| Human Disease |
Immunodysregulation, Polyendocrinopathy, and Enteropathy, X-Linked; OMIM ID: 304790 |
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| Synonyms | Autoimmunity-Immunodeficiency Syndrome, X-Linked; Diabetes Mellitus, Congenital Insulin-Dependent, with Fatal Secretory Diarrhea; Diarrhea, Polyendocrinopathy, Fatal Infection Syndrome, X-Linked; Enteropathy, Autoimmune, with Hemolytic Anemia and Polyendocrinopathy; IDDM-Secretory Diarrhea Syndrome; DMSD; IPEX; Polyendocrinopathy, Immune Dysfunction, and Diarrhea, X-Linked; XPID; X-Linked Autoimmunity-Allergic Dysregulation Syndrome; XLAAD | |||||||||||||||||||||
| 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 |
| Foxp3sf/Y |
B6.Cg-Foxp3sf | J:167802 | View |
| Foxp3sf/Y |
either: 129Rl.Cg-Foxp3sf or (involves: 101/Rl * C3Hf/Rl * STOCK MR) | J:66734 | 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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