regulator of chromosome condensation 2 pseudogene 3Genealiases: []
Q-omics provides the consensus-scored RCC2P3 profile across patient tissues and cancer cell-line models. RCC2P3 expression is associated with patient survival in 13 of 34 cancer types, with the highest sampling consensus in UCS. Among the 18 cancer types available for tumor–normal comparison, RCC2P3 is differentially expressed in 1, with the highest sampling consensus in COAD. Additionally, RCC2P3 RNA expression shows 6,217 significant pathway-activity associations, with the highest sampling consensus in STAD. Together, these results highlight UCS, COAD, and STAD as cancer lineages where RCC2P3 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 RCC2P3 — synthetic lethality, tumor antigen, and pembrolizumab response.
This table summarizes RCC2P3 survival associations across molecular data types. RCC2P3 RNA expression shows survival associations in the most cancer types (13). The rightmost column indicates the cancer type with the highest sampling consensus for each molecular layer.
This table ranks reproducible RCC2P3 RNA expression–survival associations across cancer types. High RCC2P3 expression shows unfavorable associations in UCS, BRCA, READ and ESCA, but favorable associations in BLCA and PRAD. The UCS Kaplan–Meier curve shows clear separation, with the high-expression group declining faster, consistent with the unfavorable association (log-rank p = .003). Together, the overview and detailed table identify UCS as the clearest survival context for RCC2P3 RNA expression.
This table summarizes RCC2P3 tumor–normal expression differences by data type. RNA shows broader differences across cancer types, with a lineage consensus of 1. The strongest signals are observed in COAD for RNA.
This table ranks reproducible tumor–normal expression differences for RCC2P3. A negative fold-change indicates higher expression in normal tissue than in tumor tissue. RCC2P3 shows higher tumor expression in COAD. The COAD box plot shows higher RCC2P3 RNA expression in tumor versus normal tissue (log2 FC = +0.025, t-test p = .026).
This table shows molecular features associated with RCC2P3 in patient tissues and cancer cell lines. In patient samples, RCC2P3 shows the broadest associations at the RNA and protein expression levels, with STAD recurring as the lineage with the largest associated feature set.
