| Human Disease |
Achondrogenesis, Type II; ACG2 OMIM ID: 200610 |
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| Synonyms | Achondrogenesis, Langer-Saldino Type; Chondrogenesis Imperfecta | |||||||||||||||||||||
| 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/Col2a1tm1Prc |
involves: 129/Sv | J:117910 | 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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