long intergenic non-protein coding RNA 2733Genealiases: []
Q-omics provides the consensus-scored LINC02733 profile across patient tissues and cancer cell-line models. LINC02733 expression is associated with patient survival in 20 of 34 cancer types, with the highest sampling consensus in SKCM. Among the 18 cancer types available for tumor–normal comparison, LINC02733 is differentially expressed in 5, with the highest sampling consensus in KICH. Additionally, LINC02733 RNA expression shows 6,523 significant pathway-activity associations, with the highest sampling consensus in STAD. Together, these results highlight SKCM, KICH, and STAD as cancer lineages where LINC02733 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 LINC02733 — synthetic lethality, tumor antigen, and pembrolizumab response.
This table summarizes LINC02733 survival associations across molecular data types. LINC02733 RNA expression shows survival associations in the most cancer types (20). The rightmost column indicates the cancer type with the highest sampling consensus for each molecular layer.
This table ranks reproducible LINC02733 RNA expression–survival associations across cancer types. High LINC02733 expression shows unfavorable associations in LUSC, COAD, CHOL, HNSC and CESC, but favorable associations in SKCM. The SKCM 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 SKCM as the clearest survival context for LINC02733 RNA expression.
This table summarizes LINC02733 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 KICH for RNA.
This table ranks reproducible tumor–normal expression differences for LINC02733. A negative fold-change indicates higher expression in normal tissue than in tumor tissue. LINC02733 shows lower tumor expression in KICH and PAAD and higher tumor expression in KIRC, KIRP and BLCA. The KICH box plot shows higher LINC02733 RNA expression in normal versus tumor tissue (log2 FC = −0.089, t-test p = .011).
This table shows molecular features associated with LINC02733 in patient tissues and cancer cell lines. In patient samples, LINC02733 shows the broadest associations at the RNA and protein expression levels, with STAD recurring as the lineage with the largest associated feature set.
