Msc Phenotype Annotations - Multigenic Genotypes

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Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Msc
musculin
MGI:1333884

12 phenotypes from multigenic genotypes

Allelic Composition Genetic Background	Annotated Term	Reference
Msc^tm1Eno/Msc⁺ Tcf21^tm2Eno/Tcf21^tm2Eno involves: 129 * Black Swiss	normal muscle phenotype	J:111337
Msc^tm1Eno/Msc^tm1Eno Tcf21^tm2Eno/Tcf21⁺ involves: 129 * Black Swiss	no abnormal phenotype detected	J:111337
Msc^tm1Eno/Msc^tm1Eno Tcf21^tm2Eno/Tcf21^tm2Eno involves: 129 * Black Swiss	abnormal masticatory muscle morphology	J:111337
	abnormal myogenesis	J:111337
	abnormal palatal shelf elevation	J:111337
	abnormal pterygoid muscle morphology	J:111337
	absent masseter muscle	J:111337
	absent pterygoid muscle	J:111337
	absent temporalis muscle	J:111337
	cleft secondary palate	J:111337
	diaphragmatic hernia	J:111337
	neonatal lethality, complete penetrance	J:111337

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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