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Symbol
Name
ID
Kmt2e
lysine (K)-specific methyltransferase 2E
MGI:1924825
Phenotype annotations related to endocrine/exocrine glands
Darker colors indicate more annotations
Human Phenotypes
Increased serum serotonin
Disease(s) Associated with KMT2E
autistic disorder

Mouse Phenotypes
small thymus
thymus hypoplasia
decreased thymocyte number
dilated seminal vesicle
Availability Mouse Genotype
Kmt2etm1.1Hjf/Kmt2etm1.1Hjf
Kmt2etm1Apa/Kmt2etm1Apa
Kmt2etm1.1Hjf/Kmt2e+

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
04/30/2024
MGI 6.23
The Jackson Laboratory