Phenotypes for Myog MGI:3656058 MGI Mouse

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Phenotypes Associated with This Genotype

Allelic Composition	Myog^tm1Whk/Myog^tm2Whk
Genetic Background	involves: 129S7/SvEvBrd * C57BL/6

Find Mice

Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Myog^tm1Whk mutation (0 available); any Myog mutation (13 available)
Myog^tm2Whk mutation (0 available); any Myog mutation (13 available)

♀	phenotype observed in females
♂	phenotype observed in males
N	normal phenotype

mortality/aging

neonatal lethality, complete penetrance ( J:54065 )

• die at birth

homeostasis/metabolism

edema ( J:54065 )

muscle

muscle hypoplasia ( J:54065 )

• severe

skeleton

abnormal sternum morphology ( J:54065 )

• fused and ossified

kyphosis ( J:54065 )

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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