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Myottm1.1Moza
Targeted Allele Detail
Summary
Symbol: Myottm1.1Moza
Name: myotilin; targeted mutation 1.1, Monica Moza
MGI ID: MGI:3697714
Synonyms: Myo-
Gene: Myot  Location: Chr18:44467141-44488791 bp, + strand  Genetic Position: Chr18, 23.74 cM, cytoband B3
Alliance: Myottm1.1Moza page
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:117709
Parent Cell Line:  R1 (ES Cell)
Strain of Origin:  (129X1/SvJ x 129S1/Sv)F1-Kitl+
Mutation
description
Allele Type:    Targeted (Null/knockout)
Mutation:    Intragenic deletion
 
Mutation detailsExon 3 was removed via cre-mediated recombination. Neither full length nor truncated protein was detected in mutants. (J:117709)
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 Myot Mutation:  28 strains or lines available
References
Original:  J:117709 Moza M, et al., Targeted deletion of the muscular dystrophy gene myotilin does not perturb muscle structure or function in mice. Mol Cell Biol. 2007 Jan;27(1):244-52
All:  2 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
03/12/2024
MGI 6.23
The Jackson Laboratory