| Human Disease |
Raine Syndrome; RNS OMIM ID: 259775 |
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| Synonyms | Osteosclerotic Bone Dysplasia, Lethal | |||||||||||||||||||||
| View all models | View ALL (1) "NOT" mouse models for this human disease. No mouse models with similarity to the expected human disease phenotype are reported in MGI. | |||||||||||||||||||||
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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 |
| Fam20ctm1.1Cqi/Fam20ctm1.1Cqi Tg(Sox2-cre)1Amc/0 |
involves: 129S6/SvEvTac * C57BL/6 * CBA | J:185208 | View |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc |
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last database update 06/05/2013 MGI 5.13 |
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