Myl9 Phenotype Annotations

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Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Myl9
myosin, light polypeptide 9, regulatory
MGI:2138915

14 phenotypes from 2 alleles in 2 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Myl9^tm1.1Mzhu/Myl9^tm1.1Mzhu involves: BALB/cJ * C57BL/6	abnormal intestine morphology	J:308237
	decreased body size	J:308237
	distended urinary bladder	J:308237
	postnatal lethality, complete penetrance	J:308237
Myl9^tm1Mzhu/Myl9^tm1Mzhu Tg(Acta2-cre)#Xya/0 involves: C57BL/6 * CBA	abnormal aorta smooth muscle morphology	J:308237
	abnormal intestinal peristalsis	J:308237
	abnormal jejunum morphology	J:308237
	abnormal liver morphology	J:308237
	abnormal vascular smooth muscle physiology	J:308237
	distended duodenum	J:308237
	distended jejunum	J:308237
	impaired contractility of jejunal smooth muscle	J:308237
	impaired smooth muscle contractility	J:308237
	premature death	J:308237

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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