| Human Disease |
Leber Congenital Amaurosis 4; LCA4 OMIM ID: 604393 |
|||||||||||||||||||||
| View all models | View ALL (3) mouse models for this human disease. | |||||||||||||||||||||
|
Genes and mouse models |
Mutations in human and/or mouse homologs are associated with this disease
|
|||||||||||||||||||||
| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Aipl1tm1Tili/Aipl1tm1Tili |
involves: 129S4/SvJae * C57BL/6 | J:92601 | View |
| Aipl1tm1Visu/Aipl1tm1Visu |
involves: 129S1/Sv * 129X1/SvJ * C57BL/6J | J:92617 | View |
| Aipl1tm1Mad/Aipl1tm1Mad |
involves: 129S7/SvEvBrd | J:94655 | 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 |
|
|
|
||