KLHL6
Overview
KLHL6 (Kelch-Like Family Member 6) encodes a substrate adaptor for the BCR-ABL1 E3 ubiquitin ligase complex involved in B-cell receptor signaling. In cancer genomics, KLHL6 mutations in DLBCL show mutual exclusivity with TP53 mutations, suggesting non-overlapping functional roles in lymphomagenesis.
Alterations observed in the corpus
- Mutually exclusive with TP53 mutations in DLBCL (1001-patient cohort treated with rituximab-containing regimens); TP53 is CRISPR-enriched (loss increases fitness) while KLHL6 shows a distinct pattern. PMID:28985567
Cancer types (linked)
- DLBCL NOS: KLHL6 mutations are part of the 150 recurrently mutated driver gene landscape in DLBCL; mutual exclusivity with TP53 is a defining co-mutation pattern in this study. PMID:28985567
Co-occurrence and mutual exclusivity
- Mutually exclusive with TP53 mutations in DLBCL. PMID:28985567
Therapeutic relevance
- No direct targeted therapy against KLHL6 is reported in this corpus.
Open questions
- The mechanistic basis of KLHL6 and TP53 mutual exclusivity in DLBCL pathogenesis is not detailed; whether they represent convergent or divergent oncogenic pathways requires functional investigation. PMID:28985567
Sources
This page was processed by crosslinker on 2026-05-15.