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Gene

MPL

MPL is a gene biomarker in the evidence tier "Cancer actionable (CGI)". This page lists evidence by type: Assay-provider ledger (3), Actionable biomarkers (1), Trial mentions (284), and 6 more evidence types, each linked to its source.

Ensembl ENSG00000117400 UniProt P40238 Matched to Ensembl and UniProt
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Assay-provider ledger Assay-provider ledger 3 Actionable biomarkers Actionable biomarkers 1 Trial mentions Trial mentions 284 Target-disease associations Target-disease associations 535 Vendor sourcing Vendor sourcing 1,013 Trial-cited literature Trial-cited literature 361 Protein variant mentions Protein variant mentions 33 Literature-extracted relations Literature-extracted relations 107 Assay-provider ledger Assay-provider ledger 3 Actionable biomarkers Actionable biomarkers 1 Trial mentions Trial mentions 284 Target-disease associations Target-disease associations 535 Vendor sourcing Vendor sourcing 1,013 Trial-cited literature Trial-cited literature 361 Protein variant mentions Protein variant mentions 33 Literature-extracted relations Literature-extracted relations 107

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 MPL. 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: 1 with a planned future start.

Publication mentions: plotted from 1990 to 2023, the years our matched corpus covers. Not plotted: 13 at the structurally incomplete recent edge.

The yearly numbers
MPL 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 33 of 8,738 0.38% not measured
2025 41 of 8,875 0.46% not measured
2024 15 of 8,597 0.17% not measured
2023 18 of 8,275 0.22% 30 of 11,460 0.26%
2022 18 of 8,285 0.22% 34 of 13,598 0.25%
2021 15 of 8,692 0.17% 36 of 15,045 0.24%
2020 7 of 7,640 0.09% 23 of 14,459 0.16%
2019 13 of 7,300 0.18% 35 of 12,159 0.29%
2018 10 of 6,927 0.14% 35 of 11,854 0.30%
2017 9 of 6,558 0.14% 25 of 11,595 0.22%

Assay-provider ledger (3)

Shown in this order: most recent publication first.

Assay-provider ledger
Company Provider class Validation Papers Most recent publication
AmpliSeq Reagent supplier No clinical or analytical validation recorded for this pair 1 September 01, 2016
Ion Torrent Personal Genome Machine Reagent supplier No clinical or analytical validation recorded for this pair 1 September 01, 2016
Illumina Unclassified Clinical validationAnalytical validation 1 January 22, 2016

Actionable biomarkers (1)

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

Actionable biomarkers
Alteration Drug Response Disease Source
MPL (W515F) Jak Inhibitors response-associated Myelodysplastic/Myeloproliferative Neoplasm Cancer Genome Interpreter

Trial mentions (284)

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

Trial mentions
Trial Source
NCT02823210 Trial biospecimen (AACT)
NCT00000419 Trial eligibility (AACT)
NCT01556945 Trial eligibility (AACT)
NCT07017725 Trial eligibility (AACT)
NCT00258635 Trial eligibility (AACT)

Target-disease associations (535)

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

Target-disease associations
Disease Therapeutic area Source
Abnormal bleeding phenotype Variant curation (ClinVar / EVA)
Acute Leukemia cancer or benign tumor Literature (Europe PMC)
Adult-onset autosomal recessive sideroblastic anemia genetic, familial or congenital disease Mouse knockout (IMPC)
Aicardi-Goutieres syndrome 6 genetic, familial or congenital disease Mouse knockout (IMPC)
Aicardi-Goutières syndrome genetic, familial or congenital disease Mouse knockout (IMPC)

Vendor sourcing (1,013)

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. Frameshift: predicted to result in a loss or disruption of normal protein function through protein ... View ClinVar record SCV002520954.1
ARUP Laboratories (United States) Testing lab / CRO (runs the assay) Clinical-testing interpretation submitted (ClinVar)ClinVar clinical-testing submission The MPL c.1653+1del variant (rs755257605, ClinVar Variation ID 632897), also known as c.1653del, is reported in the literature as compound heterozygous varia... View ClinVar record SCV005876210.1
AUSL Romagna Rimini Trial sponsor Named in trial inclusion criteriaTrial eligibility criteria : 1. Diagnosis of one of the following Ph-negative myeloproliferative neoplasms: polycythemia vera, essential thrombocythemia, idiopathic myelofibrosis,... View trial NCT06159816
AUSL Romagna Rimini Trial sponsor Mentioned in trial textTrial free-text mention MPL View trial NCT06159816
Abbisko Therapeutics Co., Ltd. (China) Trial collaborator Named in trial inclusion criteriaTrial eligibility criteria : * 1.Patient should understand, sign, and date the written voluntary informed consent form prior to any protocol-specific procedures performed. Patient sho... View trial NCT07010497

Trial-cited literature (361)

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

Trial-cited literature
Publication Journal Year Citations
Hetrombopag Added to Cyclosporine as the First-Line Treatment for Patients With Non-Severe Aplastic Anemia: A Phase 2 Multicenter Trial. American journal of hematology 2026 1
Avatrombopag for the treatment of children and adolescents with immune thrombocytopenia (AVA-PED-301): a multicentre, randomised, double-blind, placebo-controlled, phase 3b study. The Lancet. Haematology 2025 9
Eltrombopag for Newly Diagnosed Pediatric Immune Thrombocytopenia Requiring Treatment: The PINES Randomized Clinical Trial. JAMA 2025 5
Long-term follow-up of the STOPAGO study. Blood 2025 4
Ianalumab plus Eltrombopag in Immune Thrombocytopenia. The New England journal of medicine 2025 3

Protein variant mentions (33)

Shown in this order: alphabetical by variant.

Protein variant mentions
Variant Distinct papers Year range Sample papers
p.A58V 1 2015 PMID 25741868
p.E247K 1 2022 PMID 35203879
p.F147L 1 2022 PMID 35203879
p.G131S 1 2023 PMID 37647632
p.G238C 1 2015 PMID 25741868

Literature-extracted relations (107)

Shown in this order: chemicals, then diseases.

Literature-extracted relations
Related entity Kind Source relation label Paper Year
RITUXIMAB Chemical negative_correlate Thrombopoietin receptor agonists and rituximab for treatment of pediatric immune thrombocytopenia: A systematic review and meta-analysis of prospective clinical trials. 2022
Anemia, Aplastic Disease associate Hetrombopag Added to Cyclosporine as the First-Line Treatment for Patients With Non-Severe Aplastic Anemia: A Phase 2 Multicenter Trial. 2026
Purpura, Thrombocytopenic, Idiopathic Disease associate Long-term follow-up of the STOPAGO study. 2025
Thrombocytopenia Disease associate Romiplostim in chemotherapy-induced thrombocytopenia: A review of the literature. 2024
Purpura, Thrombocytopenic, Idiopathic Disease associate Efficacy and safety of sovleplenib (HMPL-523) in adult patients with chronic primary immune thrombocytopenia in China (ESLIM-01): a randomised, double-blind, placebo-controlled, phase 3 study. 2024

Organizations publishing (457)

Shown in this order: most papers first.

Organizations publishing
Organization Type Papers Years
Mass General Brigham Hospital 21 2006 to 2025
Mayo Clinic Hospital 20 2009 to 2023
University of Florence Academic 18 2013 to 2023
Harvard Medical School Academic 17 2006 to 2025
Memorial Sloan Kettering Cancer Center Hospital 17 2015 to 2024

Where MPL 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
  • integumentary system disease
  • measurement
  • phenotype

471 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