| Human Disease |
Chromosome 22q11.2 Deletion Syndrome, Distal OMIM ID: 611867 |
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| Synonyms | Distal Chromosome 22q11.2 Deletion Syndrome | ||||||
| View all models | View ALL (2) mouse models for this human disease. | ||||||
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Genes and mouse models |
There are currently no human or mouse genes associated with this disease in the MGI database. | ||||||
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Transgenes and other genome features |
Transgenes and other genome features developed in mice to model this disease.
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| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Del(16Es2el-Ufd1l)217Bld/+ |
B6.129S7-Del(16Es2el-Ufd1l)217Bld | J:190908 | View |
| Del(16Es2el-Ufd1l)217Bld/+ |
involves: 129S7/SvEvBrd * C57BL/6 | J:57757 | 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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