?mitochondrial complex iv deficiency Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description OMIM mapping confirmed by DO. [SN]. (Human Disease Ontology, DOID_3762)
External Link http://www.omim.org/entry/220110
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4 genes associated with the ?mitochondrial complex iv deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
COX14 COX14 cytochrome c oxidase assembly factor
COX6B1 cytochrome c oxidase subunit VIb polypeptide 1 (ubiquitous)
FASTKD2 FAST kinase domains 2
TACO1 translational activator of mitochondrially encoded cytochrome c oxidase I