Across TCGA pan-cancer cohorts, RN7SL233P RNA differs between tumor and matched normal tissue in 5 of 18 cancer types tested, making tumor–normal expression one of RN7SL233P’s most consistent transcriptional readouts.
The strongest signal is observed in stomach adenocarcinoma (STAD), where RN7SL233P RNA is more highly expressed in tumor relative to normal tissue. In most cancer types RN7SL233P is over-expressed in tumor, although a few such as KIRC and COAD show the opposite, repressed pattern.
STAD, CHOL, and KIRC are the cancer types where RN7SL233P tumor–normal differential expression is most reproducible.