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Symbol
Name
ID

Kmt2d
lysine (K)-specific methyltransferase 2D
MGI:2682319

Phenotype annotations related to muscle

Darker colors indicate more annotations

Human Phenotypes	Congenital diaphragmatic hernia	Hypotonia	Generalized hypotonia
Disease(s) Associated with KMT2D
Kabuki syndrome

Mouse Phenotypes		thin myocardium compact layer	decreased fetal cardiomyocyte proliferation	abnormal muscle morphology	decreased muscle weight
Availability	Mouse Genotype	thin myocardium compact layer	decreased fetal cardiomyocyte proliferation	abnormal muscle morphology	decreased muscle weight
	Kmt2d^tm1.1Kaig/Kmt2d^tm1.1Kaig Myf5^tm3(cre)Sor/Myf5⁺ (conditional)
	Kmt2d^tm1.1Kaig/Kmt2d^tm1.1Kaig Tg(Tnnt2-cre)5Blh/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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