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Symbol
Name
ID
Pmm2
phosphomannomutase 2
MGI:1859214
Phenotype annotations related to mortality/aging
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
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

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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last database update
04/16/2024
MGI 6.23
The Jackson Laboratory