IL23R

Across TCGA pan-cancer cohorts, IL23R Mutation is linked to patient survival in 3 of 34 cancer types, making it a survival-associated IL23R data layer compared with 19 for mass-spec protein and 2 for mass-spec protein.

The strongest signal is observed in liver hepatocellular carcinoma (LIHC), where higher IL23R Mutation is associated with worse disease-free survival. In most high-consensus cancer types, elevated IL23R expression acts as an unfavorable survival marker.

LIHC, PRAD, and STAD are the cancer types where IL23R 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
LIHC	DFS	Median	All	0.115	0.557	.001	12	view →
PRAD	DFS	Median	All	0.107	0.886	<.001	6	view →
STAD	OS	Median	All	0.347	0.670	.049	3	view →

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

IL23R–LIHC (DFS)

Open the LIHC breakdown →