About   Help   FAQ
Phenotypes Associated with This Genotype
Genotype
MGI:3814328
Allelic
Composition
Prkntm1Ykt/Prkntm1Ykt
Tg(PDGFB-GPR37)20Ryot/0
Genetic
Background
involves: 129P2/OlaHsd * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Prkntm1Ykt mutation (0 available); any Prkn mutation (27 available)
Tg(PDGFB-GPR37)20Ryot mutation (0 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• at 18 months of age, mice exhibit a reduction in the number of TH+ or Nissl staining neurons in the substantia nigra pars compacta and locus ceruleus associated with apoptosis

behavior/neurological
N
• mice exhibit normal behaviors

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
autosomal recessive juvenile Parkinson's disease 2 DOID:0060368 OMIM:600116
J:140326


Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
Citing These Resources
Funding Information
Warranty Disclaimer & Copyright Notice
Send questions and comments to User Support.
last database update
10/09/2018
MGI 6.12
The Jackson Laboratory