About   Help   FAQ
Phenotypes Associated with This Genotype
Genotype
MGI:3720759
Allelic
Composition
Sncatm1Rosl/Sncatm1Rosl
Genetic
Background
involves: 129X1/SvJ * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Sncatm1Rosl mutation (4 available); any Snca mutation (36 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• when exposed to paired electrical stimuli, striatal brain slices (containing dopamine terminals) from homozygous mice exhibit a faster dopamine release recovery as compared to wild-type
• dopamine discharge and reuptake in response to a single electrical pulse or a train of pulses is comparable to wild-type

behavior/neurological
• homozygous mice exhibit an attenuated locomotor response after administration of amphetamine as compared to wild-type
• in the absence of amphetamine, locomotor activity in the open field test is comparable to wild-type

homeostasis/metabolism
• dopamine content is reduced by 18% in the striatum, however, dopamine content in the ventral midbrain and nucleus accumbens is similar to wild-type

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
Parkinson's disease 1 DOID:0060367 OMIM:168601
J:60151


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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support.
last database update
12/10/2024
MGI 6.24
The Jackson Laboratory