Q-omics provides the consensus-scored SHANK2-AS1 profile across patient tissues and cancer cell-line models. SHANK2-AS1 expression is associated with patient survival in 15 of 34 cancer types, with the highest sampling consensus in HNSC. Among the 18 cancer types available for tumor–normal comparison, SHANK2-AS1 is differentially expressed in 8, with the highest sampling consensus in THCA. Additionally, SHANK2-AS1 RNA expression shows 10,718 significant protein co-abundance associations, with the highest sampling consensus in GBM. Together, these results highlight HNSC, THCA, and GBM as cancer lineages where SHANK2-AS1 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 SHANK2-AS1 — synthetic lethality, tumor antigen, and pembrolizumab response.
This table summarizes SHANK2-AS1 survival associations across molecular data types. SHANK2-AS1 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 SHANK2-AS1 RNA expression–survival associations across cancer types. High SHANK2-AS1 expression shows unfavorable associations in HNSC, CESC, ACC, KIRP and DLBC, but favorable associations in LGG. The HNSC 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 HNSC as the clearest survival context for SHANK2-AS1 RNA expression.
This table summarizes SHANK2-AS1 tumor–normal expression differences by data type. RNA shows broader differences across cancer types, with a lineage consensus of 8. The strongest signals are observed in THCA for RNA.
This table ranks reproducible tumor–normal expression differences for SHANK2-AS1. A negative fold-change indicates higher expression in normal tissue than in tumor tissue. SHANK2-AS1 shows lower tumor expression in THCA, LUSC and LUAD and higher tumor expression in STAD, BRCA and BLCA. The THCA box plot shows higher SHANK2-AS1 RNA expression in normal versus tumor tissue (log2 FC = −0.092, t-test p < 0.001).
This table shows molecular features associated with SHANK2-AS1 in patient tissues and cancer cell lines. In patient samples, SHANK2-AS1 shows the broadest associations at the RNA and protein expression levels, with GBM recurring as the lineage with the largest associated feature set.
