PRRC2B

Mutation & survival
SurvivalMutationKaplan–Meier · TCGA cohorts

Across TCGA pan-cancer cohorts, PRRC2B Mutation is linked to patient survival in 13 of 34 cancer types, making it a survival-associated PRRC2B data layer compared with 23 for mass-spec protein and 5 for mass-spec protein.

The strongest signal is observed in kidney renal papillary cell carcinoma (KIRP), where higher PRRC2B Mutation is associated with worse overall survival. In most high-consensus cancer types, elevated PRRC2B expression acts as an unfavorable survival marker, although some lineages such as SKCM and COAD show a favorable association.

KIRP, ESCA, and KICH are the cancer types where PRRC2B 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
KIRPOSMedianAll0.1690.888<.00142view →
ESCAOSMedianII,III,IV0.1080.687<.00124view →
KICHDFSMedianAll0.1020.848.00413view →
TGCTOSMedianAll0.0690.968<.00112view →
SARCDFSMedianAll0.2170.617<.0016view →
PRADDFSMedianAll0.0850.774.0016view →
READDFSMedianAll0.2230.730.0066view →
UCECOSMedianIV0.2310.592.0366view →
LUADDFSMedianIV0.3420.893<.0016view →
LGGOSMedianAll0.2550.799.0173view →
ACCDFSMedianAll0.1950.748.0033view →
SKCMDFSMedianAll0.7650.609.0272view →
Pink = unfavorable, green = favorable. Showing the 12 strongest of 13 lineages.

PRRC2B–KIRP (OS)

Kaplan–Meier survival curve for PRRC2B mutant vs wild-type samples in KIRP.

Open the KIRP breakdown →

Exploration