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Gene

ABL1

ABL1 is a gene biomarker in the evidence tier "Cancer actionable (CGI)". This page lists evidence by type: Assay-provider ledger (15), Actionable biomarkers (27), Trial mentions (762), and 6 more evidence types, each linked to its source.

Ensembl ENSG00000097007 UniProt P00519 Matched to Ensembl and UniProt
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Assay-provider ledger Assay-provider ledger 15 Actionable biomarkers Actionable biomarkers 27 Trial mentions Trial mentions 762 Target-disease associations Target-disease associations 693 Vendor sourcing Vendor sourcing 2,709 Trial-cited literature Trial-cited literature 938 Protein variant mentions Protein variant mentions 48 Literature-extracted relations Literature-extracted relations 422 Assay-provider ledger Assay-provider ledger 15 Actionable biomarkers Actionable biomarkers 27 Trial mentions Trial mentions 762 Target-disease associations Target-disease associations 693 Vendor sourcing Vendor sourcing 2,709 Trial-cited literature Trial-cited literature 938 Protein variant mentions Protein variant mentions 48 Literature-extracted relations Literature-extracted relations 422

Rows recorded per section (log scale)

1 more section with rows · 3 sections measured, none recorded

Cancer actionable (CGI)

Curated as clinically actionable in cancer by the Cancer Genome Interpreter.

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The PDF carries up to 50 rows of each section, where the page shows the first few, with the sources listed. Enter a work email and confirm it from the message we send, and the report follows by email.

Evidence over time

Share of that year: what fraction of the trials and papers our biomarker dictionary matched in a year mention ABL1. The denominator is documents that mention any gene, not every registered document, so improving the matcher moves both halves and never rewrites history. Gene named in free-text trial records. A mention, not a validated biomarker. Actionable-biomarker and target-disease-association evidence carries no date in our sources, so it is not on this chart. Publication mentions cover only papers cited by a registered clinical trial, not all of PubMed.

Trial mentions: plotted from 1990 to 2026, the years our matched corpus covers. Not plotted: 3 with a planned future start and 7 with no date at all.

Publication mentions: plotted from 1990 to 2023, the years our matched corpus covers. Not plotted: 3 dated before 1990 and 17 at the structurally incomplete recent edge.

The yearly numbers
ABL1 per year, by evidence type, the most recent 10 years, newest first; the chart covers 1990 to 2026. The share is of the trials and papers our biomarker dictionary matched that year, not of the literature at large, and a blank year is one our matched corpus does not cover at all.
Year Trial mentions Share of that year Publication mentions Share of that year
2026 54 of 8,738 0.62% not measured
2025 47 of 8,875 0.53% not measured
2024 54 of 8,597 0.63% not measured
2023 32 of 8,275 0.39% 34 of 11,460 0.30%
2022 37 of 8,285 0.45% 48 of 13,598 0.35%
2021 41 of 8,692 0.47% 59 of 15,045 0.39%
2020 37 of 7,640 0.48% 53 of 14,459 0.37%
2019 47 of 7,300 0.64% 49 of 12,159 0.40%
2018 40 of 6,927 0.58% 47 of 11,854 0.40%
2017 41 of 6,558 0.63% 64 of 11,595 0.55%

Assay-provider ledger (15)

Shown in this order: most recent publication first.

Assay-provider ledger
Company Provider class Validation Papers Most recent publication
Moroccan Foundation for Advanced Science Innovation and Research (MASCIR) Not a company Clinical validationAnalytical validation 1 July 01, 2026
ArcherDX Unclassified Clinical validationAnalytical validation 1 February 01, 2019
Illumina Unclassified Clinical validationAnalytical validation 2 February 01, 2019
QIAGEN Reagent supplier Clinical validationAnalytical validation 2 February 01, 2019
RainDance Technologies Reagent supplier Clinical validationAnalytical validation 1 February 01, 2019

Actionable biomarkers (27)

Shown in this order: fixed catalogue order, not ranked.

Actionable biomarkers
Alteration Drug Response Disease Source
ABL1-BCR fusion Dasatinib response-associated acute lymphoblastic leukemia Cancer Genome Interpreter
ABL1-BCR fusion Venetoclax response-associated acute lymphoblastic leukemia Cancer Genome Interpreter
ABL1 (T315I) Ponatinib response-associated acute lymphoblastic leukemia Cancer Genome Interpreter
ABL1-BCR fusion Ponatinib response-associated acute lymphoblastic leukemia Cancer Genome Interpreter
ABL1-BCR fusion Imatinib response-associated acute lymphoblastic leukemia Cancer Genome Interpreter

Trial mentions (762)

Shown in this order: fixed catalogue order, not by date.

Trial mentions
Trial Source
NCT01215487 Trial biospecimen (AACT)
NCT00052520 Trial eligibility (AACT)
NCT04544592 Trial eligibility (AACT)
NCT03249870 Trial eligibility (AACT)
NCT01657604 Trial eligibility (AACT)

Target-disease associations (693)

Shown in this order: fixed catalogue order, not ranked.

