Across TCGA pan-cancer cohorts, RN7SL408P RNA differs between tumor and matched normal tissue in 4 of 18 cancer types tested, making tumor–normal expression one of RN7SL408P’s most consistent transcriptional readouts.
The strongest signal is observed in prostate adenocarcinoma (PRAD), where RN7SL408P RNA is more highly expressed in tumor relative to normal tissue. In most cancer types RN7SL408P is over-expressed in tumor, although a few such as STAD and LUSC show the opposite, repressed pattern.
PRAD, STAD, and LUSC are the cancer types where RN7SL408P tumor–normal differential expression is most reproducible.