| Human Disease |
Osteopetrosis, Autosomal Recessive 4; OPTB4 OMIM ID: 611490 |
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| Synonyms | Osteopetrosis, Infantile Malignant 2 | |||||||||||||||||||||
| 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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| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Clcn7tm1Tjj/Clcn7tm1Tjj |
involves: 129P2/OlaHsd * C57BL/6 | J:67273 | View |
| Clcn7tm2Tjj/Clcn7tm2Tjj |
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 | J:67273 | View |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc |
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last database update 06/12/2013 MGI 5.14 |
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