32 phenotypes from multigenic genotypes

Allelic Composition Genetic Background	Annotated Term	Reference
Abl1tm1Gcos/Abl1+ Myf5tm2Tajb/Myf5tm2Tajb Myf6tm1Tajb/Myf6tm1Tajb Myod1tm2.1(icre)Glh/Myod1+ involves: 129S * 129X1/SvJ * C57BL/6J	abnormal myogenesis	J:168843
	decreased physiological sensitivity to xenobiotic	J:168843
Acvr1tm1Glh/Acvr1+ Myod1tm2.1(icre)Glh/Myod1+ involves: 129S6/SvEvTac * C57BL/6J * FVB/N	normal skeleton phenotype	J:257905
Dmdmdx/? Myod1tm1Jae/Myod1tm1Jae involves: 129S4/SvJae * C57BL/10ScSn	abnormal heart ventricle morphology	J:52248
	cardiac fibrosis	J:52248
	cardiac interstitial fibrosis	J:52248
	dilated cardiomyopathy	J:52248
	increased heart weight	J:52248
	increased myocardial fiber size	J:52248
	myocardium necrosis	J:52248
	premature death	J:52248
Fgf6tm1Thbr/Fgf6tm1Thbr Myod1tm1Jae/Myod1tm1Jae either: (involves: 129S4/SvJae) or (involves: 129S4/SvJae * C57BL/6)	decreased litter size	J:42574
Krastm4Tyj/Kras+ Myod1tm1.1(cre/ERT,TVA)Gcg/Myod1+ Trp53tm1Brn/Trp53tm1Brn involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6	increased sarcoma incidence	J:205518
	increased tumor incidence	J:205518
Myf5tm1(cre)Mrc/Myf5+ Myod1tm1Jae/Myod1tm1Jae Pax7tm1.1Thbr/Pax7tm1.1Thbr involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ	decreased satellite cell number	J:202693
Myf5tm1Jae/Myf5tm1Jae Myod1tm1.1Glh/Myod1+ involves: 129/Sv * 129S4/SvJae * C57BL/6J	abnormal muscle development	J:87370
Myf5tm1Jae/Myf5tm1Jae Myod1tm1.1Glh/Myod1tm1.1Glh involves: 129/Sv * 129S4/SvJae * C57BL/6J	abnormal muscle development	J:87370
Myf5tm1Pas/Myf5+ Myod1tm1Jae/Myod1tm1Jae involves: 129 * C57BL/6 * DBA/2	postnatal lethality	J:92799
Myf5tm1Pas/Myf5tm1Pas Myod1tm1Jae/Myod1+ involves: 129 * C57BL/6 * DBA/2	postnatal lethality	J:92799
Myf5tm1Pas/Myf5tm1Pas Myod1tm1Jae/Myod1tm1Jae involves: 129 * C57BL/6 * DBA/2	abnormal myogenesis	J:92799
	absent skeletal muscle	J:92799
	postnatal lethality, complete penetrance	J:92799
Myf5tm1Tajb/Myf5tm1Tajb Myod1tm1Jae/Myod1tm1Jae involves: 129/Sv * C57BL/6 * DBA/2	abnormal myogenesis	J:92799
	absent skeletal muscle	J:92799
	postnatal lethality, complete penetrance	J:92799
Myf5tm2Tajb/Myf5tm2Tajb Myod1tm1Jae/Myod1tm1Jae involves: 129/Sv * C57BL/6 * DBA/2	abnormal myogenesis	J:92799
	absent skeletal muscle	J:92799
	postnatal lethality, complete penetrance	J:92799
Myf5tm3(cre)Sor/Myf5tm3(cre)Sor Myod1tm1Jae/Myod1tm1Jae involves: 129S4/SvJae * C57BL/6J	abnormal myogenesis	J:65301
	abnormal myotube morphology	J:65301
Myf5tm4(Myod1)Sor/Myf5tm4(Myod1)Sor involves: 129S4/SvJae * C57BL/6J	normal muscle phenotype	J:65301
	normal skeleton phenotype	J:65301
Myf6tm1Eno/Myf6tm1Eno Myod1tm1Jae/Myod1+ Myogtm1Whk/Myog+ involves: 129S4/SvJae * 129S7/SvEvBrd * C57BL/6	no abnormal phenotype detected	J:48809
Myf6tm1Eno/Myf6tm1Eno Myod1tm1Jae/Myod1tm1Jae involves: 129S4/SvJae * 129S7/SvEvBrd * C57BL/6	abnormal adipose tissue distribution	J:48809
	abnormal rib morphology	J:48809
	absent skeletal muscle	J:48809
	centrally nucleated skeletal muscle fibers	J:48809
	decreased body size	J:48809
	decreased skeletal muscle fiber number	J:48809
	kyphosis	J:48809
	neonatal lethality, complete penetrance	J:48809
	respiratory failure	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