Q-omics provides the consensus-scored COQ7 profile across patient tissues and cancer cell-line models. COQ7 expression is associated with patient survival in 20 of 34 cancer types, with the highest sampling consensus in KIRC. Among the 18 cancer types available for tumor–normal comparison, COQ7 is differentially expressed in 12, with the highest sampling consensus in THCA. Additionally, COQ7 RNA expression shows 19,959 significant gene co-expression associations, with the highest sampling consensus in UVM. Together, these results highlight KIRC, THCA, and UVM as cancer lineages where COQ7 shows reproducible signals across survival, tumor–normal expression, and patient cross-omics analyses.
Every result is evaluated using two consensus scores. Sampling consensus measures how consistently a finding is reproduced within a cancer lineage across different conditions. Lineage consensus measures how broadly the result is shared across cancer types, distinguishing pan-cancer signals from lineage-specific patterns.
Premium analyses for COQ7 — synthetic lethality, tumor antigen, and pembrolizumab response.
This table summarizes COQ7 survival associations across molecular data types. COQ7 RNA expression shows survival associations in the most cancer types (20), followed by mutation status (1) and mass-spec protein abundance (6). The rightmost column indicates the cancer type with the highest sampling consensus for each molecular layer.
This table ranks reproducible COQ7 RNA expression–survival associations across cancer types. High COQ7 expression shows unfavorable associations in UVM, but favorable associations in KIRC, MESO, READ, BRCA and CESC. The KIRC Kaplan–Meier curve shows clear separation, with the low-expression group declining faster, consistent with the favorable association (log-rank p < 0.001). Together, the overview and detailed table identify KIRC as the clearest survival context for COQ7 RNA expression.
This table summarizes COQ7 tumor–normal expression differences by data type. RNA shows broader differences across cancer types, with a lineage consensus of 12, while mass-spec protein shows differences in 5. The strongest signals are observed in THCA for RNA and CCRCC for protein.
This table ranks reproducible tumor–normal expression differences for COQ7. A negative fold-change indicates higher expression in normal tissue than in tumor tissue. COQ7 shows lower tumor expression in THCA, UCEC and LUAD and higher tumor expression in LIHC, CHOL and BRCA. The THCA box plot shows higher COQ7 RNA expression in normal versus tumor tissue (log2 FC = −0.989, t-test p < 0.001).
This table shows molecular features associated with COQ7 in patient tissues and cancer cell lines. In patient samples, COQ7 shows the broadest associations at the RNA and protein expression levels, with UVM recurring as the lineage with the largest associated feature set. In cancer cell lines, COQ7 RNA and mutation anchors are most strongly linked to RNA-expression features, especially in LIVER, while CRISPR and shRNA rows add functional-dependency signals in SKIN and BLOOD_Leukemia.
