About   Help   FAQ
Phenotypes Associated with This Genotype
Genotype
MGI:2681434
Allelic
Composition
Prkntm1Shn/Prkntm1Shn
Genetic
Background
involves: 129S4/SvJae
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Prkntm1Shn mutation (3 available); any Prkn mutation (53 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
behavior/neurological
• poorer performance in various measures of motor performance
• rotarod performance was normal

nervous system
• higher currents are required in striatal neurons to trigger synaptic response

homeostasis/metabolism
• higher than normal levels of dopamine in the striatum

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
Parkinson's disease 2 DOID:0060368 OMIM:600116
J:86377


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
09/03/2024
MGI 6.24
The Jackson Laboratory