Symbol Name ID |
Pmm2
phosphomannomutase 2 MGI:1859214 |
Darker colors indicate more annotations |
Human Phenotypes | Death in childhood |
Death in infancy |
Disease(s) Associated with PMM2 | ||
congenital disorder of glycosylation Ia |
Mouse Phenotypes | premature death |
embryonic lethality during organogenesis, complete penetrance |
embryonic lethality prior to tooth bud stage |
embryonic lethality prior to organogenesis |
embryonic lethality, complete penetrance |
prenatal lethality, complete penetrance |
prenatal lethality, incomplete penetrance |
preweaning lethality, complete penetrance |
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Availability | Mouse Genotype | ||||||||
Pmm2tm1.1Jins/Pmm2tm1.1Jins | |||||||||
Pmm2tm1b(EUCOMM)Hmgu/Pmm2tm1b(EUCOMM)Hmgu | |||||||||
Pmm2tm1Cthl/Pmm2tm1Cthl | |||||||||
Pmm2tm2.1Cknr/Pmm2tm2.1Cknr | |||||||||
Pmm2tm2.1Jins/Pmm2tm2.1Jins | |||||||||
Pmm2tm1.1Cknr/Pmm2tm2.1Cknr | |||||||||
Pmm2tm1.1Jins/Pmm2tm2.1Jins |
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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