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Symbol
Name
ID

Pomt2
protein-O-mannosyltransferase 2
MGI:2444430

Phenotype annotations related to mortality/aging

Darker colors indicate more annotations

Human Phenotypes	Death in infancy
Disease(s) Associated with POMT2	Death in infancy
congenital muscular dystrophy-dystroglycanopathy type A2

Mouse Phenotypes		embryonic lethality during organogenesis, complete penetrance	embryonic lethality before implantation, complete penetrance
Availability	Mouse Genotype
	Pomt2^tm1.2Hhu/Pomt2^tm1.2Hhu
	Pomt2^tm1Sstr/Pomt2^tm1Sstr

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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