| Human Disease |
Wilms Tumor, Aniridia, Genitourinary Anomalies, and Mental Retardation Syndrome; WAGR OMIM ID: 194072 |
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| Synonyms | Chromosome 11p13 Deletion Syndrome; Wagr Syndrome | |||||||||||||||||||||||||
| 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 |
| Pax6Sey-Dey/Pax6+ |
C3H/HeJ-Pax6Sey-Dey | J:10820 | 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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