cytochrome c oxidase subunit IGenealiases: COI · MTCO1
Q-omics provides the consensus-scored MT-CO1 profile across patient tissues and cancer cell-line models. MT-CO1 expression is associated with patient survival in 23 of 34 cancer types, with the highest sampling consensus in ACC. Among the 18 cancer types available for tumor–normal comparison, MT-CO1 is differentially expressed in 12, with the highest sampling consensus in KIRC. Additionally, MT-CO1 RNA expression shows 18,877 significant gene co-expression associations, with the highest sampling consensus in ACC. Together, these results highlight ACC, and KIRC as cancer lineages where MT-CO1 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 MT-CO1 — synthetic lethality, tumor antigen, and pembrolizumab response.
This table summarizes MT-CO1 survival associations across molecular data types. MT-CO1 RNA expression shows survival associations in the most cancer types (23), followed by mass-spec protein abundance (5). The rightmost column indicates the cancer type with the highest sampling consensus for each molecular layer.
This table ranks reproducible MT-CO1 RNA expression–survival associations across cancer types. High MT-CO1 expression shows favorable associations in ACC, LGG, KICH, KIRC, PAAD and LIHC. The ACC 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 ACC as the clearest survival context for MT-CO1 RNA expression.
This table summarizes MT-CO1 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 6. The strongest signals are observed in KIRC for RNA and CCRCC for protein.
This table ranks reproducible tumor–normal expression differences for MT-CO1. A negative fold-change indicates higher expression in normal tissue than in tumor tissue. MT-CO1 shows lower tumor expression in KIRC, HNSC, COAD, KIRP and LUSC and higher tumor expression in KICH. The KIRC box plot shows higher MT-CO1 RNA expression in normal versus tumor tissue (log2 FC = −0.791, t-test p < 0.001).
This table shows molecular features associated with MT-CO1 in patient tissues and cancer cell lines. In patient samples, MT-CO1 shows the broadest associations at the RNA and protein expression levels, with ACC recurring as the lineage with the largest associated feature set. In cancer cell lines, MT-CO1 RNA and mutation anchors are most strongly linked to RNA-expression features, especially in UPPER_AERODIGESTIVE_TRACT, while CRISPR and shRNA rows add functional-dependency signals in LUNG_NSCLC_LUAD and BREAST.
