| Human Disease |
Incontinentia Pigmenti; IP OMIM ID: 308300 |
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| Synonyms | Bloch-Sulzberger Syndrome; Incontinentia Pigmenti, Familial Male-Lethal Type; Incontinentia Pigmenti, Type II, Formerly; IP2, FORMERLY | |||||||||||||||||||||
| 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 |
| Ikbkgtm1Mka/Ikbkg+ |
involves: 129S1/Sv * 129X1/SvJ * C57BL/6J | J:63054 | View |
| Ikbkgtm1Mpa/Ikbkg+ |
involves: C57BL/6 | J:63055 | 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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