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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Tg(SNCA)OVX37Rwm
transgene insertion OVX37, Richard Wade-Martins
MGI:5544307
Summary 1 genotype
Jump to Allelic Composition Genetic Background Genotype ID
cx1
Sncatm1Rosl/Sncatm1Rosl
Tg(SNCA)OVX37Rwm/0
B6.Cg-Tg(SNCA)OVX37Rwm Sncatm1Rosl MGI:5544308


Genotype
MGI:5544308
cx1
Allelic
Composition
Sncatm1Rosl/Sncatm1Rosl
Tg(SNCA)OVX37Rwm/0
Genetic
Background
B6.Cg-Tg(SNCA)OVX37Rwm Sncatm1Rosl
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Sncatm1Rosl mutation (4 available); any Snca mutation (36 available)
Tg(SNCA)OVX37Rwm mutation (1 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
behavior/neurological
• 18 month old mutants show a reduced latency to fall on the rotarod test and are impaired on the multiple static rods test
• however, no differences in the latency to fall in the inverted screen test is seen
• reduction in forepaw stride length in 18 month old mutants

digestive/alimentary system
• dry stool weight is increased in males but not females, independent of age; however, stool frequency and stool water content are normal, indicating constipation-like phenotype

homeostasis/metabolism
• net dopamine content is unchanged in caudate putamen or nucleus accumbens at 3-4 and 12 months of age, however at 18 months of age, dopamine content is greater in the caudate putamen

nervous system
• vesicles in dopamine axons of the dorsal striatum are more clustered than in controls at 3 months of age; the frequency distribution of intervesicle distance is reduced and vesicles are 3 times less dispersed
• 18 month old mutants exhibit loss of substantia nigra pars compacta dopamine neurons
• 18 month old mutants exhibit loss of substantia nigra pars compacta dopamine neurons
• however, aggregation of alpha-synuclein is not seen in the substantia nigra pars compacta or striatum
• substantia nigra pars compacta dopamine neurons exhibit age-dependent reductions (almost 30%) in firing rates in vivo
• in the dorsal striatum, mean peak extracellular concentrations of dopamine evoked by single electrical pulses across distributed recording sites are on average about 30% lower than in controls; this reduced release is seen from a young age of 3-4 months before the loss of dopamine neurons and persists throughout their lifespan
• greatest deficits in dopamine release are seen in the dorsal and lateral striatum
• the dopamine release deficit persists in the presence of nicotinic receptor blockade by dihydro-beta-erythroidine
• dopamine uptake kinetics are normal and norepinephrine and 5-hydroxytryptamine axonal release are normal

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
Parkinson's disease 1 DOID:0060367 OMIM:168601
J:201991





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last database update
11/19/2024
MGI 6.24
The Jackson Laboratory