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Symbol Name ID |
Phgdh
3-phosphoglycerate dehydrogenase MGI:1355330 |
| Darker colors indicate more annotations |
| Human Phenotypes | Cataract |
Developmental cataract |
Hypertelorism |
Proptosis |
Microphthalmia |
Nystagmus |
| Disease(s) Associated with PHGDH | ||||||
| Neu-Laxova syndrome 1 | ||||||
| PHGDH deficiency |
| Mouse Phenotypes | abnormal eye morphology |
microphthalmia |
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| Availability | Mouse Genotype | ||
| Phgdhtm1b(KOMP)Wtsi/Phgdhtm1b(KOMP)Wtsi | |||
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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