Q-omics provides the consensus-scored EFL1P2 profile across patient tissues and cancer cell-line models. EFL1P2 expression is associated with patient survival in 15 of 34 cancer types, with the highest sampling consensus in COAD. Among the 18 cancer types available for tumor–normal comparison, EFL1P2 is differentially expressed in 5, with the highest sampling consensus in LIHC. Additionally, EFL1P2 RNA expression shows 7,423 significant gene co-expression associations, with the highest sampling consensus in COAD. Together, these results highlight COAD, and LIHC as cancer lineages where EFL1P2 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 EFL1P2 — synthetic lethality, tumor antigen, and pembrolizumab response.
This table summarizes EFL1P2 survival associations across molecular data types. EFL1P2 RNA expression shows survival associations in the most cancer types (15). The rightmost column indicates the cancer type with the highest sampling consensus for each molecular layer.
This table ranks reproducible EFL1P2 RNA expression–survival associations across cancer types. High EFL1P2 expression shows unfavorable associations in COAD, STAD, ACC, CESC and KIRC, but favorable associations in LUSC. The COAD 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 COAD as the clearest survival context for EFL1P2 RNA expression.
This table summarizes EFL1P2 tumor–normal expression differences by data type. RNA shows broader differences across cancer types, with a lineage consensus of 5. The strongest signals are observed in BRCA for RNA.
This table ranks reproducible tumor–normal expression differences for EFL1P2. A negative fold-change indicates higher expression in normal tissue than in tumor tissue. EFL1P2 shows higher tumor expression in LIHC, BRCA, LUSC, HNSC and LUAD. The LIHC box plot shows higher EFL1P2 RNA expression in tumor versus normal tissue (log2 FC = +0.043, t-test p < 0.001).
This table shows molecular features associated with EFL1P2 in patient tissues and cancer cell lines. In patient samples, EFL1P2 shows the broadest associations at the RNA and protein expression levels, with COAD recurring as the lineage with the largest associated feature set.
