Q-omics provides the consensus-scored TRIM64C profile across patient tissues and cancer cell-line models. TRIM64C expression is associated with patient survival in 9 of 34 cancer types, with the highest sampling consensus in THCA. Additionally, TRIM64C RNA expression shows 5,682 significant gene co-expression associations, with the highest sampling consensus in UCEC. Together, these results highlight THCA, and UCEC as cancer lineages where TRIM64C 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 TRIM64C — synthetic lethality, tumor antigen, and pembrolizumab response.
This table summarizes TRIM64C survival associations across molecular data types. TRIM64C RNA expression shows survival associations in the most cancer types (9). The rightmost column indicates the cancer type with the highest sampling consensus for each molecular layer.
This table ranks reproducible TRIM64C RNA expression–survival associations across cancer types. High TRIM64C expression shows unfavorable associations in THCA, LIHC, PAAD, DLBC and MESO, but favorable associations in HNSC. The THCA 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 THCA as the clearest survival context for TRIM64C RNA expression.
This table shows molecular features associated with TRIM64C in patient tissues and cancer cell lines. In patient samples, TRIM64C shows the broadest associations at the RNA and protein expression levels, with UCEC recurring as the lineage with the largest associated feature set. In cancer cell lines, TRIM64C RNA and mutation anchors are most strongly linked to RNA-expression features, especially in LARGE_INTESTINE.
