| Human Disease |
Stickler Syndrome, Type I, Nonsyndromic Ocular OMIM ID: 609508 |
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| Synonyms | Stickler Syndrome, Type I, Predominantly Ocular | |||||||||||||||||||||
| 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 |
| Col2a1tm1Prc/Col2a1+ |
involves: 129/Sv * C57BL/6 | J:144313 | 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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