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Human Disease and Mouse Model Detail
Human Disease Combined Oxidative Phosphorylation Deficiency 11; COXPD11
OMIM ID: 614922
Synonyms Combined Oxidative Phosphorylation Deficiency; Encephaloneuromyopathy, Infantile, Due to Mitochondrial Translation Defect
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
     Rmnd1 RMND1*   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
08/19/2014
MGI 5.19
The Jackson Laboratory