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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Gaatm2Rabn
targeted mutation 2, Nina Raben
MGI:2179960
Summary 1 genotype
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Gaatm2Rabn/Gaatm2Rabn involves: 129X1/SvJ * C57BL/6 MGI:3624423


Genotype
MGI:3624423
hm1
Allelic
Composition
Gaatm2Rabn/Gaatm2Rabn
Genetic
Background
involves: 129X1/SvJ * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Gaatm2Rabn mutation (0 available); any Gaa mutation (54 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
behavior/neurological
• severely impaired on a rotarod at 8-11 months of age
• observe waddling gait by 7-9 moths of age
• exhibit signs of reduced activity in an open field environment at 4-6 months of age
• by 16-18 months of age, exhibit near paralysis of the hind limbs leading to abnormal posture of hind limbs

muscle
• massive accumulation of glycogen in heart
• massive accumulation of glycogen in skeletal muscle and diaphragm
• observe muscle weakness by 7-9 months of age that progresses with age
• develop a progressive muscle wasting disorder with clinical features of glycogen storage disease II; average age of onset is 6.6 months for females and 8.3 months for males

cardiovascular system
• massive accumulation of glycogen in heart

homeostasis/metabolism
• massive accumulation of glycogen in heart
• massive accumulation of glycogen in brain
• massive accumulation of glycogen in skeletal muscle and diaphragm

skeleton
• progressive development of profound kyphosis

nervous system
• massive accumulation of glycogen in brain

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
glycogen storage disease II DOID:2752 OMIM:232300
J:76435





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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
04/30/2024
MGI 6.23
The Jackson Laboratory