Mymx Phenotype Annotations

Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Mymx
myomixer, myoblast fusion factor
MGI:3649059

23 phenotypes from 3 alleles in 2 genetic backgrounds

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
Mymx^em3Eno/Mymx^em3Eno involves: C57BL/6N	abnormal muscle fiber morphology	J:372295
	abnormal myoblast fusion	J:372295
	abnormal sarcomere morphology	J:372295
	absent gastric milk in neonates	J:372295
	decreased skeletal muscle size	J:372295
	hypoxia	J:372295
	neonatal lethality, incomplete penetrance	J:372295
	postnatal growth retardation	J:372295
	postnatal lethality, complete penetrance	J:372295
	respiratory failure	J:372295
	skeletal muscle fiber degeneration	J:372295

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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