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Wrnem1Cya
Endonuclease-mediated Allele Detail
Summary
Symbol: Wrnem1Cya
Name: Werner syndrome RecQ like helicase; endonuclease-mediated mutation 1, Cyagen Biosciences
MGI ID: MGI:7587578
Synonyms: Wrnem1
Gene: Wrn  Location: Chr8:33724412-33875555 bp, - strand  Genetic Position: Chr8, 20.3 cM, cytoband A4
Alliance: Wrnem1Cya page
Mutation
origin
Strain of Origin:  C57BL/6J
Mutation
description
Allele Type:    Endonuclease-mediated (Null/knockout)
Mutation:    Intragenic deletion
    Exon 9~10 will be selected as target site. (J:326541)
Inheritance:    Not Specified
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
Carrying any Wrn Mutation:  93 strains or lines available
References
Original:  J:326541 Cyagen Biosciences Inc., Cyagen Biosciences Website. 2022;
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
01/20/2026
MGI 6.24
The Jackson Laboratory