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abl1
ABL1
Non-receptor tyrosine kinase; fused with BCR in CML (t(9;22)) → constitutive BCR-ABL → RAS-MAPK, STAT5, and PI3K → leukemic proliferation. Imatinib, dasatinib, nilotinib are ABL inhibitors; asciminib (STAMP) and ponatinib overcome T315I gatekeeper resistance.
Entry Metadata
| Field | Value |
|---|---|
| ID | abl1 |
| Name | ABL1 |
| Status | draft |
| Last reviewed | 2026-06-06 |
| Atlas | 01-human |
| Scale | 03-molecular |
Cross-Atlas Connections
Sources
- Druker BJ, Talpaz M, Resta DJ, et al. Efficacy and safety of a specific inhibitor of the BCR-ABL tyrosine kinase in chronic myeloid leukemia. N Engl J Med. 2001;344(14):1031-1037. · PubMed 11287973
- Hochhaus A, Boquimpani C, Rea D, et al. Efficacy and safety results from ASCEMBL, a multicenter, open-label, phase 3 study of asciminib vs bosutinib in chronic-phase CML. Blood. 2021;138(Suppl 1):2160. · PubMed 34739052