| Human Disease |
Lipodystrophy, Familial Partial, Type 2; FPLD2 OMIM ID: 151660 |
||||||||||||||||||||||||||||
| Synonyms | FPL2; Lipoatrophic Diabetes; Lipodystrophy, Familial Partial, Dunnigan Type; Lipodystrophy, Familial, of Limbs and Lower Trunk; Lipodystrophy, Reverse Partial | ||||||||||||||||||||||||||||
| 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
|
||||||||||||||||||||||||||||
|
Transgenes and other genome features |
Transgenes and other genome features developed in mice to model this disease.
|
||||||||||||||||||||||||||||
| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Zmpste24tm1Lotn/Zmpste24tm1Lotn |
involves: 129P2/Ola * C57BL/6 | J:76209 | View |
| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Lmnatm1Stw/Lmnatm1Stw |
involves: 129S1/Sv * C57BL/6J | J:75101 | View |
| Lmnatm1Stw/Lmna+ |
involves: 129S1/Sv * C57BL/6J | J:75101 | View |
| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Tg(Fabp4-LMNA*R482Q)11ACdl/0 |
FVB-Tg(Fabp4-LMNA*R482Q)11ACdl | J:149858 | View |
| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Tg(Fabp4-LMNA*R482Q)17CCdl/0 |
FVB/N-Tg(Fabp4-LMNA*R482Q)17CCdl | J:149858 | 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 06/05/2013 MGI 5.13 |
|
|
|
||