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Tg(Prnp-ATXN7*92Q)1963Als
Transgene Detail
Summary
Symbol: Tg(Prnp-ATXN7*92Q)1963Als
Name: transgene insertion 1963, Albert R La Spada
MGI ID: MGI:5705123
Synonyms: Sca7
Transgene: Tg(Prnp-ATXN7*92Q)1963Als  Location: unknown  
Alliance: Tg(Prnp-ATXN7*92Q)1963Als page
Transgene
origin
Strain of Origin:  (C57BL/6J x C3H/HeJ)F1
Transgene
description
Transgene Type:    Transgenic (Humanized sequence, Inserted expressed sequence)
Mutation:    Insertion
 
Tg(Prnp-ATXN7*92Q)1963Als expresses 1 gene
 
Mutation detailsThe coding region of the human gene containing 92 CAG repeats is under the control of the murine prion protein promoter. N-terminal FLAG and C-terminal c-myc epitope tags were also added. Western blot analysis confirmed the expression of the full-length protein in the cerebellum and retina. (J:222402)
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:222402 Guyenet SJ, et al., Proteolytic cleavage of ataxin-7 promotes SCA7 retinal degeneration and neurological dysfunction. Hum Mol Genet. 2015 Jul 15;24(14):3908-17
All:  1 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