Q-omics provides the consensus-scored RN7SKP87 profile across patient tissues and cancer cell-line models. RN7SKP87 expression is associated with patient survival in 15 of 34 cancer types, with the highest sampling consensus in UCS. Among the 18 cancer types available for tumor–normal comparison, RN7SKP87 is differentially expressed in 7, with the highest sampling consensus in LUSC. Additionally, RN7SKP87 RNA expression shows 12,924 significant gene co-expression associations, with the highest sampling consensus in UVM. Together, these results highlight UCS, LUSC, and UVM as cancer lineages where RN7SKP87 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 RN7SKP87 — synthetic lethality, tumor antigen, and pembrolizumab response.
This table summarizes RN7SKP87 survival associations across molecular data types. RN7SKP87 RNA expression shows survival associations in the most cancer types (15). The rightmost column indicates the cancer type with the highest sampling consensus for each molecular layer.
This table ranks reproducible RN7SKP87 RNA expression–survival associations across cancer types. High RN7SKP87 expression shows unfavorable associations in CESC, STAD, ESCA and KIRP, but favorable associations in UCS and UCEC. The UCS Kaplan–Meier curve shows clear separation, with the low-expression group declining faster, consistent with the favorable association (log-rank p = .001). Together, the overview and detailed table identify UCS as the clearest survival context for RN7SKP87 RNA expression.
This table summarizes RN7SKP87 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 LUSC for RNA.
This table ranks reproducible tumor–normal expression differences for RN7SKP87. A negative fold-change indicates higher expression in normal tissue than in tumor tissue. RN7SKP87 shows lower tumor expression in THCA and higher tumor expression in LUSC, UCEC, CHOL, KIRC and KICH. The LUSC box plot shows higher RN7SKP87 RNA expression in tumor versus normal tissue (log2 FC = +0.177, t-test p = .004).
This table shows molecular features associated with RN7SKP87 in patient tissues and cancer cell lines. In patient samples, RN7SKP87 shows the broadest associations at the RNA and protein expression levels, with UVM recurring as the lineage with the largest associated feature set.
