Symbol Name ID |
Kmt2d
lysine (K)-specific methyltransferase 2D MGI:2682319 |
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 |
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Availability | Mouse Genotype | ||||
Kmt2dtm1.1Kaig/Kmt2dtm1.1Kaig Myf5tm3(cre)Sor/Myf5+ (conditional) |
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Kmt2dtm1.1Kaig/Kmt2dtm1.1Kaig Tg(Tnnt2-cre)5Blh/0 (conditional) |
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 05/14/2024 MGI 6.23 |
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