IRX4

Mutation & survival
SurvivalMutationKaplan–Meier · TCGA cohorts

Across TCGA pan-cancer cohorts, IRX4 Mutation is linked to patient survival in 6 of 34 cancer types, making it a survival-associated IRX4 data layer compared with 16 for mass-spec protein.

The strongest signal is observed in adrenocortical carcinoma (ACC), where higher IRX4 Mutation is associated with worse overall survival. In most high-consensus cancer types, elevated IRX4 expression acts as an unfavorable survival marker.

ACC, LUSC, and PRAD are the cancer types where IRX4 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.
LineageMeasureSplitStageAUC1
high
AUC2
low
pSampling consensus
ACCOSMedianAll0.1450.888<.00145view →
LUSCOSMedianAll0.1780.762.00315view →
PRADDFSMedianAll0.0850.774<.0016view →
UCECOSMedianIV0.2310.592.0366view →
LIHCDFSMedianII,III,IV0.0440.427<.0016view →
SKCMOSMedianAll0.3330.780.0463view →
Pink = unfavorable, green = favorable. Showing the 6 strongest of 6 lineages.

IRX4–ACC (OS)

Kaplan–Meier survival curve for IRX4 mutant vs wild-type samples in ACC.

Open the ACC breakdown →

Exploration