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Gene

SMARCA4

SMARCA4 is a gene biomarker in the evidence tier "Cancer actionable (CGI)". This page lists evidence by type: Assay-provider ledger (23), Actionable biomarkers (2), Trial mentions (44), and 6 more evidence types, each linked to its source.

Ensembl ENSG00000127616 UniProt P51532 Matched to Ensembl and UniProt
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Assay-provider ledger Assay-provider ledger 23 Actionable biomarkers Actionable biomarkers 2 Trial mentions Trial mentions 44 Target-disease associations Target-disease associations 706 Vendor sourcing Vendor sourcing 188 Trial-cited literature Trial-cited literature 166 Protein variant mentions Protein variant mentions 287 Literature-extracted relations Literature-extracted relations 25 Assay-provider ledger Assay-provider ledger 23 Actionable biomarkers Actionable biomarkers 2 Trial mentions Trial mentions 44 Target-disease associations Target-disease associations 706 Vendor sourcing Vendor sourcing 188 Trial-cited literature Trial-cited literature 166 Protein variant mentions Protein variant mentions 287 Literature-extracted relations Literature-extracted relations 25

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.

Get the SMARCA4 report as a PDF

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 SMARCA4. 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 no date at all.

Publication mentions: plotted from 1990 to 2023, the years our matched corpus covers. Not plotted: 8 at the structurally incomplete recent edge.

The yearly numbers
SMARCA4 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 7 of 8,738 0.08% not measured
2025 7 of 8,875 0.08% not measured
2024 4 of 8,597 0.05% not measured
2023 4 of 8,275 0.05% 15 of 11,460 0.13%
2022 3 of 8,285 0.04% 14 of 13,598 0.10%
2021 5 of 8,692 0.06% 27 of 15,045 0.18%
2020 3 of 7,640 0.04% 14 of 14,459 0.10%
2019 2 of 7,300 0.03% 15 of 12,159 0.12%
2018 1 of 6,927 0.01% 12 of 11,854 0.10%
2017 1 of 6,558 0.02% 11 of 11,595 0.09%

Assay-provider ledger (23)

Shown in this order: most recent publication first.

Assay-provider ledger
Company Provider class Validation Papers Most recent publication
Ventana Roche Unclassified Clinical validation 1 December 01, 2021
ABCAM Reagent supplier Clinical validationAnalytical validation 2 July 01, 2021 +1 undated
Atlas Antibodies Reagent supplier No clinical or analytical validation recorded for this pair 1 July 01, 2021
BD PharMingen Reagent supplier No clinical or analytical validation recorded for this pair 1 July 01, 2021
BioGenex Reagent supplier No clinical or analytical validation recorded for this pair 1 July 01, 2021

Actionable biomarkers (2)

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

Actionable biomarkers
Alteration Drug Response Disease Source
SMARCA4 oncogenic mutation Ezh2 Inhibitors response-associated ovarian carcinoma Cancer Genome Interpreter
SMARCA4 deletion Ezh2 Inhibitors response-associated ovarian carcinoma Cancer Genome Interpreter

Trial mentions (44)

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

Trial mentions
Trial Source
NCT04779151 Trial eligibility (AACT)
NCT05639751 Trial eligibility (AACT)
NCT04879017 Trial eligibility (AACT)
NCT07257055 Trial eligibility (AACT)
NCT07447076 Trial eligibility (AACT)

Target-disease associations (706)

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

Target-disease associations
Disease Therapeutic area Source
15q11.2 microdeletion syndrome genetic, familial or congenital disease Mouse knockout (IMPC)
16p13.11 microduplication syndrome genetic, familial or congenital disease Mouse knockout (IMPC)
22q11.2 deletion syndrome cardiovascular disease Mouse knockout (IMPC)
AIDS genetic, familial or congenital disease Literature (Europe PMC)
Abnormality of the gastrointestinal tract phenotype GWAS credible sets

Vendor sourcing (188)

