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Phenotypes Associated with This Genotype
Genotype
MGI:4420999
Allelic
Composition
Tg(Camk2a-tTA)1Mmay/0
Tg(tetO-LRRK2*G2019S)E3Cai/0
Genetic
Background
involves: C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Tg(Camk2a-tTA)1Mmay mutation (8 available)
Tg(tetO-LRRK2*G2019S)E3Cai mutation (1 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
growth/size/body
• starting at 1 year, mice appear to gain less body weight than non-transgenic and Tg(tetO-LRRK2*G2019S)E3Cai single mutant mice, but are not different from Tg(Camk2a-tTA)1Mmay animals

behavior/neurological
N
• mice show normal performance in the rotarod test
• mice show significantly increased ambulatory activities starting at 12 months of age; at 12 months mice show a trend to increased rearing activities but this does not reach statistical significance

nervous system
N
• no significant changes in neuron counts are observed compared to non-transgenic controls at the frontal cortex or dorsal striatum in 6- or 20-month old mice
• no increase in reactive astrocytosis or microglial activation are detected in the striatum or cortex at 20 months
• no alpha-synuclein accumulation is observed in neurons at 20 months
• the Golgi complex is drastically altered in neurons at 1 month, appearing thinner and fragmented
• at 6 months fragmentation of the cis-Golgi apparatus is similar to that in LRRK2WT and A53T/LRRK2 neurons
• at 1 month, the medial/trans-Golgi in neurons is significantly altered
• brain homogenates moderately elevated levels of ubiquitinated proteins at 18 months compared to non-transgenic controls


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
04/16/2024
MGI 6.23
The Jackson Laboratory