BTBD9

Mutation & survival
SurvivalMutationKaplan–Meier · TCGA cohorts

Across TCGA pan-cancer cohorts, BTBD9 Mutation is linked to patient survival in 7 of 34 cancer types, making it a survival-associated BTBD9 data layer compared with 23 for mass-spec protein and 5 for mass-spec protein.

The strongest signal is observed in ovarian serous cystadenocarcinoma (OV), where higher BTBD9 Mutation is associated with worse disease-free survival. In most high-consensus cancer types, elevated BTBD9 expression acts as an unfavorable survival marker, although some lineages such as BLCA show a favorable association.

OV, DLBC, and STAD are the cancer types where BTBD9 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
OVDFSMedianII,III,IV0.1740.541.00918view →
DLBCOSMedianAll0.0530.936<.00112view →
STADOSMedianII,III,IV0.1830.660.00912view →
BLCADFSMedianAll1.0000.328.0389view →
PRADDFSMedianAll0.0850.774<.0016view →
UCECOSMedianIV0.2310.592.0366view →
SKCMDFSMedianIII,IV0.0460.648<.0014view →
Pink = unfavorable, green = favorable. Showing the 7 strongest of 7 lineages.

Exploration