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Gene

CBL

CBL is a gene biomarker in the evidence tier "Cancer actionable (CGI)". This page lists evidence by type: Assay-provider ledger (2), Actionable biomarkers (2), Trial mentions (32), and 6 more evidence types, each linked to its source.

Ensembl ENSG00000110395 UniProt P22681 Matched to Ensembl and UniProt
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Assay-provider ledger Assay-provider ledger 2 Actionable biomarkers Actionable biomarkers 2 Trial mentions Trial mentions 32 Target-disease associations Target-disease associations 590 Vendor sourcing Vendor sourcing 136 Trial-cited literature Trial-cited literature 165 Protein variant mentions Protein variant mentions 57 Literature-extracted relations Literature-extracted relations 18 Assay-provider ledger Assay-provider ledger 2 Actionable biomarkers Actionable biomarkers 2 Trial mentions Trial mentions 32 Target-disease associations Target-disease associations 590 Vendor sourcing Vendor sourcing 136 Trial-cited literature Trial-cited literature 165 Protein variant mentions Protein variant mentions 57 Literature-extracted relations Literature-extracted relations 18

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 CBL. 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.

Publication mentions: plotted from 1990 to 2023, the years our matched corpus covers. Not plotted: 6 at the structurally incomplete recent edge.

The yearly numbers
CBL 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 2 of 8,738 0.02% not measured
2025 6 of 8,875 0.07% not measured
2024 3 of 8,597 0.03% not measured
2023 5 of 8,275 0.06% 14 of 11,460 0.12%
2022 3 of 8,285 0.04% 15 of 13,598 0.11%
2021 4 of 8,692 0.05% 16 of 15,045 0.11%
2020 4 of 7,640 0.05% 14 of 14,459 0.10%
2019 1 of 7,300 0.01% 14 of 12,159 0.12%
2018 2 of 6,927 0.03% 16 of 11,854 0.13%
2017 0 of 6,558 0.00% 9 of 11,595 0.08%

Assay-provider ledger (2)

Shown in this order: most recent publication first.

Assay-provider ledger
Company Provider class Validation Papers Most recent publication
Agilent Reagent supplier No clinical or analytical validation recorded for this pair 1 February 20, 2015
Illumina Unclassified No clinical or analytical validation recorded for this pair 1 February 20, 2015

Actionable biomarkers (2)

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

Actionable biomarkers
Alteration Drug Response Disease Source
CBL (Y371H,C384R) Dasatinib response-associated Myelodysplastic/Myeloproliferative Neoplasm Cancer Genome Interpreter
CBL (Y371H,C384R) Jak Inhibitors response-associated Myelodysplastic/Myeloproliferative Neoplasm Cancer Genome Interpreter

Trial mentions (32)

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

Trial mentions
Trial Source
NCT02823210 Trial biospecimen (AACT)
NCT06284460 Trial eligibility (AACT)
NCT06247787 Trial eligibility (AACT)
NCT04409639 Trial eligibility (AACT)
NCT07032727 Trial eligibility (AACT)

Target-disease associations (590)

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

Target-disease associations
Disease Therapeutic area Source
AKT2-related familial partial lipodystrophy genetic, familial or congenital disease Mouse knockout (IMPC)
Abnormality of the cardiovascular system phenotype Variant curation (ClinVar / EVA)
Acute Leukemia cancer or benign tumor Literature (Europe PMC)
Adrenal Gland Neuroblastoma cancer or benign tumor Cancer Gene Census
Adult-onset autosomal recessive sideroblastic anemia genetic, familial or congenital disease Mouse knockout (IMPC)

Vendor sourcing (136)

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 v4.1.0 dataset. Predicted Consequence/Location: Canonical splice site: predicted to alter splicing and result in a ... View ClinVar record SCV002058377.2
ARUP Laboratories (United States) Testing lab / CRO (runs the assay) Clinical-testing interpretation submitted (ClinVar)ClinVar clinical-testing submission The CBL c.2606A>G; p.Tyr869Cys variant (rs758291160), to our knowledge, is not reported in the medical literature or gene specific databases. This variant is... View ClinVar record SCV004563269.1
AbbVie Inc. Trial collaborator Named in trial inclusion criteriaTrial eligibility criteria : * Ability to comprehend the investigational nature of the study and provide informed consent (i.e., participant or legally authorized representative \[LAR... View trial NCT06504459
AbbVie Inc. Trial collaborator Mentioned in trial textTrial free-text mention CBL View trial NCT06504459
Ambry Genetics (United States) Testing lab / CRO (runs the assay) Clinical-testing interpretation submitted (ClinVar)ClinVar clinical-testing submission The c.1210T>C (p.C404R) alteration is located in coding exon 8 of the CBL gene. This alteration results from a T to C substitution at nucleotide position 121... View ClinVar record SCV001444949.3

Trial-cited literature (165)

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

Trial-cited literature
Publication Journal Year Citations
Impact of Mutational Landscape and Burden on RBC Transfusion Response in Patients With Lower-Risk Myelodysplastic Syndromes (LR-MDS) in the COMMANDS Study. American journal of hematology 2026 0
Pharmacogenomics of the Etonogestrel Contraceptive Implant: A Genome-Wide Association Study of Steady-State Etonogestrel Concentrations. O&G open 2025 0
Sex-associated differences in frequencies and prognostic impact of recurrent genetic alterations in adult acute myeloid leukemia (Alliance, AMLCG). Leukemia 2024 35
Phase 1 study of azacitidine in combination with quizartinib in patients with FLT3 or CBL mutated MDS and MDS/MPN. Leukemia research 2024 8
Sitravatinib in patients with solid tumors selected by molecular alterations: results from a Phase Ib study. Future oncology (London, England) 2024 1

Protein variant mentions (57)

Shown in this order: alphabetical by variant.

Protein variant mentions
Variant Distinct papers Year range Sample papers
p.A757T 5 2013 to 2017 PMID 29296819, PMID 27069254, PMID 25741868
p.C401F 1 2015 PMID 25741868
p.C401R 1 2015 PMID 25741868
p.C404R 1 2018 PMID 29528181
p.C840W 1 2015 PMID 25741868

Literature-extracted relations (18)

Shown in this order: chemicals, then diseases.

Literature-extracted relations
Related entity Kind Source relation label Paper Year
Neoplasms Disease associate Sitravatinib in patients with solid tumors selected by molecular alterations: results from a Phase Ib study. 2024
Myelodysplastic Syndromes Disease associate Phase 1 study of azacitidine in combination with quizartinib in patients with FLT3 or CBL mutated MDS and MDS/MPN. 2024
Primary Immunodeficiency Diseases Disease associate Pediatric Evans syndrome is associated with a high frequency of potentially damaging variants in immune genes. 2019
Myelodysplastic Syndromes Disease associate Incorporation of mutations in five genes in the revised International Prognostic Scoring System can improve risk stratification in the patients with myelodysplastic syndrome. 2018
Myelodysplastic Syndromes Disease associate Myelodysplastic syndromes: Contemporary review and how we treat. 2016

Organizations publishing (262)

Shown in this order: most papers first.

Organizations publishing
Organization Type Papers Years
Government of the United States of America Government 14 2009 to 2024
Memorial Sloan Kettering Cancer Center Hospital 9 2012 to 2021
The University of Texas System Academic 7 2013 to 2026
University of California System Academic 7 2013 to 2024
University of Florence Academic 7 2013 to 2026

Where CBL appears

  • animal disease
  • 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
  • measurement
  • nervous system disease
  • nutritional or metabolic disease
  • phenotype
  • respiratory or thoracic disease

541 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