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Symbol
Name
ID

Phgdh
3-phosphoglycerate dehydrogenase
MGI:1355330

Phenotype annotations related to embryo

Darker colors indicate more annotations

Human Phenotypes	Small placenta	Short umbilical cord	Polyhydramnios	Decreased fetal movement	Fetal akinesia sequence
Disease(s) Associated with PHGDH
Neu-Laxova syndrome 1

Mouse Phenotypes		abnormal vitelline vasculature morphology	abnormal embryo development	abnormal embryo turning	embryonic growth retardation	abnormal embryo size	decreased embryo size	abnormal embryonic neuroepithelial layer differentiation	abnormal visceral yolk sac morphology
Availability	Mouse Genotype	abnormal vitelline vasculature morphology	abnormal embryo development	abnormal embryo turning	embryonic growth retardation	abnormal embryo size	decreased embryo size	abnormal embryonic neuroepithelial layer differentiation	abnormal visceral yolk sac morphology
	Phgdh^tm1.1Shfu/Phgdh^tm1.1Shfu
	Phgdh^{tm1b(KOMP)Wtsi}/Phgdh^{tm1b(KOMP)Wtsi}

Contributing Projects: 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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