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Tg(Prnp-SNCA*A53T)25Mkle
Transgene Detail
Summary
Symbol: Tg(Prnp-SNCA*A53T)25Mkle
Name: transgene insertion 25, Michael K Lee
MGI ID: MGI:4942280
Synonyms: A53T, N2-5, Tg(Prnp-SNCA*A53T)BAub
Transgene: Tg(Prnp-SNCA*A53T)25Mkle  Location: unknown  
Alliance: Tg(Prnp-SNCA*A53T)25Mkle page
Transgene
origin
Strain of Origin:  (C3H/HeJ x C57BL/6J)F1
Transgene
description
Transgene Type:    Transgenic (Humanized sequence, Inserted expressed sequence)
Mutation:    Insertion
 
Tg(Prnp-SNCA*A53T)25Mkle expresses 1 gene
 
Mutation detailsThe transgene contains a human alpha synuclein cDNA encoding the Ala53Thr amino acid substitution, and the murine prion promoter. Lines G2-3, H5, and N2-5 were generated (J:77344)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Disease models
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Expression
In Structures Affected by this Mutation: 3 anatomical structure(s)
Find Mice (IMSR)
Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:  Mouse Strains: 0 strains available      Cell Lines: 0 lines available
References
Original:  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:  6 reference(s)

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)
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last database update
12/10/2024
MGI 6.24
The Jackson Laboratory