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Symbol Name ID |
Emg1
EMG1 N1-specific pseudouridine methyltransferase MGI:1315195 |
| Darker colors indicate more annotations |
| Human Phenotypes | Microcephaly |
Ventriculomegaly |
Severe global developmental delay |
Seizure |
| Disease(s) Associated with EMG1 | ||||
| Bowen-Conradi syndrome |
| Mouse Phenotypes | incomplete rostral neuropore closure |
open neural tube |
wavy neural tube |
abnormal telencephalon development |
exencephaly |
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| Availability | Mouse Genotype | |||||
| Emg1tm1.1Btr/Emg1tm1.1Btr | ||||||
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 04/23/2024 MGI 6.23 |
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