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Symbol
Name
ID
Kmt2d
lysine (K)-specific methyltransferase 2D
MGI:2682319
Phenotype annotations related to growth/size/body
Darker colors indicate more annotations
Human Phenotypes
Congenital diaphragmatic hernia
Short stature
Decreased body weight
Failure to thrive
Obesity
Growth delay
Intrauterine growth retardation
Postnatal growth retardation
Disease(s) Associated with KMT2D
Kabuki syndrome

Mouse Phenotypes
flattened snout
embryonic growth retardation
decreased body weight
Availability Mouse Genotype
Kmt2dGt(RRT024)Byg/Kmt2d+
Kmt2dtm1.1Kaig/Kmt2dtm1.1Kaig
Mesp1tm2(cre)Ysa/Mesp1+  (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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Funding Information
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last database update
09/10/2019
MGI 6.14
The Jackson Laboratory