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| Nomenclature |
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Symbol:
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Myottm1.1Moza
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Name:
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myotilin;
targeted mutation 1.1, Monica Moza
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MGI ID: |
MGI:3697714 |
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Synonyms: |
Myo- |
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Gene:
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Myot
Location:
Chr18:44334074-44355724 bp, + strand
Genetic Position: Chr18,
23.74 cM, cytoband B3
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Mutation
origin |
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Germline Transmission:
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Earliest citation of germline transmission:
J:117709
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Parent Cell Line:
| R1 (ES Cell) |
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Strain of Origin:
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(129X1/SvJ x 129S1/Sv)F1-Kitl+
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Mutation
description |
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Allele
Type: | |
Targeted (knock-out) |
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Mutation: | |
Intragenic deletion |
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Mutation details: Exon 3 was removed via cre-mediated recombination. Neither full length nor truncated protein was detected in mutants. (J:117709)
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Phenotypes
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View phenotypes for all genotypes (concatenated display).
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Disease models
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| Find Mice (IMSR) |
Mouse strains and cell lines available from the
International Mouse Strain Resource
(IMSR)
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Carrying this Mutation: |
Mouse Strains: 0 strains available
Cell Lines: 0 lines available |
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Carrying any Myot Mutation:
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4 strains or lines available |
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| References |
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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
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All: |
1 reference(s)
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Analysis Tools
