Fig. 4
From: The biological function and clinical significance of SF3B1 mutations in cancer
Venn diagrams showing SF3B1 mutation-associated aberrant splicing genes identified by RNAseq and validated by qRT-PCR in CLL, MDS, UM, and BC. At least 46 genes are produced by aberrant splicing events in SF3B1mut CLL, MDS, UM, and BC. Among them, BRD9 is shared by CLL, MDS and UM and TMEM14C by MDS, UM and BC. SEPT6 and SEPT2 are shared by CLL and MDS, ENOSF1 by MDS and UM, and DYNLL1 by MDS and BC