Target-disease associations
Disease Therapeutic area Source
ATTRV122I amyloidosis cardiovascular disease Mouse knockout (IMPC)
Abnormal skeletal morphology phenotype Variant curation (ClinVar / EVA)
Abnormality of the skeletal system phenotype GWAS credible sets
Acute Leukemia cancer or benign tumor Literature (Europe PMC)
Adenoid Cystic Breast Carcinoma cancer or benign tumor Cancer Gene Census

Vendor sourcing (2,709)

Shown in this order: alphabetical by organization.

Vendor sourcing
Organization Role Tier Evidence Citation
3billion, Inc. (South Korea) Testing lab / CRO (runs the assay) Clinical-testing interpretation submitted (ClinVar)ClinVar clinical-testing submission The variant is not observed in the gnomAD v2.1.1 dataset. Predicted Consequence/Location: Missense variant In silico tool predictions suggest damaging effect... View ClinVar record SCV002012192.2
A&D Instruments, Ltd Trial collaborator Named in trial inclusion criteriaTrial eligibility criteria (non-exclusive; when CRP test is unavailable in medical records) associated with high or very high cardiovascular (CV) toxicity risk factors (according to th... View trial NCT06778122
A&D Instruments, Ltd Trial collaborator Mentioned in trial textTrial free-text mention ABL View trial NCT06778122
ADIR, a Servier Group company Trial collaborator Named in trial exclusion criteriaTrial eligibility criteria : * Mature B-cell ALL ; Philadelphia chromosome-positive (Ph+) or BCR-ABL1-positive ALL * Preexisting known coagulopathy ; * History of pancreatitis; * Cont... View trial NCT04067518
ADIR, a Servier Group company Trial collaborator Mentioned in trial textTrial free-text mention ABL1 View trial NCT04067518

Trial-cited literature (938)

Shown in this order: newest first, then most cited.

Trial-cited literature
Publication Journal Year Citations
Molecular characterization and predictors of relapse in patients with Ph + ALL after frontline ponatinib and blinatumomab. Journal of hematology & oncology 2025 22
A Phase I/II Trial of Ruxolitinib with Chemotherapy for Patients with Relapsed and/or Refractory Philadelphia-like Acute Lymphoblastic Leukemia. Clinical lymphoma, myeloma & leukemia 2025 8
Identification of anticancer drugs associated to cancer therapy-related cardiac dysfunction: a VigiBase® disproportionality analysis. European heart journal. Cardiovascular pharmacotherapy 2025 3
Outcome of children with B-cell acute lymphoblastic leukemia with hypodiploidy or BCR::ABL1 fusion undergoing allogeneic HSCT. Blood 2025 2
Measuring treatment burden related to general practice in patients with multimorbidity: development and validation of a PROM. Family medicine and community health 2025 2

Protein variant mentions (48)

Shown in this order: alphabetical by variant.

Protein variant mentions
Variant Distinct papers Year range Sample papers
p.A337T 1 2015 PMID 25741868
p.A433T 1 2015 PMID 25741868
p.E1037Q 1 2015 PMID 25741868
p.E255Q 1 2013 PMID 23468307
p.E255V 11 2010 to 2025 PMID 40369607, PMID 37738125, PMID 35643868

Literature-extracted relations (422)

Shown in this order: chemicals, then diseases.

Literature-extracted relations
Related entity Kind Source relation label Paper Year
Levofloxacin Chemical associate Clinical evaluation of a commercial culture-free targeted next-generation sequencing test for diagnosis of drug-resistant tuberculosis. 2025
DASATINIB Chemical negative_correlate Dasatinib with intensive chemotherapy in de novo paediatric Philadelphia chromosome-positive acute lymphoblastic leukaemia (CA180-372/COG AALL1122): a single-arm, multicentre, phase 2 trial. 2023
DASATINIB Chemical negative_correlate Low-Dose Dasatinib (50 mg Daily) Frontline Therapy in Newly Diagnosed Chronic Phase Chronic Myeloid Leukemia: 5-Year Follow-Up Results. 2023
Imatinib Chemical negative_correlate Ponatinib, chemotherapy, and transplant in adults with Philadelphia chromosome-positive acute lymphoblastic leukemia. 2022
DASATINIB Chemical negative_correlate Dasatinib dose optimisation based on therapeutic drug monitoring reduces pleural effusion rates in chronic myeloid leukaemia patients. 2021

Organizations publishing (574)

Shown in this order: most papers first.

Organizations publishing
Organization Type Papers Years
The University of Texas System Academic 59 2002 to 2025
Memorial Sloan Kettering Cancer Center Hospital 34 2000 to 2022
Dana-Farber Cancer Institute Other 32 2000 to 2023
Novant Health Hospital 32 2002 to 2023
Government of the United States of America Government 25 1998 to 2023

Where ABL1 appears

  • biological_process
  • cancer or benign tumor
  • cardiovascular disease
  • disorder of visual system
  • endocrine system disease
  • gastrointestinal disease
  • genetic, familial or congenital disease
  • hematologic disease
  • immune system disease
  • infectious disease
  • injury, poisoning or other complication
  • integumentary system disease
  • measurement
  • musculoskeletal or connective tissue disease
  • nervous system disease
  • nutritional or metabolic disease
  • phenotype
  • reproductive system or breast disease
  • respiratory or thoracic disease
  • urinary system disease

586 diseases touched.

Not on this page

Checked, with nothing recorded for this biomarker: fda companion diagnostic assertions, fda biomarker qualification projects, and human sample screening reference.

Browse all biomarker evidence pages