Q-omics provides the consensus-scored RAB11A profile across patient tissues and cancer cell-line models. RAB11A expression is associated with patient survival in 23 of 34 cancer types, with the highest sampling consensus in KIRC. Among the 18 cancer types available for tumor–normal comparison, RAB11A is differentially expressed in 11, with the highest sampling consensus in LIHC. Additionally, RAB11A RNA expression shows 19,392 significant gene co-expression associations, with the highest sampling consensus in UVM. Together, these results highlight KIRC, LIHC, and UVM as cancer lineages where RAB11A 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 RAB11A — synthetic lethality, tumor antigen, and pembrolizumab response.
This table summarizes RAB11A survival associations across molecular data types. RAB11A RNA expression shows survival associations in the most cancer types (23), followed by mutation status (5) and mass-spec protein abundance (4). The rightmost column indicates the cancer type with the highest sampling consensus for each molecular layer.
This table ranks reproducible RAB11A RNA expression–survival associations across cancer types. High RAB11A expression shows unfavorable associations in UVM, PAAD, HNSC and LIHC, but favorable associations in KIRC and UCEC. The KIRC Kaplan–Meier curve shows clear separation, with the low-expression group declining faster, consistent with the favorable association (log-rank p < 0.001). Together, the overview and detailed table identify KIRC as the clearest survival context for RAB11A RNA expression.
This table summarizes RAB11A tumor–normal expression differences by data type. RNA shows broader differences across cancer types, with a lineage consensus of 11, while mass-spec protein shows differences in 4. The strongest signals are observed in LIHC for RNA and COAD for protein.
This table ranks reproducible tumor–normal expression differences for RAB11A. A negative fold-change indicates higher expression in normal tissue than in tumor tissue. RAB11A shows lower tumor expression in LUAD and HNSC and higher tumor expression in LIHC, BRCA, CHOL and BLCA. The LIHC box plot shows higher RAB11A RNA expression in tumor versus normal tissue (log2 FC = +0.907, t-test p < 0.001).
This table shows molecular features associated with RAB11A in patient tissues and cancer cell lines. In patient samples, RAB11A shows the broadest associations at the RNA and protein expression levels, with UVM recurring as the lineage with the largest associated feature set. In cancer cell lines, RAB11A RNA and mutation anchors are most strongly linked to RNA-expression features, especially in BREAST, while CRISPR and shRNA rows add functional-dependency signals in BLOOD_Leukemia and LARGE_INTESTINE.
