Symbol Name ID |
Phgdh
3-phosphoglycerate dehydrogenase MGI:1355330 |
Darker colors indicate more annotations |
Human Phenotypes | Broad neck |
Short neck |
Growth delay |
Intrauterine growth retardation |
Disease(s) Associated with PHGDH | ||||
Neu-Laxova syndrome 1 | ||||
PHGDH deficiency |
Mouse Phenotypes | abnormal head shape |
embryonic growth retardation |
abnormal embryo size |
decreased embryo size |
abnormal head size |
microcephaly |
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Availability | Mouse Genotype | ||||||
Phgdhtm1.1Shfu/Phgdhtm1.1Shfu | |||||||
Phgdhtm1b(KOMP)Wtsi/Phgdhtm1b(KOMP)Wtsi | |||||||
Phgdhtm1.2Shfu/Phgdhtm1.2Shfu Tg(GFAP-cre)25Mes/0 (conditional) |
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 05/14/2024 MGI 6.23 |
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