Q-omics provides the consensus-scored RN7SKP68 profile across patient tissues and cancer cell-line models. RN7SKP68 expression is associated with patient survival in 12 of 34 cancer types, with the highest sampling consensus in ACC. Among the 18 cancer types available for tumor–normal comparison, RN7SKP68 is differentially expressed in 7, with the highest sampling consensus in KICH. Additionally, RN7SKP68 RNA expression shows 10,561 significant gene co-expression associations, with the highest sampling consensus in THYM. Together, these results highlight ACC, KICH, and THYM as cancer lineages where RN7SKP68 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 RN7SKP68 — synthetic lethality, tumor antigen, and pembrolizumab response.
This table summarizes RN7SKP68 survival associations across molecular data types. RN7SKP68 RNA expression shows survival associations in the most cancer types (12). The rightmost column indicates the cancer type with the highest sampling consensus for each molecular layer.
This table ranks reproducible RN7SKP68 RNA expression–survival associations across cancer types. High RN7SKP68 expression shows unfavorable associations in ACC, OV, COAD and STAD, but favorable associations in KIRC and TGCT. The ACC 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 ACC as the clearest survival context for RN7SKP68 RNA expression.
This table summarizes RN7SKP68 tumor–normal expression differences by data type. RNA shows broader differences across cancer types, with a lineage consensus of 7. The strongest signals are observed in KICH for RNA.
This table ranks reproducible tumor–normal expression differences for RN7SKP68. A negative fold-change indicates higher expression in normal tissue than in tumor tissue. RN7SKP68 shows lower tumor expression in KICH, KIRP, LUAD and LUSC and higher tumor expression in BLCA and HNSC. The KICH box plot shows higher RN7SKP68 RNA expression in normal versus tumor tissue (log2 FC = −0.506, t-test p < 0.001).
This table shows molecular features associated with RN7SKP68 in patient tissues and cancer cell lines. In patient samples, RN7SKP68 shows the broadest associations at the RNA and protein expression levels, with THYM recurring as the lineage with the largest associated feature set.
