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Myogtm3Whk
Targeted Allele Detail
Summary
Symbol: Myogtm3Whk
Name: myogenin; targeted mutation 3, William H Klein
MGI ID: MGI:3618992
Synonyms: Myogflox
Gene: Myog  Location: Chr1:134217742-134220286 bp, + strand  Genetic Position: Chr1, 58.18 cM
Alliance: Myogtm3Whk page
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:105925
Parent Cell Line:  AB1 (ES Cell)
Strain of Origin:  129S7/SvEvBrd-Hprt1+
Mutation
description
Allele Type:    Targeted (Conditional ready, No functional change)
Mutation:    Insertion
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Structures Affected by this Mutation: 2 anatomical structure(s)
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 Myog Mutation:  14 strains or lines available
References
Original:  J:105925 Knapp JR, et al., Loss of myogenin in postnatal life leads to normal skeletal muscle but reduced body size. Development. 2006 Feb;133(4):601-10
All:  10 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
04/16/2024
MGI 6.23
The Jackson Laboratory