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Symbol
Name
ID
Kmt2d
lysine (K)-specific methyltransferase 2D
MGI:2682319
Phenotype annotations related to nervous system
Darker colors indicate more annotations
Human Phenotypes
Microcephaly
Central hypotonia
Cerebral cortical atrophy
Hydrocephalus
Ventriculomegaly
EEG abnormality
Intellectual disability
Behavioral abnormality
Global developmental delay
Seizures
Disease(s) Associated with KMT2D
Kabuki syndrome

Mouse Phenotypes
abnormal dentate gyrus morphology
abnormal hippocampus granule cell layer
Availability Mouse Genotype
Kmt2dGt(RRT024)Byg/Kmt2d+

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
10/15/2019
MGI 6.14
The Jackson Laboratory