| Human Disease |
Corneal Dystrophy, Posterior Polymorphous, 1; PPCD1 OMIM ID: 122000 |
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| Synonyms | Corneal Dystrophy, Hereditary Polymorphous Posterior; Posterior Polymorphous Corneal Dystrophy; PPCD | |||||||||||||||||||||
| View all models | View ALL (2) 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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Transgenes and other genome features |
Transgenes and other genome features developed in mice to model this disease.
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| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Dp(2Csrp2bp-6330439K17Rik)1Bra/0 |
D2.129-Dp(2Csrp2bp-6330439K17Rik)1Bra | J:164007 | View |
| Dp(2Csrp2bp-6330439K17Rik)1Bra/0 |
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 | J:164007 | View |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc |
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last database update 06/05/2013 MGI 5.13 |
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