| Human Disease |
Microphthalmia, Isolated 6; MCOP6 OMIM ID: 613517 |
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| Synonyms | Microphthalmia, Posterior Nonsyndromic | |||||||||||||||||||||
| View all models | View ALL (3) 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 |
| Prss56glcr4/Prss56glcr4 |
C3A.Cg-Prss56glcr4 Pde6b+ | J:188765 | View |
| Prss56glcr4/Prss56glcr4 |
C57BL/6J-Prss56glcr4 | J:188765 | View |
| Prss56glcr4/Prss56glcr4 |
involves: C3H/HeA * C57BL/6J * C57BL/LiA | J:188765 | 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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