| Human Disease |
Osteopetrosis, Autosomal Recessive 1; OPTB1 OMIM ID: 259700 |
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| Synonyms | Albers-Schonberg Disease, Autosomal Recessive; Marble Bones, Autosomal Recessive; Osteopetrosis, Infantile Malignant 1 | |||||||||||||||||||||
| 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 |
| Tcirg1oc/Tcirg1oc |
B6C3Fe a/a-Tcirg1oc/J | J:61295 | View |
| Tcirg1tm1Ypl/Tcirg1tm1Ypl |
involves: 129S4/SvJae * C57BL/6J | J:58795 | 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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