| Human Disease |
Waardenburg Syndrome, Type 4b; WS4B OMIM ID: 613265 |
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| Synonyms | Waardenburg Syndrome, Type 4b, with Hirschsprung Disease; Waardenburg Syndrome, Type IVB | |||||||||||||||||||||
| 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 |
| Edn3tm1Ywa/Edn3tm1Ywa |
involves: 129S7/SvEvBrd | J:22207 | View |
| Edn3tmgc48/Edn3tmgc48 |
C57BL/6-19PWK | J:137432 | View |
| Edn3tmgc48/Edn3+ |
C57BL/6-19PWK | J:137432 | 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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