| Human Disease |
Corneal Dystrophy, Fuchs Endothelial, 1; FECD1 OMIM ID: 136800 |
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| Synonyms | Corneal Dystrophy, Fuchs Endothelial, Early-Onset | |||||||||||||||||||||
| View all models | View ALL (1) mouse models for this human disease. | |||||||||||||||||||||
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Genes and mouse models |
Mutations in human and/or mouse homologs are associated with this disease
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| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Col8a2tm1.1Asj/Col8a2tm1.1Asj |
involves: C57BL/6 * CBA | J:179022 | View |
| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Col8a2Aca23/Col8a2Aca23 |
C57BL/6J-Col8a2Aca23 | J:158259 | View |
| Col8a1tm1Bjro/Col8a1tm1Bjro Col8a2tm1Bjro/Col8a2tm1Bjro |
B6.129S4-Col8a2tm1Bjro Col8a1tm1Bjro | J:100136 | View |
| Col8a2Aca23/Col8a2+ |
C57BL/6J-Col8a2Aca23 | J:158259 | 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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