Symbol Name ID |
Pomt2
protein-O-mannosyltransferase 2 MGI:2444430 |
Darker colors indicate more annotations |
Human Phenotypes | Death in infancy |
Disease(s) Associated with POMT2 | |
congenital muscular dystrophy-dystroglycanopathy type A2 |
Mouse Phenotypes | embryonic lethality during organogenesis, complete penetrance |
embryonic lethality before implantation, complete penetrance |
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Availability | Mouse Genotype | ||
Pomt2tm1.2Hhu/Pomt2tm1.2Hhu | |||
Pomt2tm1Sstr/Pomt2tm1Sstr |
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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last database update 04/16/2024 MGI 6.23 |
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