Symbol Name ID |
Kmt2d
lysine (K)-specific methyltransferase 2D MGI:2682319 |
Darker colors indicate more annotations |
Human Phenotypes | Recurrent otitis media |
Conductive hearing impairment |
Low-set ears |
Posteriorly rotated ears |
Cupped ear |
Macrotia |
Protruding ear |
Sensorineural hearing impairment |
Hearing impairment |
Disease(s) Associated with KMT2D | |||||||||
Kabuki syndrome |
Mouse Phenotypes | abnormal ear shape |
abnormal inner ear canal morphology |
|
Availability | Mouse Genotype | ||
Kmt2dGt(RRT024)Byg/Kmt2d+ | |||
H2az2Tg(Wnt1-cre)11Rth/H2az2+ Kmt2dtm2.1Kaig/Kmt2d+ (conditional) |
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 05/14/2024 MGI 6.23 |
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