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Symbol
Name
ID
Kmt2d
lysine (K)-specific methyltransferase 2D
MGI:2682319
Phenotype annotations related to behavior/neurological
Darker colors indicate more annotations
Human Phenotypes
Feeding difficulties
Feeding difficulties in infancy
Behavioral abnormality
Disease(s) Associated with KMT2D
Kabuki syndrome

Mouse Phenotypes
impaired contextual conditioning behavior
abnormal object recognition memory
impaired spatial learning
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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Funding Information
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last database update
09/05/2019
MGI 6.14
The Jackson Laboratory