COX20, cytochrome c oxidase assembly factor COX20

COX20, cytochrome c oxidase assembly factor COX20

• This gene encodes a protein that plays a role in the assembly of cytochrome C oxidase, an important component of the respiratory pathway. It contains two transmembrane helices and localizes to the mitochondrial membrane. Mutations in this gene can cause mitochondrial complex IV deficiency, which results in ataxia and muscle hypotonia. There are multiple pseudogenes for this gene. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2015]

• Gene Synonyms (FAM36A, cytochrome c oxidase assembly protein COX20, mitochondrial, COX20 Cox2 chaperone homolog, COX20, cytochrome c oxidase assembly factor, cytochrome c oxidase protein 20 homolog, family with sequence similarity 36, member A,)
• NCBI Gene ID: 116228
• Species: Homo sapiens (Human)
• UNIPROT ID#>>B3KM21
  UNIPROT ID#>>Q5RI15
• View the NCBI Database for this Gene »

Gene products are often involved in multiple pathways and networks within a living cell. Learn more about other interacting partners.

cytochrome c oxidase assembly factor COX20 interacts with:

• chromosome 16 open reading frame 91
  golgi transport 1A
  NCBP2 antisense 2 (head to head)
  solute carrier family 10 member 6
  testis expressed 44
  transmembrane protein 31

Paste a protein or nucleic acid sequence in the box below to confirm that it matches this gene’s reference sequence(s). Click on a link under RELATED ORF CLONES to see how a sequence matches to an experimentally-validated ORF clone.