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Symbol
Name
ID

Myl2
myosin, light polypeptide 2, regulatory, cardiac, slow
MGI:97272

Phenotype annotations related to mortality/aging

*	Aspects of the system are reported to show a normal phenotype.
	Darker colors indicate more annotations

Human Phenotypes	Sudden cardiac death
Disease(s) Associated with MYL2	Sudden cardiac death
hypertrophic cardiomyopathy 10

Mouse Phenotypes		mortality/aging	premature death	lethality throughout fetal growth and development, complete penetrance	preweaning lethality, complete penetrance
Availability	Mouse Genotype	mortality/aging	premature death		preweaning lethality, complete penetrance
	Myl2^tm1.1Chen/Myl2^tm1.1Chen	*
	Myl2^{tm1b(EUCOMM)Hmgu}/Myl2^{tm1b(EUCOMM)Hmgu}
	Myl2^tm2.1Chen/Myl2^tm2.1Chen
	Myl2^{tm1(Hand1)Tana}/Myl2⁺

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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