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Human Disease and Mouse Model Detail
Human Disease Mitochondrial DNA Depletion Syndrome 5 (encephalomyopathic with or without Methylmalonic Aciduria); MTDPS5
OMIM ID: 612073
Human Phenotype Ontology associations
Synonyms Mitochondrial DNA Depletion Syndrome; Mitochondrial DNA Depletion Syndrome, Encephalomyopathic Form, with or without Methylmalonic Aciduria, Autosomal Recessive, Sucla2-Related
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

      *Disease is associated/modeled with this Gene or a homolog. More...
      Human Homologs Mouse Homologs Mouse Models Homology Source
     SUCLA2* Sucla2* View 1 model HomoloGene and HGNC
References Disease References using Mouse Models (1)

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
MGI 6.07
The Jackson Laboratory