RAP1GAP

Across TCGA pan-cancer cohorts, RAP1GAP Mutation is linked to patient survival in 5 of 34 cancer types, making it a survival-associated RAP1GAP data layer compared with 23 for mass-spec protein and 4 for mass-spec protein.

The strongest signal is observed in uterine corpus endometrial carcinoma (UCEC), where higher RAP1GAP Mutation is associated with better disease-free survival. In most high-consensus cancer types, elevated RAP1GAP expression acts as an unfavorable survival marker, although some lineages such as UCEC show a favorable association.

UCEC, CESC, and SKCM are the cancer types where RAP1GAP 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
UCEC	DFS	Median	All	1.000	0.625	.006	32	view →
CESC	DFS	Median	III,IV	0.191	0.634	.016	12	view →
SKCM	OS	Median	All	0.656	0.791	.011	8	view →
PRAD	OS	Median	All	0.369	0.887	<.001	6	view →
ACC	DFS	Median	All	0.195	0.748	.003	3	view →

Pink = unfavorable, green = favorable. Showing the 5 strongest of 5 lineages.

RAP1GAP–UCEC (DFS)

Open the UCEC breakdown →