RPL27A

Across TCGA pan-cancer cohorts, RPL27A Mutation is linked to patient survival in 4 of 34 cancer types, making it a survival-associated RPL27A data layer compared with 22 for mass-spec protein and 6 for mass-spec protein.

The strongest signal is observed in colon adenocarcinoma (COAD), where higher RPL27A Mutation is associated with worse overall survival. In most high-consensus cancer types, elevated RPL27A expression acts as an unfavorable survival marker.

COAD, UCEC, and SARC are the cancer types where RPL27A Mutation most reproducibly stratifies survival.

Mutation survival associations by lineage

Ranked by sampling consensus. AUC1 and AUC2 indicate survival in the high- and low-expression groups, respectively; the lower AUC marks the poorer-surviving group. p-values are from the log-rank test.

Lineage	Measure	Split	Stage	AUC1 high	AUC2 low	p	Sampling consensus
COAD	OS	Median	All	0.103	0.801	<.001	24	view →
UCEC	OS	Median	IV	0.133	0.754	<.001	12	view →
SARC	DFS	Median	All	0.181	0.614	.006	6	view →
SKCM	DFS	Median	All	0.375	0.626	.006	5	view →

Pink = unfavorable, green = favorable. Showing the 4 strongest of 4 lineages.

RPL27A–COAD (OS)

Open the COAD breakdown →