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Symbol Name ID |
Ehmt1
euchromatic histone methyltransferase 1 MGI:1924933 |
| Darker colors indicate more annotations |
| Human Phenotypes | Brachycephaly |
Mandibular prognathia |
Malar flattening |
Microcephaly |
Brachydactyly |
Limitation of joint mobility |
Scoliosis |
| Disease(s) Associated with EHMT1 | |||||||
| Kleefstra syndrome 1 |
| Mouse Phenotypes | abnormal metopic suture morphology |
malocclusion |
abnormal nasal bone morphology |
delayed intramembranous bone ossification |
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| Availability | Mouse Genotype | ||||
| Ehmt1tm1Bzhu/Ehmt1tm1Bzhu | |||||
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 05/28/2024 MGI 6.13 |
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