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Human Disease and Mouse Model Detail
Human Disease Osteopetrosis, Autosomal Dominant 2; OPTA2
OMIM ID: 166600
Synonyms Albers-Schonberg Disease, Autosomal Dominant; Marble Bones, Autosomal Dominant; Osteopetrosis; Osteopetrosis, Autosomal Dominant, Type II; Osteosclerosis Fragilis Generalisata
Genes and
mouse models
Mutations in human and/or mouse homologs are associated with this disease

      *Gene is associated with the disease in this species
      Mouse Homologs Human Homologs Mouse Models Mouse : Human
Homology Class
     Clcn7 CLCN7*   1:1 Homology

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
04/08/2014
MGI 5.17
The Jackson Laboratory