Q-omics provides the consensus-scored GULP1 profile across patient tissues and cancer cell-line models. GULP1 expression is associated with patient survival in 26 of 34 cancer types, with the highest sampling consensus in STAD. Among the 18 cancer types available for tumor–normal comparison, GULP1 is differentially expressed in 13, with the highest sampling consensus in KIRC. Additionally, GULP1 RNA expression shows 18,932 significant gene co-expression associations, with the highest sampling consensus in UVM. Together, these results highlight STAD, KIRC, and UVM as cancer lineages where GULP1 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 GULP1 — synthetic lethality, tumor antigen, and pembrolizumab response.
This table summarizes GULP1 survival associations across molecular data types. GULP1 RNA expression shows survival associations in the most cancer types (26), followed by mutation status (1) and mass-spec protein abundance (7). The rightmost column indicates the cancer type with the highest sampling consensus for each molecular layer.
This table ranks reproducible GULP1 RNA expression–survival associations across cancer types. High GULP1 expression shows unfavorable associations in STAD, LIHC, BLCA, UVM, LUAD and ESCA. The STAD 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 STAD as the clearest survival context for GULP1 RNA expression.
This table summarizes GULP1 tumor–normal expression differences by data type. RNA shows broader differences across cancer types, with a lineage consensus of 13, while mass-spec protein shows differences in 6. The strongest signals are observed in KIRC for RNA and CCRCC for protein.
This table ranks reproducible tumor–normal expression differences for GULP1. A negative fold-change indicates higher expression in normal tissue than in tumor tissue. GULP1 shows lower tumor expression in KIRC, HNSC, THCA, UCEC and BLCA and higher tumor expression in KIRP. The KIRC box plot shows higher GULP1 RNA expression in normal versus tumor tissue (log2 FC = −0.763, t-test p < 0.001).
This table shows molecular features associated with GULP1 in patient tissues and cancer cell lines. In patient samples, GULP1 shows the broadest associations at the RNA and protein expression levels, with UVM recurring as the lineage with the largest associated feature set. In cancer cell lines, GULP1 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 SKIN and BONE.
