|
Symbol Name ID |
Ehmt1
euchromatic histone methyltransferase 1 MGI:1924933 |
| Darker colors indicate more annotations |
| Human Phenotypes | Hernia |
Short stature |
Obesity |
| Disease(s) Associated with EHMT1 | |||
| Kleefstra syndrome 1 |
| Mouse Phenotypes | malocclusion |
abnormal nasal bone morphology |
embryonic growth retardation |
decreased embryo weight |
decreased birth body size |
increased lean body mass |
increased body weight |
obese |
postnatal growth retardation |
decreased fetal weight |
prenatal growth retardation |
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| Availability | Mouse Genotype | |||||||||||
| Ehmt1tm1Bzhu/Ehmt1tm1Bzhu | ||||||||||||
| Ehmt1tm1Yshk/Ehmt1tm1Yshk | ||||||||||||
| Ehmt1tm1b(EUCOMM)Hmgu/Ehmt1+ | ||||||||||||
| Ehmt1tm1.1Tara/Ehmt1tm1.1Tara Tg(Camk2a-cre)2Gsc/0 (conditional) |
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| Ehmt1tm1.1Tara/Ehmt1tm1.1Tara Tg(Adipoq-cre)1Evdr/0 (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 06/04/2024 MGI 6.13 |
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