| Human Disease |
Cardiofaciocutaneous Syndrome OMIM ID: 115150 |
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| Synonyms | CFC Syndrome; Cfcs | ||||||||||||||||||||||||||||||||||||
| 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 |
| Braftm1Bbd/Braf+ |
B6.129-Braftm1Bbd | J:170095 | View |
| Braftm1Bbd/Braf+ |
involves: 129S1/Sv * 129X1/SvJ * C57BL/6J | J:170095 | View |
| Braftm1Bbd/Braf+ |
involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * CD-1 | J:170095 | 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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