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Human Disease and Mouse Model Detail
Human Disease Optic Atrophy 3, Autosomal Dominant
OMIM ID: 165300
Synonyms Opa3, Autosomal Dominant; Optic Atrophy; Optic Atrophy and Cataract, Autosomal Dominant
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
     Opa3 OPA3*   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
08/26/2014
MGI 5.19
The Jackson Laboratory