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Phenotypes Associated with This Genotype
Genotype
MGI:6358689
Allelic
Composition
Golga2tm1.1Baos/Golga2tm1.1Baos
Tg(Nes-cre)1Kln/0
Genetic
Background
involves: 129 * C57BL/6 * SJL
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Golga2tm1.1Baos mutation (0 available); any Golga2 mutation (53 available)
Tg(Nes-cre)1Kln mutation (4 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
N
• unlike germline null mice, mice are viable

nervous system
• elevated levels of apoptosis markers indicating increased Purkinje cell death
• decrease in the amount of plasma membrane AMPA-type glutamate receptor subunits in the postsynaptic density fraction from the cerebellum
• degeneration is first seen in lobules X and IX at 3 weeks of age and then spreads to other regions with age
• however, no degeneration of neurons is seen in the molecular or granule layers of the cerebellum
• decrease in dendrite size and arborization at P30
• dendrites at P30 are smaller than those at P9 indicating both failure to grow and atrophy
• loss of Purkinje cells beginning at 3 weeks of age
• becomes thinner with age in correlation with loss of Purkinje cells
• dramatically reduced in size

cellular
• compaction of the Golgi apparatus at P14 and P28 in Purkinje cells and a similar disruption is seen in granule cells in the cerebellum
• absence of Golgi outposts in primary dendrites of Purkinje cells at P8
• Golgi apparatus is located on the opposite side of the soma to the primary dendrite and the apparatus is dissociated from the centrosome indicating a loss of Golgi polarity in Purkinje cells at P14 and P28
• loss of cisternal stacking and cisternal length and an accumulation of vesicular profiles localized to the perinuclear region
• elevated levels of apoptosis markers indicating increased Purkinje cell death
• impaired secretory trafficking
• reduced soma to dendrite trafficking of GRIA2 in Purkinje cells

behavior/neurological
• limp reflex when lifted by the tail
• ataxic gait
• coordination defects are mild in young mice and progressively worsen with age
• slight reduction in time spent on a rotarod at 3 weeks of age and this reduction becomes more profound with age (8 and 12 weeks)
• require more time to cross balance beams of multiple sizes

growth/size/body
• growth retardation is less than that in germline null mice


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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last database update
12/17/2024
MGI 6.24
The Jackson Laboratory