Q-omics provides the consensus-scored SH3BP1 profile across patient tissues and cancer cell-line models. SH3BP1 expression is associated with patient survival in 25 of 34 cancer types, with the highest sampling consensus in STAD. Among the 18 cancer types available for tumor–normal comparison, SH3BP1 is differentially expressed in 14, with the highest sampling consensus in KIRC. Additionally, SH3BP1 protein abundance shows 18,951 significant protein co-abundance associations, with the highest sampling consensus in GBM. Together, these results highlight STAD, KIRC, and GBM as cancer lineages where SH3BP1 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 SH3BP1 — synthetic lethality, tumor antigen, and pembrolizumab response.
This table summarizes SH3BP1 survival associations across molecular data types. SH3BP1 RNA expression shows survival associations in the most cancer types (25), 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 SH3BP1 RNA expression–survival associations across cancer types. High SH3BP1 expression shows unfavorable associations in KIRC, HNSC and LAML, but favorable associations in STAD, SCLC and PAAD. The STAD 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 STAD as the clearest survival context for SH3BP1 RNA expression.
This table summarizes SH3BP1 tumor–normal expression differences by data type. RNA shows broader differences across cancer types, with a lineage consensus of 14, while mass-spec protein shows differences in 5. The strongest signals are observed in KIRC for RNA and CCRCC for protein.
This table ranks reproducible tumor–normal expression differences for SH3BP1. A negative fold-change indicates higher expression in normal tissue than in tumor tissue. SH3BP1 shows lower tumor expression in COAD and higher tumor expression in KIRC, THCA, HNSC, KIRP and STAD. The KIRC box plot shows higher SH3BP1 RNA expression in tumor versus normal tissue (log2 FC = +1.414, t-test p < 0.001).
This table shows molecular features associated with SH3BP1 in patient tissues and cancer cell lines. In patient samples, SH3BP1 shows the broadest associations at the RNA and protein expression levels, with GBM recurring as the lineage with the largest associated feature set. In cancer cell lines, SH3BP1 RNA and mutation anchors are most strongly linked to RNA-expression features, especially in PANCREAS, while CRISPR and shRNA rows add functional-dependency signals in LARGE_INTESTINE and BLOOD_Leukemia.
