Publication for ERCC8 and NDUFAF2
| Species | Symbol | Function* | Entrez Gene ID* | Other ID | Gene coexpression |
CoexViewer |
|---|---|---|---|---|---|---|
| hsa | ERCC8 | ERCC excision repair 8, CSA ubiquitin ligase complex subunit | 1161 | [link] | ||
| hsa | NDUFAF2 | NADH:ubiquinone oxidoreductase complex assembly factor 2 | 91942 |
| Pubmed ID | Priority | Text |
|---|---|---|
| 31616255 | 0.95 | NDUFAF2, ERCC8, and ELOVL7 genes on chromosome 5 has been reported. |
| 22865506 | 0.91 | ERCC8 and a more distal heterozygous deletion within NDUFAF2. |
| 0.82 | ERCC8, a gene associated with Cockayne syndrome, and NDUFAF2, a gene associated with mitochondrial complex I deficiency. | |
| 0.81 | ERCC8 and NDUFAF2. | |
| 21680271 | 0.78 | NDUFAF2, ERCC8 and ELOVL7. |
| 23702311 | 0.51 | Ndufaf2 related pathology, the only study that examined patient-based material used fibroblasts harboring a contiguous deletion of the neighboring genes ELOVL7, ERCC8 and NDUFAF2. |
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