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Phenotypes Associated with This Genotype
Genotype
MGI:5051641
Allelic
Composition
Nf2tm2Gth/Nf2tm2Gth
Ptgdstm1.1(cre)Gvn/Ptgds+
Genetic
Background
involves: 129P2/OlaHsd * FVB/N
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Nf2tm2Gth mutation (3 available); any Nf2 mutation (65 available)
Ptgdstm1.1(cre)Gvn mutation (0 available); any Ptgds mutation (17 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
endocrine/exocrine glands
• observed in 69% of mice examined

mortality/aging
N
• mice are born at normal Mendelian frequencies, are viable, and show comparable survival to control littermates (>75% survive to 10 months)

neoplasm
• observed in 69% of mice examined
• meningiomas are frequently observed; development is restricted to base of skull ventral to brainstem
• observed in 81% of mice examined

nervous system
• observed in 69% of mice examined
• meningiomas are frequently observed; development is restricted to base of skull ventral to brainstem

skeleton
• observed in 81% of mice examined


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
12/17/2024
MGI 6.24
The Jackson Laboratory