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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Tg(PDGFB-LRRK2*G2019S)32Hlw
transgene insertion 32, Hung-Li Wang
MGI:5559903
Summary 1 genotype
Jump to Allelic Composition Genetic Background Genotype ID
tg1
Tg(PDGFB-LRRK2*G2019S)32Hlw/? FVB/N-Tg(PDGFB-LRRK2*G2019S)32Hlw MGI:5559904


Genotype
MGI:5559904
tg1
Allelic
Composition
Tg(PDGFB-LRRK2*G2019S)32Hlw/?
Genetic
Background
FVB/N-Tg(PDGFB-LRRK2*G2019S)32Hlw
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
behavior/neurological
• 12 month old mice show a reduction in spontaneous ambulatory activity and are less active
• 12 month old mice treated with methyl L-DOPA show rescue of hypoactivity
• 12 and 16 month old mice show an increase in the time required to perform the pole test, indicating impaired motor performance and bradykinesia

nervous system
• progressive degeneration of substantia nigra pars compacta dopaminergic neurons starting around 12 months of age
• mice show accumulation of hyperphosphorylated microtubule-associated protein tau in the brain at 12 months of age
• however, Lewy bodies or Lewy neurites are not seen in the substantia nigra
• striatal uptake of a tracer of presynaptic dopamine transporter is decreased in 12 month old mice and density of TH-immunoreactive staining is decreased in striatal sections indicating degeneration of nigrostriatal dopaminergic terminals
• progressive degeneration of substantia nigra pars compacta dopaminergic neurons starting around 12 months of age
• however, neuronal death is not seen in the cerebral cortex, hippocampus or striatum at 12 or 16 months of age

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
Parkinson's disease 8 DOID:0060371 OMIM:607060
J:204793





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last database update
11/05/2024
MGI 6.24
The Jackson Laboratory