long intergenic non-protein coding RNA 555Genealiases: []
Q-omics provides the consensus-scored LINC00555 profile across patient tissues and cancer cell-line models. LINC00555 expression is associated with patient survival in 13 of 34 cancer types, with the highest sampling consensus in UCEC. Among the 18 cancer types available for tumor–normal comparison, LINC00555 is differentially expressed in 5, with the highest sampling consensus in KIRC. Additionally, LINC00555 RNA expression shows 5,809 significant pathway-activity associations, with the highest sampling consensus in STAD. Together, these results highlight UCEC, KIRC, and STAD as cancer lineages where LINC00555 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 LINC00555 — synthetic lethality, tumor antigen, and pembrolizumab response.
This table summarizes LINC00555 survival associations across molecular data types. LINC00555 RNA expression shows survival associations in the most cancer types (13). The rightmost column indicates the cancer type with the highest sampling consensus for each molecular layer.
This table ranks reproducible LINC00555 RNA expression–survival associations across cancer types. High LINC00555 expression shows unfavorable associations in UCEC, OV, READ and LIHC, but favorable associations in KIRC and MESO. The UCEC Kaplan–Meier curve shows clear separation, with the high-expression group declining faster, consistent with the unfavorable association (log-rank p = .004). Together, the overview and detailed table identify UCEC as the clearest survival context for LINC00555 RNA expression.
This table summarizes LINC00555 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 KIRC for RNA.
This table ranks reproducible tumor–normal expression differences for LINC00555. A negative fold-change indicates higher expression in normal tissue than in tumor tissue. LINC00555 shows lower tumor expression in KIRC, COAD, THCA and KICH and higher tumor expression in STAD. The KIRC box plot shows higher LINC00555 RNA expression in normal versus tumor tissue (log2 FC = −0.108, t-test p < 0.001).
This table shows molecular features associated with LINC00555 in patient tissues and cancer cell lines. In patient samples, LINC00555 shows the broadest associations at the RNA and protein expression levels, with STAD recurring as the lineage with the largest associated feature set.
