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Tg(Prnp-PFN1*C71G)22Zxu
Transgene Detail
Nomenclature
Symbol: Tg(Prnp-PFN1*C71G)22Zxu
Name: transgene insertion 22, Zuoshang Xu
MGI ID: MGI:5796267
Synonyms: Prp-PFN1C71G
Transgene: Tg(Prnp-PFN1*C71G)22Zxu  Location: unknown  
Transgene
origin
Strain of Origin:  FVB/N
Transgene
description
Transgene Type:    Transgenic (Humanized sequence, Inserted expressed sequence)
Mutation:    Insertion
 
Tg(Prnp-PFN1*C71G)22Zxu expresses 1 gene
 
Mutation detailsThe transgenic construct contains a mutant human profilin 1 cDNA sequence with a V5 tag (45 bp) fused to the N-terminus and inserted between exon 2 and exon 3 of mouse prion protein gene at a unique XhoI site in the MoPrP.Xho plasmid vector. PFN1 harbors the C71G mutation associated with amyotrophic lateral sclerosis (ALS). (J:235427)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Disease models
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Find Mice (IMSR)
Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:  Mouse Strains: 1 strain available      Cell Lines: 0 lines available
References
Original:  J:235427 Yang C, et al., Mutant PFN1 causes ALS phenotypes and progressive motor neuron degeneration in mice by a gain of toxicity. Proc Natl Acad Sci U S A. 2016 Sep 28;
All:  1 reference(s)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
01/09/2018
MGI 6.11
The Jackson Laboratory