NT5C2
Overview
NT5C2 encodes a cytosolic 5’-nucleotidase implicated in thiopurine resistance in relapsed ALL. In the corpus it appears as a relapse-associated gene in infant ALL PMID:25730765.
Alterations observed in the corpus
- Relapse-associated mutations identified in infant ALL PMID:25730765.
- NT5C2 D407Y pharmacogenomic variant in relapsed B-cell ALL (BLL) conferring resistance to nucleoside-analog therapy; informed salvage regimen choice in a pediatric precision-oncology cohort PMID:28007021
Cancer types (linked)
- BLLKMT2A: NT5C2 mutations observed at relapse PMID:25730765.
Co-occurrence and mutual exclusivity
- Not reported in this corpus.
Therapeutic relevance
- Relevance to thiopurine-based maintenance therapy resistance is implied by relapse enrichment PMID:25730765.
Open questions
- Whether NT5C2 mutations are selected during maintenance therapy in infant MLL-R ALL specifically PMID:25730765.
Sources
This page was processed by entity-page-writer on 2026-04-08. - PMID:28007021
This page was processed by entity-page-writer on 2026-05-15.