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B6.Cg-2310039L15RikTg(Prnp-SNCA*A53T)23Mkle/J Strain Detail
Summary
  • Strain Name
    B6.Cg-2310039L15RikTg(Prnp-SNCA*A53T)23Mkle/J
  • Attributes
    congenic, mutant strain, transgenic
  • MGI ID
    MGI:3797580
  • Synonyms
    B6.Cg-Tg(Prnp-SNCA*A53T)23Mkle/J
  • Other IDs
    JAX:006823
Associated
Mutations,
Markers,
and QTL
1 associated mutation
Find Mice (IMSR)
1 associated strain record at IMSR
IMSR Repository IMSR Strain Why Matched
JAX:006823 JAX B6.Cg-2310039L15RikTg(Prnp-SNCA*A53T)23Mkle/J exact match to ID
References
  • Earliest
    J:77344 Lee MK, et al., Human alpha-synuclein-harboring familial Parkinson's disease-linked Ala-53 --> Thr mutation causes neurodegenerative disease with alpha-synuclein aggregation in transgenic mice. Proc Natl Acad Sci U S A. 2002 Jun 25;99(13):8968-73
  • All
    17
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
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Send questions and comments to User Support. 		last database update
01/06/2026
MGI 6.24 		The Jackson Laboratory