Publication for COX7B and UQCRQ
| Species | Symbol | Function* | Entrez Gene ID* | Other ID | Gene coexpression |
CoexViewer |
|---|---|---|---|---|---|---|
| hsa | COX7B | cytochrome c oxidase subunit 7B | 1349 | [link] | ||
| hsa | UQCRQ | ubiquinol-cytochrome c reductase complex III subunit VII | 27089 |
| Pubmed ID | Priority | Text |
|---|---|---|
| 26550561 | 0.92 | UQCRQ, NDUFS2, NDUFA6, COX7B, SDHB, NDUFB7, NDUFV2, NDUFB3, NDUFC1, NDUFB6, NDUFV1, UQCRFS1, NDUFA2, NDUFS4, COX7C, NDUFA8, NDUFB9, ATP5B, ATP5C1, ATP5F1, ETFA, SLC25A4, COX7A1, IDH3B, IDH3A, PDHB, MDH2, DLD, ATP5L, and PPA2. |
| 29416685 | 0.92 | UQCRQ), 14 genes for complex IV cytochrome c oxidase (COX4I1, COX4I2, COX5A, COX5B, COX6A1, COX6A2, COX6B1, COX6B2, COX6C, COX7A2, COX7A2L, COX7B, COX8A, and COX8C), and 25 genes for complex V ATP synthase (ATP12A, ATP4A, ATP4B, ATP5A1, ATP5B, ATP5C1, ATP5F1, ATP5G1, ATP5G2, ATP5G3, ATP5H, ATP5I, ATP5J, ATP5J2, ATP5L, ATP5O, ATP6V0A2, ATP6V0D2, ATP6V1C2, ATP6V1E2, ATP6V1G3, LHPP, OXA1L, PPA1, and PPA2) (Figure 4A). |
| 29038524 | 0.72 | Cox7b, Ndufa5, Ndufb9, Ndufs7 and Uqcrq; "hydrogen ion transmembrane transport and activity" was the most significant enrichment term in biological processes category (Fig. 2b), which included 5 genes: Atp5e, Atp5o, Cox4i1, Cox7b and Uqcrq (Table S3). |
| 28545499 | 0.65 | UQCRQ, ATP5J, COX7A2, COX7B, COX6A1) and CRP or DAS28(CRP) were performed to discard a CRP or disease activity effect on the gene expression levels from this signature linked to a supposedly more pronounced mitochondrial activity in the inflammatory state. |
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