| Human Disease |
Cerebral Amyloid Angiopathy, Itm2b-Related, 2 OMIM ID: 117300 |
|||||||||||||||||||||
| Synonyms | Cerebellar Ataxia, Cataract, Deafness, and Dementia or Psychosis; Dementia, Familial Danish; FDD; Familial Danish Dementia; Heredopathia Ophthalmootoencephalica; HOOE | |||||||||||||||||||||
| View all models | View ALL (4) 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 |
| Itm2btm2.1Ldad/Itm2b+ |
B6.129-Itm2btm2.1Ldad | J:167154 | View |
| Itm2btm1.1Ldad/Itm2b+ |
B6.129-Itm2btm1.1Ldad | J:167154 | View |
| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Itm2btm2.1Ldad/Itm2btm2.1Ldad |
B6.129-Itm2btm2.1Ldad | J:155411 | View |
| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Tg(Prnp-ITM2B*)1Ruvi/? |
B6.C3Fe-Tg(Prnp-ITM2B*)1Ruvi | J:155720 | View |
| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Tg(Prnp-ITM2B*)7Jckr/0 |
C57BL/6-Tg(Prnp-ITM2B*)7Jckr | J:159279 | 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 |
|
|
|
||