Q-omics provides the consensus-scored TRAPPC2LP1 profile across patient tissues and cancer cell-line models. TRAPPC2LP1 expression is associated with patient survival in 12 of 34 cancer types, with the highest sampling consensus in ACC. Among the 18 cancer types available for tumor–normal comparison, TRAPPC2LP1 is differentially expressed in 6, with the highest sampling consensus in COAD. Additionally, TRAPPC2LP1 RNA expression shows 14,260 significant protein co-abundance associations, with the highest sampling consensus in GBM. Together, these results highlight ACC, COAD, and GBM as cancer lineages where TRAPPC2LP1 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 TRAPPC2LP1 — synthetic lethality, tumor antigen, and pembrolizumab response.
This table summarizes TRAPPC2LP1 survival associations across molecular data types. TRAPPC2LP1 RNA expression shows survival associations in the most cancer types (12). The rightmost column indicates the cancer type with the highest sampling consensus for each molecular layer.
This table ranks reproducible TRAPPC2LP1 RNA expression–survival associations across cancer types. High TRAPPC2LP1 expression shows unfavorable associations in ACC, COAD, KICH, OV, BLCA and ESCA. The ACC 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 ACC as the clearest survival context for TRAPPC2LP1 RNA expression.
This table summarizes TRAPPC2LP1 tumor–normal expression differences by data type. RNA shows broader differences across cancer types, with a lineage consensus of 6. The strongest signals are observed in COAD for RNA.
This table ranks reproducible tumor–normal expression differences for TRAPPC2LP1. A negative fold-change indicates higher expression in normal tissue than in tumor tissue. TRAPPC2LP1 shows higher tumor expression in COAD, STAD, HNSC, LUSC, LUAD and BRCA. The COAD box plot shows higher TRAPPC2LP1 RNA expression in tumor versus normal tissue (log2 FC = +0.081, t-test p = .004).
This table shows molecular features associated with TRAPPC2LP1 in patient tissues and cancer cell lines. In patient samples, TRAPPC2LP1 shows the broadest associations at the RNA and protein expression levels, with GBM recurring as the lineage with the largest associated feature set.
