ARHGAP23

Across TCGA pan-cancer cohorts, ARHGAP23 Mutation is linked to patient survival in 3 of 34 cancer types, making it a survival-associated ARHGAP23 data layer compared with 29 for mass-spec protein and 6 for mass-spec protein.

The strongest signal is observed in esophageal carcinoma (ESCA), where higher ARHGAP23 Mutation is associated with worse disease-free survival. In most high-consensus cancer types, elevated ARHGAP23 expression acts as an unfavorable survival marker.

ESCA, UCEC, and CHOL are the cancer types where ARHGAP23 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
ESCA	DFS	Median	All	0.162	0.546	<.001	18	view →
UCEC	OS	Median	IV	0.231	0.592	.036	6	view →
CHOL	OS	Median	All	0.155	0.725	.029	3	view →

Pink = unfavorable, green = favorable. Showing the 3 strongest of 3 lineages.

ARHGAP23–ESCA (DFS)

Open the ESCA breakdown →