| Human Disease |
Coffin-Lowry Syndrome; CLS OMIM ID: 303600 |
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| 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 |
| Rps6ka3tm1.1Kry/Rps6ka3tm1.1Kry |
involves: 129X1/SvJ | J:89403 | View |
| Rps6ka3tm1.1Kry/Rps6ka3+ |
involves: 129X1/SvJ | J:89403 | View |
| Rps6ka3tm1Ljg/Y |
involves: 129 * C57BL/6 | J:67575, J:83536 | 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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