About   Help   FAQ
Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Myog
myogenin
MGI:97276
12 phenotypes from multigenic genotypes
Export: Excel File
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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support.
last database update
11/12/2024
MGI 6.24
The Jackson Laboratory