Home Details
| Official Symbol of Gene | MT-CO2 |
| Species | Homo sapiens |
| Entrez Gene ID | 4513 |
| Official Full Name | mitochondrially encoded cytochrome c oxidase II |
| Also known as | COII; MTCO2; COX2 |
| Gene Type | protein coding |
| dbXrefs | MIM:516040; AllianceGenome:HGNC:7421 |
| Map Location | N/A |
| Detected Sample | PBMC |
| Sample Detail | N/A |
| Detected Method | RT-PCR |
| Disease | MS |
| Disease subtype | N/A |
| Population | N/A |
| Sample Size | 30 MS patients / 30 healthy subjects |
| Pubmed ID | 23901189 |
| Year | 2013 |
| Title | Investigation of cytocrom c oxidase gene subunits expression on the Multiple sclerosis |
| Expression | No significance |
| Risk type | Disease risk |
| Result | The results showed that there are not meaning differences in COX2 gene. |
| Mechanism/Pathway | The final respiratory chain complex (complex IV or cytochrome c oxidase [COX]) is the site at which over 90% of oxygen is consumed.There is a common symptom of MS with mitochondrial diseases such as (AD), (PD) and also the point mutation mtDNA can cause damage to the myelin. |

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