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 SCV002059120.2
900th Hospital of PLA Joint Logistic Support Force Trial collaborator Named in trial inclusion criteriaTrial eligibility criteria : 1. Patients with pathologically confirmed NSCLC, meeting the following criteria based on the IASLC 9th Edition Lung Cancer TNM Staging System (Internation... View trial NCT07093762
900th Hospital of PLA Joint Logistic Support Force Trial collaborator Mentioned in trial textTrial free-text mention SMARCA4 View trial NCT07093762
ARUP Laboratories (United States) Testing lab / CRO (runs the assay) Clinical-testing interpretation submitted (ClinVar)ClinVar clinical-testing submission The SMARCA4 c.3436G>A; p.Gly1146Ser variant (rs200007170), to our knowledge, is not reported in the medical literature but is reported in ClinVar (Variation ... View ClinVar record SCV005875863.1
Acerta Pharma BV (Netherlands) Trial collaborator Named in trial inclusion criteriaTrial eligibility criteria : 1. Confirmed diagnosis of mantle cell lymphoma by hematopathology. MCL should have CD20 positivity (by flow or IHC in tissue or in BM) with presence of ch... View trial NCT05495464

Trial-cited literature (166)

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

Trial-cited literature
Publication Journal Year Citations
Precision Medicine Program in Chinese Pediatric Patients With Sarcoma. JCO precision oncology 2026 0
A Phase I Study of FHD-286, a Dual BRG1/BRM (SMARCA4/SMARCA2) Inhibitor, in Patients with Advanced Myeloid Malignancies. Clinical cancer research : an official journal of the American Association for Cancer Research 2025 11
A phase II trial of mTORC1/2 inhibition in STK11 deficient non small cell lung cancer. NPJ precision oncology 2025 7
Clinical and molecular characteristics of paediatric mature B-cell acute lymphocytic leukaemia and non-Hodgkin lymphoma with bone marrow involvement: A joint study between the CCCG leukaemia and lymphoma groups. British journal of haematology 2025 2
Mucin 16-Directed Therapy in Pediatric Sarcomas: Case Evidence of Ubamatamab Efficacy in Epithelioid Sarcoma and Its Implications for Other Sarcoma Subtypes. JCO precision oncology 2025 0

Protein variant mentions (287)

Shown in this order: alphabetical by variant.

Protein variant mentions
Variant Distinct papers Year range Sample papers
p.A1002V 1 2015 PMID 25741868
p.A104V 1 2015 PMID 25741868
p.A1094T 1 2015 PMID 25741868
p.A1117S 1 2015 PMID 25741868
p.A1186V 1 2015 PMID 25741868

Literature-extracted relations (25)

Shown in this order: chemicals, then diseases.

Literature-extracted relations
Related entity Kind Source relation label Paper Year
Disorders of Sex Development Disease associate A Phase I Study of FHD-286, a Dual BRG1/BRM (SMARCA4/SMARCA2) Inhibitor, in Patients with Advanced Myeloid Malignancies. 2025
Leukemia, Myeloid Disease associate A Phase I Study of FHD-286, a Dual BRG1/BRM (SMARCA4/SMARCA2) Inhibitor, in Patients with Advanced Myeloid Malignancies. 2025
Neoplasms Disease associate A Phase I Study of FHD-286, a Dual BRG1/BRM (SMARCA4/SMARCA2) Inhibitor, in Patients with Advanced Myeloid Malignancies. 2025
Carcinoma Disease associate Molecularly Defined Thoracic Neoplasms. 2024
Neoplasms Disease associate Molecularly Defined Thoracic Neoplasms. 2024

Organizations publishing (275)

Shown in this order: most papers first.

Organizations publishing
Organization Type Papers Years
Memorial Sloan Kettering Cancer Center Hospital 13 2015 to 2025
Government of the United States of America Government 10 2014 to 2023
The University of Texas System Academic 9 2013 to 2025
University of London Academic 9 2009 to 2025
Harvard Medical School Academic 8 2010 to 2023

Where SMARCA4 appears

  • biological_process
  • cancer or benign tumor
  • cardiovascular disease
  • disorder of ear
  • 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
  • measurement
  • medical procedure
  • musculoskeletal or connective tissue disease
  • nervous system disease
  • nutritional or metabolic disease
  • phenotype
  • respiratory or thoracic disease
  • urinary system disease

610 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