solute carrier family 1 member 4Genealiases: ASCT1 · SATT · SPATCCM
Q-omics provides the consensus-scored SLC1A4 profile across patient tissues and cancer cell-line models. SLC1A4 expression is associated with patient survival in 26 of 34 cancer types, with the highest sampling consensus in ACC. Among the 18 cancer types available for tumor–normal comparison, SLC1A4 is differentially expressed in 14, with the highest sampling consensus in KIRC. Additionally, SLC1A4 protein abundance shows 25,269 significant protein co-abundance associations, with the highest sampling consensus in GBM. Together, these results highlight ACC, KIRC, and GBM as cancer lineages where SLC1A4 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 SLC1A4 — synthetic lethality, tumor antigen, and pembrolizumab response.
This table summarizes SLC1A4 survival associations across molecular data types. SLC1A4 RNA expression shows survival associations in the most cancer types (26), followed by mutation status (4) and mass-spec protein abundance (6). The rightmost column indicates the cancer type with the highest sampling consensus for each molecular layer.
This table ranks reproducible SLC1A4 RNA expression–survival associations across cancer types. High SLC1A4 expression shows unfavorable associations in ACC, UVM, LIHC and KICH, but favorable associations in BRCA and LUAD. The ACC 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 ACC as the clearest survival context for SLC1A4 RNA expression.
This table summarizes SLC1A4 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 9. The strongest signals are observed in KIRC for RNA and CCRCC for protein.
This table ranks reproducible tumor–normal expression differences for SLC1A4. A negative fold-change indicates higher expression in normal tissue than in tumor tissue. SLC1A4 shows higher tumor expression in KIRC, HNSC, LUAD, COAD, KIRP and LIHC. The KIRC box plot shows higher SLC1A4 RNA expression in tumor versus normal tissue (log2 FC = +1.963, t-test p < 0.001).
This table shows molecular features associated with SLC1A4 in patient tissues and cancer cell lines. In patient samples, SLC1A4 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, SLC1A4 RNA and mutation anchors are most strongly linked to RNA-expression features, especially in LIVER, while CRISPR and shRNA rows add functional-dependency signals in PANCREAS and BLOOD_Leukemia.
