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Symbol
Name
ID

Mef2c
myocyte enhancer factor 2C
MGI:99458

Phenotype annotations related to muscle

Darker colors indicate more annotations

Human Phenotypes	Hypotonia
Disease(s) Associated with MEF2C	Hypotonia
neurodevelopmental disorder with hypotonia, stereotypic hand movements, and impaired language

Mouse Phenotypes		increased sinoatrial node size	trabecula carnea hypoplasia	dilated cardiomyopathy	decreased cardiac muscle contractility	decreased ventricle muscle contractility	abnormal skeletal muscle fiber type ratio
Availability	Mouse Genotype	increased sinoatrial node size	trabecula carnea hypoplasia	dilated cardiomyopathy	decreased cardiac muscle contractility	decreased ventricle muscle contractility	abnormal skeletal muscle fiber type ratio
	Mef2c^tm1.1Jjs/Mef2c^tm1.1Jjs
	Mef2c^tm1Eno/Mef2c^tm1Eno
	Tg(Myh6-Mef2c)2Jmol/0
	Tg(Myh6-Mef2c/VP16)1Eno/0
	Mef2c^tm1Eno/Mef2c^tm2Eno Tg(Myog-cre)1Eno/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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