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Symbol Name ID |
Gphn
gephyrin MGI:109602 |
| Darker colors indicate more annotations |
| Human Phenotypes | Neonatal death |
| Disease(s) Associated with GPHN | |
| molybdenum cofactor deficiency type C |
| Mouse Phenotypes | neonatal lethality, complete penetrance |
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| Availability | Mouse Genotype | |
| Gphntm1Jrs/Gphntm1Jrs | ||
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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