Basic information of MT-ND3 :
| Official Symbol of Gene | MT-ND3 |
| Species | Homo sapiens |
| Entrez Gene ID | 4537 |
| Official Full Name | mitochondrially encoded NADH dehydrogenase 3 |
| Also known as | MTND3; ND3 |
| Gene Type | protein coding |
| dbXrefs | MIM:516002; AllianceGenome:HGNC:7458 |
| Map Location | N/A |
| Variation Type | polymorphism |
| refSNP ID | Nt 10142 C>T |
Sample information of multiple sclerosis:
| Detected Sample | peripheral blood |
| Sample Detail | N/A |
| Detected Method | PCR |
| Disease | MS |
| Disease subtype | N/A |
| Population | Filipino |
| Sample Size | 200 MS / 100 healthy subjects |
Literature information of multiple sclerosis :
| Pubmed ID | 25172194 |
| Year | 2014 |
| Title | Mitochondrial complex I gene variations; as a potential genetic risk factor in pathogenesis of multiple sclerosis |
Results of multiple sclerosis :
| Risk Type | Disease risk |
| Main Result | Positive |
| Result | Our results indicated that the prevalence of ND3 gene variations was significantly higher in patients than in healthy controls.We failed to detect Nt 10142 C>T variations in the control group. |
| Mechanism/Pathway | The mitochondria can play fundamental roles in the pathogenesis of MS.Complex I deficiency may contribute to disease susceptibility in MS. |
