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Mbnl1em1Coop
Endonuclease-mediated Allele Detail
Summary
Symbol: Mbnl1em1Coop
Name: muscleblind like splicing regulator 1; endonuclease-mediated mutation 1, Thomas A Cooper
MGI ID: MGI:8350476
Synonyms: Mbnl1flox
Gene: Mbnl1  Location: Chr3:60380251-60537171 bp, + strand  Genetic Position: Chr3, 29.17 cM, cytoband E1
Alliance: Mbnl1em1Coop page
Mutation
origin
Strain of Origin:  C57BL/6NJ
Mutation
description
Allele Type:    Endonuclease-mediated (Conditional ready)
Mutation:    Insertion
 
Mutation detailsExon 3 (1,049 bp) that contains the translational start site was flanked by loxP sites via CRISPR/Cas9 mediated recombination. (J:386516)
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: 0 strains available      Cell Lines: 0 lines available
Carrying any Mbnl1 Mutation:  39 strains or lines available
References
Original:  J:386516 Peterson JAM, et al., MBNL loss of function in smooth muscle as a model for myotonic dystrophy associated gastrointestinal dysmotility. Proc Natl Acad Sci U S A. 2025 Dec 16;122(50):e2522788122
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
06/09/2026
MGI 6.24
The Jackson Laboratory