| Human Disease |
Meningioma, Familial, Susceptibility to OMIM ID: 607174 |
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| View all models | View ALL (1) mouse models for this human disease. | |||||||||||||||||||||||||||||||||||||||||||
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Genes and mouse models |
Mutations in human and/or mouse homologs are associated with this disease
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| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Cdkn2atm1.1Brn/Cdkn2atm1.1Brn Nf2tm2Gth/Nf2tm2Gth |
involves: 129P2/OlaHsd * FVB/N | J:131179 | View |
| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Nf2tm1Tyj/Nf2+ |
either: (involves: 129S2/SvPas * 129S4/SvJae * C57BL/6) or (involves: 129S2/SvPas * C57BL/6J) | J:47282 | View |
| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Cdkn2atm1.1Brn/Cdkn2atm1.1Brn Nf2tm2Gth/Nf2tm2Gth |
involves: 129P2/OlaHsd * FVB/N | J:131179 | View |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc |
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last database update 05/08/2013 MGI 5.13 |
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