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Symbol Name ID |
Kmt2d
lysine (K)-specific methyltransferase 2D MGI:2682319 |
| Darker colors indicate more annotations |
| Human Phenotypes | Congenital diaphragmatic hernia |
Short stature |
Decreased body weight |
Failure to thrive |
Obesity |
Growth delay |
Intrauterine growth retardation |
Postnatal growth retardation |
| Disease(s) Associated with KMT2D | ||||||||
| Kabuki syndrome |
| Mouse Phenotypes | decreased body fat mass |
short nasal bone |
abnormal palatal shelf morphology |
broad face |
face hypoplasia |
cleft palate |
glossoptosis |
abnormal snout morphology |
flattened snout |
abnormal ear shape |
embryonic growth retardation |
decreased body weight |
decreased body length |
decreased susceptibility to diet-induced obesity |
decreased body size |
postnatal growth retardation |
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| Availability | Mouse Genotype | ||||||||||||||||
| Kmt2dGt(RRT024)Byg/Kmt2d+ | |||||||||||||||||
| Kmt2dtm1.1Kaig/Kmt2dtm1.1Kaig Mesp1tm2(cre)Ysa/Mesp1+ (conditional) |
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| H2az2Tg(Wnt1-cre)11Rth/H2az2+ Kmt2dtm2.1Kaig/Kmt2dtm2.1Kaig (conditional) |
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| Kmt2dtm2.1Kaig/Kmt2dtm2.1Kaig Tg(Sox10-cre)1Wdr/0 (conditional) |
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| H2az2Tg(Wnt1-cre)11Rth/H2az2+ Kmt2dtm2.1Kaig/Kmt2d+ (conditional) |
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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 |
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