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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
Central hypotonia
Muscular 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
Kmt2dtm1.1Kaig/Kmt2dtm1.1Kaig
Myf5tm3(cre)Sor/Myf5+  (conditional)
Kmt2dtm1.1Kaig/Kmt2dtm1.1Kaig
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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last database update
09/10/2019
MGI 6.14
The Jackson Laboratory