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Symbol
Name
ID

Pmm2
phosphomannomutase 2
MGI:1859214

Phenotype annotations related to cardiovascular system

Darker colors indicate more annotations

Human Phenotypes	Intracranial hemorrhage	Cardiomyopathy	Hypertrophic cardiomyopathy	Pericardial effusion	Pericarditis	Stroke-like episode	Angina pectoris
Disease(s) Associated with PMM2
congenital disorder of glycosylation Ia

Mouse Phenotypes		abnormal myocardium layer morphology	abnormal myocardial fiber morphology	thin interventricular septum	thin ventricular wall	hemorrhage
Availability	Mouse Genotype	abnormal myocardium layer morphology	abnormal myocardial fiber morphology	thin interventricular septum	thin ventricular wall	hemorrhage
	Pmm2^tm1.1Cknr/Pmm2^tm2.1Cknr
	Pmm2^tm1.1Jins/Pmm2^tm2.1Jins

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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