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Symbol
Name
ID

Myl9
myosin, light polypeptide 9, regulatory
MGI:2138915

Phenotype annotations related to mortality/aging

Darker colors indicate more annotations

Human Phenotypes	Death in infancy
Disease(s) Associated with MYL9	Death in infancy
megacystis-microcolon-intestinal hypoperistalsis syndrome

Mouse Phenotypes		premature death	postnatal lethality, complete penetrance
Availability	Mouse Genotype	premature death	postnatal lethality, complete penetrance
	Myl9^tm1.1Mzhu/Myl9^tm1.1Mzhu
	Myl9^tm1Mzhu/Myl9^tm1Mzhu Tg(Acta2-cre)#Xya/0 (conditional)

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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