| Human Disease |
Cerebral Cavernous Malformations; CCM OMIM ID: 116860 |
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| Synonyms | Cavernous Angioma, Familial; Cavernous Angiomatous Malformations; CAM | |||||||||||||||||||||||||
| View all models | View ALL (3) 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 |
| Ccm2Gt(RRG051)Byg/Ccm2+ |
involves: 129P2/OlaHsd * C57BL/6J | J:105314 | View |
| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Krit1tm1Dmar/Krit1tm1Dmar |
B6.129-Krit1tm1Dmar | J:88138 | View |
| Krit1tm1Arte/Krit1tm1Arte Tg(Cdh5-cre/ERT2)1Rha/0 |
involves: C57BL/6 | J:177584 | 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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