Mymx Phenotype Annotations

About Help FAQ

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)
Citing These Resources Funding Information Warranty Disclaimer, Privacy Notice, Licensing, & Copyright Send questions and comments to User Support.	last database update 08/02/2024 MGI 6.24