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COA5

cytochrome c oxidase assembly factor 5

HCNC Approved Symbol
COA5 (HGNC:33848)
Genomic Coordinates
2:98,599,314 - 98,608,512 (2q11.2)
Synonyms
MGC52110, FLJ27524, Pet191, C2orf64
Disease Associations
This gene is associated with the following 1 diseases in OMIM.
View More Disease Info
Disease NameOMIM IDInheritance
?Mitochondrial complex IV, deficiency, nuclear type 9
616500AR

Diagnosed Cases

0Patient

There are no patients diagnosed with a variant in the COA5 gene.

Frequently observed phenotypes

(Top 5 only, Patient count*)
*% of total patients presenting each phenotype is shown in parentheses.

No Results