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Symbol Name ID |
Phgdh
3-phosphoglycerate dehydrogenase MGI:1355330 |
| Darker colors indicate more annotations |
| Human Phenotypes | Micrognathia |
Dandy-Walker malformation |
Primary microcephaly |
Sloping forehead |
Thick lower lip vermilion |
Cleft upper lip |
Swollen lip |
Cleft palate |
Depressed nasal ridge |
Wide nose |
Absent eyelashes |
Ablepharon |
| Disease(s) Associated with PHGDH | ||||||||||||
| Neu-Laxova syndrome 1 | ||||||||||||
| PHGDH deficiency |
| Mouse Phenotypes | abnormal head shape |
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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 04/09/2024 MGI 6.23 |
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