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Symbol
Name
ID
Kmt2a
lysine (K)-specific methyltransferase 2A
MGI:96995
Phenotype annotations related to liver/biliary system
Darker colors indicate more annotations
Human Phenotypes
Hepatomegaly
Disease(s) Associated with KMT2A
myelofibrosis

Mouse Phenotypes
abnormal liver development
liver hypoplasia
Availability Mouse Genotype
Kmt2atm1.1Brad/Kmt2atm1.1Brad
Kmt2atm1.1Mlc/Kmt2atm1.1Mlc

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
04/23/2024
MGI 6.23
The Jackson Laboratory