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Human Disease and Mouse Model Detail
Human Disease 3-methylglutaconic Aciduria, Type III; MGCA3
OMIM ID: 258501
Synonyms Costeff Syndrome; Iraqi-Jewish 'optic Atrophy Plus'; Mga, Type III; MGA3; Opa3, Autosomal Recessive; Optic Atrophy 3, Autosomal Recessive; Optic Atrophy Plus Syndrome; Optic Atrophy, Infantile, with Chorea and Spastic Paraplegia
View all models View ALL (1) mouse models for this human disease.
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* View 1 model 1:1 Homology
Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
Citing These Resources
Funding Information
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Send questions and comments to User Support. 		last database update
05/08/2013
MGI 5.13 		The Jackson Laboratory