Symbol Name ID |
Emg1
EMG1 N1-specific pseudouridine methyltransferase MGI:1315195 |
Darker colors indicate more annotations |
Human Phenotypes | Feeding difficulties in infancy |
Disease(s) Associated with EMG1 | |
Bowen-Conradi syndrome |
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 04/30/2024 MGI 6.23 |
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