Myl7 Phenotype Annotations

Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Myl7
myosin, light polypeptide 7, regulatory
MGI:107495

20 phenotypes from 1 allele in 1 genetic background

Allelic Composition Genetic Background	Annotated Term	Reference
Myl7^tm1(cre)Krc/Myl7^tm1(cre)Krc involves: 129S1/Sv * 129X1/SvJ * Black Swiss	abnormal atrioventricular cushion morphology	J:87043
	abnormal cardiac epithelial to mesenchymal transition	J:87043
	abnormal cardiac outflow tract development	J:87043
	abnormal heart looping	J:87043
	abnormal heart rate	J:87043
	abnormal heart tube morphology	J:87043
	abnormal intersomitic vessel morphology	J:87043
	abnormal myocardial fiber morphology	J:87043
	abnormal vasculogenesis	J:87043
	abnormal visceral yolk sac morphology	J:87043
	abnormal vitelline vascular remodeling	J:87043
	absent vitelline blood vessels	J:87043
	dilated heart left ventricle	J:87043
	embryonic growth arrest	J:87043
	embryonic growth retardation	J:87043
	embryonic lethality during organogenesis, complete penetrance	J:87043
	increased heart atrium size	J:87043
	pericardial edema	J:87043
	trabecula carnea hypoplasia	J:87043
	ventricle myocardium hypoplasia	J:87043

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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