cytochrome c oxidase subunit 6B1 pseudogene 5Genealiases: []
Q-omics provides the consensus-scored COX6B1P5 profile across patient tissues and cancer cell-line models. COX6B1P5 expression is associated with patient survival in 24 of 34 cancer types, with the highest sampling consensus in UVM. Among the 18 cancer types available for tumor–normal comparison, COX6B1P5 is differentially expressed in 12, with the highest sampling consensus in LUAD. Additionally, COX6B1P5 RNA expression shows 15,646 significant gene co-expression associations, with the highest sampling consensus in DLBC. Together, these results highlight UVM, LUAD, and DLBC as cancer lineages where COX6B1P5 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 COX6B1P5 — synthetic lethality, tumor antigen, and pembrolizumab response.
This table summarizes COX6B1P5 survival associations across molecular data types. COX6B1P5 RNA expression shows survival associations in the most cancer types (24). The rightmost column indicates the cancer type with the highest sampling consensus for each molecular layer.
This table ranks reproducible COX6B1P5 RNA expression–survival associations across cancer types. High COX6B1P5 expression shows unfavorable associations in UVM, COAD, LGG and SARC, but favorable associations in GBM and UCS. The UVM Kaplan–Meier curve shows clear separation, with the high-expression group declining faster, consistent with the unfavorable association (log-rank p < 0.001). Together, the overview and detailed table identify UVM as the clearest survival context for COX6B1P5 RNA expression.
This table summarizes COX6B1P5 tumor–normal expression differences by data type. RNA shows broader differences across cancer types, with a lineage consensus of 12. The strongest signals are observed in LUAD for RNA.
This table ranks reproducible tumor–normal expression differences for COX6B1P5. A negative fold-change indicates higher expression in normal tissue than in tumor tissue. COX6B1P5 shows higher tumor expression in LUAD, LUSC, BLCA, KIRC, BRCA and COAD. The LUAD box plot shows higher COX6B1P5 RNA expression in tumor versus normal tissue (log2 FC = +0.543, t-test p < 0.001).
This table shows molecular features associated with COX6B1P5 in patient tissues and cancer cell lines. In patient samples, COX6B1P5 shows the broadest associations at the RNA and protein expression levels, with DLBC recurring as the lineage with the largest associated feature set.
