| Human Disease |
Wiskott-Aldrich Syndrome; WAS OMIM ID: 301000 |
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| Synonyms | Aldrich Syndrome; Eczema-Thrombocytopenia-Immunodeficiency Syndrome; Immunodeficiency 2; IMD2; Wiskott-Aldrich Syndrome 1; WAS1 | ||||||||||||||||||||||||||||
| 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 |
| Wastm1Sbs/Wastm1Sbs |
129S6/SvEvTac-Wastm1Sbs/J | J:180407 | View |
| Wastm1Sbs/Wastm1Sbs |
either: (involves: 129S6/SvEvTac) or (involves: 129S6/SvEvTac * C57BL/6) | J:48836 | View |
| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Foxp3sf/Y |
involves: 101/H * C3H/HeH * STOCK MR | J:10398 | View |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc |
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last database update 06/05/2013 MGI 5.13 |
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