long intergenic non-protein coding RNA 1716Genealiases: []
Q-omics provides the consensus-scored LINC01716 profile across patient tissues and cancer cell-line models. LINC01716 expression is associated with patient survival in 14 of 34 cancer types, with the highest sampling consensus in KICH. Among the 18 cancer types available for tumor–normal comparison, LINC01716 is differentially expressed in 1, with the highest sampling consensus in HNSC. Additionally, LINC01716 RNA expression shows 9,683 significant gene co-expression associations, with the highest sampling consensus in TGCT. Together, these results highlight KICH, HNSC, and TGCT as cancer lineages where LINC01716 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 LINC01716 — synthetic lethality, tumor antigen, and pembrolizumab response.
This table summarizes LINC01716 survival associations across molecular data types. LINC01716 RNA expression shows survival associations in the most cancer types (14). The rightmost column indicates the cancer type with the highest sampling consensus for each molecular layer.
This table ranks reproducible LINC01716 RNA expression–survival associations across cancer types. High LINC01716 expression shows unfavorable associations in KICH, KIRC, UCS, THYM and DLBC, but favorable associations in ESCA. The KICH 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 KICH as the clearest survival context for LINC01716 RNA expression.
This table summarizes LINC01716 tumor–normal expression differences by data type. RNA shows broader differences across cancer types, with a lineage consensus of 1. The strongest signals are observed in HNSC for RNA.
This table ranks reproducible tumor–normal expression differences for LINC01716. A negative fold-change indicates higher expression in normal tissue than in tumor tissue. LINC01716 shows higher tumor expression in HNSC. The HNSC box plot shows higher LINC01716 RNA expression in tumor versus normal tissue (log2 FC = +0.044, t-test p = .023).
This table shows molecular features associated with LINC01716 in patient tissues and cancer cell lines. In patient samples, LINC01716 shows the broadest associations at the RNA and protein expression levels, with TGCT recurring as the lineage with the largest associated feature set.
