| Human Disease |
Cerebral Cavernous Malformations 2; CCM2 OMIM ID: 603284 |
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| View all models | View ALL (2) 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 |
| Ccm2tm2.1Sbn/Ccm2tm2.1Sbn Tg(Mx1-cre)1Cgn/0 |
involves: C57BL/6 * CBA | J:174085 | View |
| Ccm2tm1.1Etl/Ccm2tm1Etl Tg(Cdh5-cre/ERT2)1Rha/0 |
involves: 129 * C57BL/6 | J:177584 | View |
| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Ccm2tm1Etl/Ccm2tm1Etl Tg(Nes-cre)1Kln/? |
B6.Cg-Ccm2tm1Etl Tg(Nes-cre)1Kln | J:146210 | View |
| Ccm2tm2.1Sbn/Ccm2tm2.1Sbn Tg(Tek-cre)1Ywa/0 |
involves: C57BL/6 * SJL | J:174085 | View |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc |
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last database update 05/22/2013 MGI 5.13 |
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