Q-omics provides the consensus-scored THRAP3P1 profile across patient tissues and cancer cell-line models. THRAP3P1 expression is associated with patient survival in 16 of 34 cancer types, with the highest sampling consensus in KICH. Among the 18 cancer types available for tumor–normal comparison, THRAP3P1 is differentially expressed in 4, with the highest sampling consensus in COAD. Additionally, THRAP3P1 RNA expression shows 9,253 significant gene co-expression associations, with the highest sampling consensus in TGCT. Together, these results highlight KICH, COAD, and TGCT as cancer lineages where THRAP3P1 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 THRAP3P1 — synthetic lethality, tumor antigen, and pembrolizumab response.
This table summarizes THRAP3P1 survival associations across molecular data types. THRAP3P1 RNA expression shows survival associations in the most cancer types (16). The rightmost column indicates the cancer type with the highest sampling consensus for each molecular layer.
This table ranks reproducible THRAP3P1 RNA expression–survival associations across cancer types. High THRAP3P1 expression shows unfavorable associations in KICH, LGG and READ, but favorable associations in BLCA, CESC and LUAD. 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 THRAP3P1 RNA expression.
This table summarizes THRAP3P1 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 THCA for RNA.
This table ranks reproducible tumor–normal expression differences for THRAP3P1. A negative fold-change indicates higher expression in normal tissue than in tumor tissue. THRAP3P1 shows lower tumor expression in THCA and READ and higher tumor expression in COAD and HNSC. The COAD box plot shows higher THRAP3P1 RNA expression in tumor versus normal tissue (log2 FC = +0.051, t-test p = .018).
This table shows molecular features associated with THRAP3P1 in patient tissues and cancer cell lines. In patient samples, THRAP3P1 shows the broadest associations at the RNA and protein expression levels, with TGCT recurring as the lineage with the largest associated feature set.
