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Human Disease and Mouse Model Detail
Human Disease Mitochondrial Complex IV Deficiency
OMIM ID: 220110
Human Phenotype Ontology associations
Synonyms COX Deficiency; Cytochrome C Oxidase Deficiency; Mitochondrial Complex Deficiency
View all models View ALL (3) 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
     COX10* Cox10* View 1 model HomoloGene and HGNC
SCO1* Sco1* View 1 model HomoloGene and HGNC
     SCO2 Sco2* View 1 model HomoloGene and HGNC
     APOPT1* Apopt1   HomoloGene and HGNC
COA5* Coa5   HomoloGene and HGNC
COX6B1* Cox6b1   HomoloGene and HGNC
COX14* Cox14   HomoloGene and HGNC
COX20* Cox20   HomoloGene and HGNC
FASTKD2* Fastkd2   HomoloGene and HGNC
PET100* Pet100   HomoloGene and HGNC
TACO1* Taco1   HomoloGene and HGNC
References Disease References using Mouse Models (3)

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