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Symbol
Name
ID

Pgap2
post-GPI attachment to proteins 2
MGI:2385286

Phenotype annotations related to embryo

Darker colors indicate more annotations

Human Phenotypes	Decreased fetal movement
Disease(s) Associated with PGAP2	Decreased fetal movement
hyperphosphatasia with impaired intellectual development syndrome 3

Mouse Phenotypes		abnormal neural tube morphology	abnormal placenta morphology	abnormal trophoblast layer morphology	abnormal visceral yolk sac morphology
Availability	Mouse Genotype	abnormal neural tube morphology	abnormal placenta morphology	abnormal trophoblast layer morphology	abnormal visceral yolk sac morphology
	Pgap2^{tm1b(EUCOMM)Wtsi}/Pgap2^{tm1b(EUCOMM)Wtsi}
	Pgap2^clpex/Pgap2^{tm1a(EUCOMM)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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