Mymx Phenotype Annotations

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Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Mymx
myomixer, myoblast fusion factor
MGI:3649059

13 phenotypes from 2 alleles in 1 genetic background

Allelic Composition Genetic Background	Annotated Term	Reference
Mymx^em1Shcs/Mymx^em1Shcs involves: C57BL/6J	abnormal intercostal muscle morphology	J:241564
	abnormal limb morphology	J:241564
	abnormal limb muscle morphology	J:241564
	abnormal muscle morphology	J:241564
	abnormal myoblast fusion	J:241564
	abnormal skeletal muscle morphology	J:241564
	abnormal spine curvature	J:241564
	cyanosis	J:241564
	decreased fetal weight	J:241564
	muscle weakness	J:241564
	neonatal lethality, complete penetrance	J:241564
	nuchal edema	J:241564
	primary atelectasis	J:241564
Mymx^em2Shcs/Mymx^em2Shcs involves: C57BL/6J	neonatal lethality, complete penetrance	J:241565

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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