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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID 		Myog
myogenin
MGI:97276
12 phenotypes from multigenic genotypes
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Allelic Composition
Genetic Background		 Annotated Term Reference
Myf6tm1Eno/Myf6tm1Eno
Myod1tm1Jae/Myod1+
Myogtm1Whk/Myog+
involves: 129S4/SvJae * 129S7/SvEvBrd * C57BL/6 		no abnormal phenotype detected J:48809
Myf6tm1Eno/Myf6tm1Eno
Myod1tm1Jae/Myod1tm1Jae
Myogtm1Whk/Myog+
involves: 129S4/SvJae * 129S7/SvEvBrd * C57BL/6 		abnormal myogenesis J:48809
Myf6tm1Eno/Myf6tm1Eno
Myod1tm1Jae/Myod1tm1Jae
Myogtm1Whk/Myogtm1Whk
involves: 129S4/SvJae * 129S7/SvEvBrd * C57BL/6 		abnormal muscle development J:61155
abnormal rib morphology J:61155
decreased fetal size J:61155
kyphosis J:61155
muscle hypoplasia J:61155
neonatal lethality, complete penetrance J:61155
Myf6tm1Eno/Myf6tm1Eno
Myogtm1Whk/Myogtm1Whk
involves: 129S7/SvEvBrd * C57BL/6 		abnormal muscle fiber morphology J:48809
abnormal sternebra morphology J:48809
abnormal sternocostal joint morphology J:48809
muscle hypoplasia J:48809
neonatal lethality, complete penetrance J:48809
split sternum J:48809
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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Send questions and comments to User Support. 		last database update
04/30/2024
MGI 6.23 		The Jackson Laboratory