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Symbol Name ID |
Phgdh
3-phosphoglycerate dehydrogenase MGI:1355330 |
| Darker colors indicate more annotations |
| Human Phenotypes | Decreased fetal movement |
Fetal akinesia sequence |
| Disease(s) Associated with PHGDH | ||
| Neu-Laxova syndrome 1 |
| Mouse Phenotypes | decreased fluid intake |
decreased food intake |
unresponsive to tactile stimuli |
no spontaneous movement |
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| Availability | Mouse Genotype | ||||
| Phgdhtm1b(KOMP)Wtsi/Phgdh+ | |||||
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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