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Tg(Prnp-ATXN7*92Q)6529Als
Transgene Detail
Summary
Symbol: Tg(Prnp-ATXN7*92Q)6529Als
Name: transgene insertion 6529, Albert R La Spada
MGI ID: MGI:5704405
Synonyms: PrP-SCA7-c92Q
Transgene: Tg(Prnp-ATXN7*92Q)6529Als  Location: unknown  Genetic Position: ChrX, Syntenic
Alliance: Tg(Prnp-ATXN7*92Q)6529Als 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)6529Als expresses 1 gene
 
Mutation detailsThe coding region of human ATXN7, containing 92 CAG repeats is under the control of the murine prion protein promoter. This line integrated into the X chromosome and is a low expressor. (J:71971, J:135615)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
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:71971 La Spada AR, et al., Polyglutamine-expanded ataxin-7 antagonizes crx function and induces cone-rod dystrophy in a mouse model of sca7. (Erratum: Neuron 2001;32:957). Neuron. 2001 Sep 27;31(6):913-27
All:  3 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
04/16/2024
MGI 6.23
The Jackson Laboratory