and other organelles peripherally; Lafora bodies consist of a mixture of polyglucosan fibrils and glycogen rosettes

muscle
• muscle contains approximately 2x as much glycogen as wild-type mice

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
Lafora disease DOID:3534 OMIM:254780
J:120356 , J:262504





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last database update
12/10/2024
MGI 6.24
The Jackson Laboratory