| Human Disease |
Oculopalatocerebral Syndrome OMIM ID: 257910 |
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| Synonyms | Oculopalatocerebral Dwarfism; Opc Dwarfism | |||||||||||||||||||||
| 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 |
| Cdkn2atm1Cjs/Cdkn2atm1Cjs |
involves: 129X1/SvJ * C57BL/6 | J:75215 | View |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc |
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last database update 06/12/2013 MGI 5.14 |
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