Q-omics provides the consensus-scored RAD1P1 profile across patient tissues and cancer cell-line models. RAD1P1 expression is associated with patient survival in 20 of 34 cancer types, with the highest sampling consensus in KICH. Among the 18 cancer types available for tumor–normal comparison, RAD1P1 is differentially expressed in 4, with the highest sampling consensus in KIRP. Additionally, RAD1P1 RNA expression shows 8,166 significant gene co-expression associations, with the highest sampling consensus in TGCT. Together, these results highlight KICH, KIRP, and TGCT as cancer lineages where RAD1P1 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 RAD1P1 — synthetic lethality, tumor antigen, and pembrolizumab response.
This table summarizes RAD1P1 survival associations across molecular data types. RAD1P1 RNA expression shows survival associations in the most cancer types (20). The rightmost column indicates the cancer type with the highest sampling consensus for each molecular layer.
This table ranks reproducible RAD1P1 RNA expression–survival associations across cancer types. High RAD1P1 expression shows unfavorable associations in KICH, UCEC, LIHC, ACC and CHOL, but favorable associations in LUSC. The KICH 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 KICH as the clearest survival context for RAD1P1 RNA expression.
This table summarizes RAD1P1 tumor–normal expression differences by data type. RNA shows broader differences across cancer types, with a lineage consensus of 4. The strongest signals are observed in KIRP for RNA.
This table ranks reproducible tumor–normal expression differences for RAD1P1. A negative fold-change indicates higher expression in normal tissue than in tumor tissue. RAD1P1 shows lower tumor expression in KIRP and KICH and higher tumor expression in COAD and STAD. The KIRP box plot shows higher RAD1P1 RNA expression in normal versus tumor tissue (log2 FC = −0.086, t-test p = .029).
This table shows molecular features associated with RAD1P1 in patient tissues and cancer cell lines. In patient samples, RAD1P1 shows the broadest associations at the RNA and protein expression levels, with TGCT recurring as the lineage with the largest associated feature set.
