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Symbol
Name
ID
Kmt2c
lysine (K)-specific methyltransferase 2C
MGI:2444959
Phenotype annotations related to vision/eye
Darker colors indicate more annotations
Human Phenotypes
Developmental cataract
Hypermetropia
Disease(s) Associated with KMT2C
Kleefstra syndrome 2

Mouse Phenotypes
delayed eyelid opening
Availability Mouse Genotype
Kmt2ctm1.1Jwle/Kmt2ctm1.1Jwle

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
04/16/2024
MGI 6.23
The Jackson Laboratory