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Symbol
Name
ID

Pmm2
phosphomannomutase 2
MGI:1859214

Phenotype annotations related to embryo

*	Aspects of the system are reported to show a normal phenotype.
	Darker colors indicate more annotations

Human Phenotypes	Nonimmune hydrops fetalis	Abnormality of the amniotic fluid
Disease(s) Associated with PMM2	Nonimmune hydrops fetalis	Abnormality of the amniotic fluid
congenital disorder of glycosylation Ia

Mouse Phenotypes		embryo phenotype	embryonic growth retardation	abnormal embryonic tissue morphology	abnormal head mesenchyme morphology	abnormal embryonic neuroepithelium morphology	abnormal trophoblast giant cell morphology	abnormal extraembryonic tissue morphology
Availability	Mouse Genotype
	Pmm2^tm1.1Cknr/Pmm2^tm2.1Cknr	*

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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