| Human Disease |
Waardenburg Syndrome, Type 3; WS3 OMIM ID: 148820 |
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| Synonyms | Klein-Waardenburg Syndrome; Waardenburg Syndrome with Upper Limb Anomalies; Waardenburg Syndrome, Type III | |||||||||||||||||||||
| View all models | View ALL (5) "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 |
| Pax3Sp-d/Pax3Sp-d |
C57BL/6J | J:238 | View |
| Pax3Sp-2H/Pax3Sp-2H |
involves: 101 * C3H/He * CBA/Ca | J:46341 | View |
| Pax3Sp-2H/Pax3Sp-2H |
involves: C57BL/6 | J:14096 | View |
| Pax3Sp-d/Pax3+ |
C57BL/6J | J:238 | View |
| Pax3Sp-2H/Pax3+ |
involves: C57BL/6 | J:14096 | 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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