Q-omics provides the consensus-scored RN7SKP97 profile across patient tissues and cancer cell-line models. RN7SKP97 expression is associated with patient survival in 19 of 34 cancer types, with the highest sampling consensus in KIRC. Among the 18 cancer types available for tumor–normal comparison, RN7SKP97 is differentially expressed in 13, with the highest sampling consensus in COAD. Additionally, RN7SKP97 RNA expression shows 15,598 significant gene co-expression associations, with the highest sampling consensus in UVM. Together, these results highlight KIRC, COAD, and UVM as cancer lineages where RN7SKP97 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 RN7SKP97 — synthetic lethality, tumor antigen, and pembrolizumab response.
This table summarizes RN7SKP97 survival associations across molecular data types. RN7SKP97 RNA expression shows survival associations in the most cancer types (19). The rightmost column indicates the cancer type with the highest sampling consensus for each molecular layer.
This table ranks reproducible RN7SKP97 RNA expression–survival associations across cancer types. High RN7SKP97 expression shows unfavorable associations in KIRC, UVM, KIRP, UCEC, LIHC and ESCA. The KIRC 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 KIRC as the clearest survival context for RN7SKP97 RNA expression.
This table summarizes RN7SKP97 tumor–normal expression differences by data type. RNA shows broader differences across cancer types, with a lineage consensus of 13. The strongest signals are observed in COAD for RNA.
This table ranks reproducible tumor–normal expression differences for RN7SKP97. A negative fold-change indicates higher expression in normal tissue than in tumor tissue. RN7SKP97 shows higher tumor expression in COAD, LUAD, HNSC, KIRC, KIRP and STAD. The COAD box plot shows higher RN7SKP97 RNA expression in tumor versus normal tissue (log2 FC = +0.592, t-test p < 0.001).
This table shows molecular features associated with RN7SKP97 in patient tissues and cancer cell lines. In patient samples, RN7SKP97 shows the broadest associations at the RNA and protein expression levels, with UVM recurring as the lineage with the largest associated feature set.
