| Human Disease |
Pierson Syndrome OMIM ID: 609049 |
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| Synonyms | Microcoria-Congenital Nephrotic Syndrome | ||||||||||||||||||||||||||||
| View all models | View ALL (2) 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 |
| Lamb2tm1Jrs/Lamb2tm1Jrs |
involves: 129S1/Sv * 129X1/SvJ | J:106005 | View |
| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Tenc1nph/Tenc1nph |
involves: ICR | J:108691 | 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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