Cytochrome c oxidase assembly factor COX20 is a protein that in humans is encoded by the COX20 gene. This gene encodes a protein that plays a role in the assembly of cytochrome c oxidase, an important component of the respiratory pathway. Mutations in this gene can cause mitochondrial complex IV deficiency. There are multiple pseudogenes for this gene. Alternative splicing results in multiple transcript variants.[1]
^
"Entrez Gene: Cytochrome c oxidase assembly factor COX20". Retrieved 2018-08-08. This article incorporates text from this source, which is in the public domain.
Cytochrome c oxidase assembly factor COX20 is a protein that in humans is encoded by the COX20 gene. This gene encodes a protein that plays a role in...
identified in seven COX assembly factors: SURF1, SCO1, SCO2, COX10, COX15, COX20, COA5 and LRPPRC. Mutations in these proteins can result in altered functionality...
prevents its premature turnover. Additionally, it interacts with TMEM177 in a COX20-dependent manner. GRCh38: Ensembl release 89: ENSG00000198804 – Ensembl...
interacts with COA6, TMEM177, COX20, COX16, COX17, WDR19, CIDEB, and UBC7. It is also found in a complex with TMEM177, COX20, COA6, MT-CO2/COX2, COX18, and...
composed of 125 amino acids. The COA6 protein is found a complex with TMEM177, COX20, MT-CO2/COX2, COX18, SCO1 and SCO2. The protein has a CX9CXnCX10C motif...
interactions, SCO2 has been found to interact with COA6, THEM177 in a COX20-dependent manner, COX20, COX16, SCO1, and others. GRCh38: Ensembl release 89: ENSG00000284194...
Global Information
This article incorporates text from this source, which is in the public domain.
