| Human Disease |
Ichthyosis, X-Linked; XLI OMIM ID: 308100 |
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| Synonyms | Placental Steroid Sulfatase Deficiency; Steroid Sulfatase Deficiency; Sts Deficiency | |||||||||||||||||||||
| View all models | View ALL (2) "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 |
| Foxp3sf/Y |
involves: STOCK MR | J:14076 | 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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