Myod1 Phenotype Annotations - Multigenic Genotypes

Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Myod1
myogenic differentiation 1
MGI:97275

32 phenotypes from multigenic genotypes

Allelic Composition Genetic Background	Annotated Term	Reference
Abl1^tm1Gcos/Abl1⁺ Myf5^tm2Tajb/Myf5^tm2Tajb Myf6^tm1Tajb/Myf6^tm1Tajb Myod1^{tm2.1(icre)Glh}/Myod1⁺ involves: 129S * 129X1/SvJ * C57BL/6J	abnormal myogenesis	J:168843
	decreased physiological sensitivity to xenobiotic	J:168843
Acvr1^tm1Glh/Acvr1⁺ Myod1^{tm2.1(icre)Glh}/Myod1⁺ involves: 129S6/SvEvTac * C57BL/6J * FVB/N	normal skeleton phenotype	J:257905
Dmd^mdx/? Myod1^tm1Jae/Myod1^tm1Jae 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
Fgf6^tm1Thbr/Fgf6^tm1Thbr Myod1^tm1Jae/Myod1^tm1Jae either: (involves: 129S4/SvJae) or (involves: 129S4/SvJae * C57BL/6)	decreased litter size	J:42574
Kras^tm4Tyj/Kras⁺ Myod1^{tm1.1(cre/ERT,TVA)Gcg}/Myod1⁺ Trp53^tm1Brn/Trp53^tm1Brn involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6	increased sarcoma incidence	J:205518
	increased tumor incidence	J:205518
Myf5^tm1(cre)Mrc/Myf5⁺ Myod1^tm1Jae/Myod1^tm1Jae Pax7^tm1.1Thbr/Pax7^tm1.1Thbr involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ	decreased satellite cell number	J:202693
Myf5^tm1Jae/Myf5^tm1Jae Myod1^tm1.1Glh/Myod1⁺ involves: 129/Sv * 129S4/SvJae * C57BL/6J	abnormal muscle development	J:87370
Myf5^tm1Jae/Myf5^tm1Jae Myod1^tm1.1Glh/Myod1^tm1.1Glh involves: 129/Sv * 129S4/SvJae * C57BL/6J	abnormal muscle development	J:87370
Myf5^tm1Pas/Myf5⁺ Myod1^tm1Jae/Myod1^tm1Jae involves: 129 * C57BL/6 * DBA/2	postnatal lethality	J:92799
Myf5^tm1Pas/Myf5^tm1Pas Myod1^tm1Jae/Myod1⁺ involves: 129 * C57BL/6 * DBA/2	postnatal lethality	J:92799
Myf5^tm1Pas/Myf5^tm1Pas Myod1^tm1Jae/Myod1^tm1Jae involves: 129 * C57BL/6 * DBA/2	abnormal myogenesis	J:92799
	absent skeletal muscle	J:92799
	postnatal lethality, complete penetrance	J:92799
Myf5^tm1Tajb/Myf5^tm1Tajb Myod1^tm1Jae/Myod1^tm1Jae involves: 129/Sv * C57BL/6 * DBA/2	abnormal myogenesis	J:92799
	absent skeletal muscle	J:92799
	postnatal lethality, complete penetrance	J:92799
Myf5^tm2Tajb/Myf5^tm2Tajb Myod1^tm1Jae/Myod1^tm1Jae involves: 129/Sv * C57BL/6 * DBA/2	abnormal myogenesis	J:92799
	absent skeletal muscle	J:92799
	postnatal lethality, complete penetrance	J:92799
Myf5^tm3(cre)Sor/Myf5^tm3(cre)Sor Myod1^tm1Jae/Myod1^tm1Jae involves: 129S4/SvJae * C57BL/6J	abnormal myogenesis	J:65301
	abnormal myotube morphology	J:65301
Myf5^{tm4(Myod1)Sor}/Myf5^{tm4(Myod1)Sor} involves: 129S4/SvJae * C57BL/6J	normal muscle phenotype	J:65301
	normal skeleton phenotype	J:65301
Myf6^tm1Eno/Myf6^tm1Eno Myod1^tm1Jae/Myod1⁺ Myog^tm1Whk/Myog⁺ involves: 129S4/SvJae * 129S7/SvEvBrd * C57BL/6	no abnormal phenotype detected	J:48809
Myf6^tm1Eno/Myf6^tm1Eno Myod1^tm1Jae/Myod1^tm1Jae 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
Myf6^tm1Eno/Myf6^tm1Eno Myod1^tm1Jae/Myod1^tm1Jae Myog^tm1Whk/Myog⁺ involves: 129S4/SvJae * 129S7/SvEvBrd * C57BL/6	abnormal myogenesis	J:48809
Myf6^tm1Eno/Myf6^tm1Eno Myod1^tm1Jae/Myod1^tm1Jae Myog^tm1Whk/Myog^tm1Whk 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

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