| Human Disease |
T-Cell Immunodeficiency, Congenital Alopecia, and Nail Dystrophy OMIM ID: 601705 |
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| 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 |
| Foxn1nu-Y/Foxn1nu-Y |
101/HY-Foxn1nu-Y | J:29022 | View |
| Foxn1tm1Tbo/Foxn1tm1Tbo |
involves: 129S1/Sv | J:33796 | View |
| Foxn1nu/Foxn1nu |
Not Specified | J:11959 | View |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc |
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last database update 05/22/2013 MGI 5.13 |
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