| Human Disease |
Chromosome 10q23 Deletion Syndrome OMIM ID: 612242 |
||||||
| View all models | View ALL (1) mouse models for this human disease. | ||||||
|
Genes and mouse models |
There are currently no human or mouse genes associated with this disease in the MGI database. | ||||||
|
Transgenes and other genome features |
Transgenes and other genome features developed in mice to model this disease.
|
| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Tg(CAG-Bmpr1a*,-lacZ)1Nobs/0 Tg(Mpz-cre)94Imeg/0 |
involves: 129X1/SvJ * C57BL/6J | J:192670 | View |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc |
||
|
Citing These Resources Funding Information Warranty Disclaimer & Copyright Notice Send questions and comments to User Support. |
last database update 05/08/2013 MGI 5.13 |
|
|
|
||