FAM90A1

Mutation & survival
SurvivalMutationKaplan–Meier · TCGA cohorts

Across TCGA pan-cancer cohorts, FAM90A1 Mutation is linked to patient survival in 5 of 34 cancer types, making it a survival-associated FAM90A1 data layer compared with 18 for mass-spec protein.

The strongest signal is observed in rectum adenocarcinoma (READ), where higher FAM90A1 Mutation is associated with worse overall survival. In most high-consensus cancer types, elevated FAM90A1 expression acts as an unfavorable survival marker, although some lineages such as UCEC show a favorable association.

READ, BRCA, and HNSC are the cancer types where FAM90A1 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
READOSMedianAll0.1730.828<.00132view →
BRCAOSMedianIII,IV0.1060.906<.00128view →
HNSCOSMedianIV0.2040.641.0206view →
BLCAOSMedianAll0.2380.597.0406view →
UCECDFSMedianII,III,IV0.9220.440.0344view →
Pink = unfavorable, green = favorable. Showing the 5 strongest of 5 lineages.

FAM90A1–READ (OS)

Kaplan–Meier survival curve for FAM90A1 mutant vs wild-type samples in READ.

Open the READ breakdown →

Exploration