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Gene

SMARCB1

SMARCB1 is a gene biomarker in the evidence tier "Cancer actionable (CGI)". This page lists evidence by type: Assay-provider ledger (36), Actionable biomarkers (3), Trial mentions (44), and 6 more evidence types, each linked to its source.

Ensembl ENSG00000099956 UniProt Q12824 Matched to Ensembl and UniProt
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Assay-provider ledger Assay-provider ledger 36 Actionable biomarkers Actionable biomarkers 3 Trial mentions Trial mentions 44 Target-disease associations Target-disease associations 454 Vendor sourcing Vendor sourcing 169 Trial-cited literature Trial-cited literature 124 Protein variant mentions Protein variant mentions 11 Literature-extracted relations Literature-extracted relations 17 Assay-provider ledger Assay-provider ledger 36 Actionable biomarkers Actionable biomarkers 3 Trial mentions Trial mentions 44 Target-disease associations Target-disease associations 454 Vendor sourcing Vendor sourcing 169 Trial-cited literature Trial-cited literature 124 Protein variant mentions Protein variant mentions 11 Literature-extracted relations Literature-extracted relations 17

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 SMARCB1. 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: 2 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
SMARCB1 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 5 of 8,738 0.06% not measured
2025 1 of 8,875 0.01% not measured
2024 3 of 8,597 0.03% not measured
2023 5 of 8,275 0.06% 8 of 11,460 0.07%
2022 5 of 8,285 0.06% 6 of 13,598 0.04%
2021 1 of 8,692 0.01% 12 of 15,045 0.08%
2020 4 of 7,640 0.05% 8 of 14,459 0.06%
2019 1 of 7,300 0.01% 13 of 12,159 0.11%
2018 4 of 6,927 0.06% 9 of 11,854 0.08%
2017 2 of 6,558 0.03% 8 of 11,595 0.07%

Assay-provider ledger (36)

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 4 July 01, 2021
Atlas Antibodies Reagent supplier Clinical validation 2 July 01, 2021
BD PharMingen Reagent supplier No clinical or analytical validation recorded for this pair 1 July 01, 2021
BioGenex Reagent supplier Clinical validation 2 July 01, 2021

Actionable biomarkers (3)

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

Actionable biomarkers
Alteration Drug Response Disease Source
SMARCB1 oncogenic mutation Hdac Inhibitors response-associated malignant rhabdoid tumour Cancer Genome Interpreter
SMARCB1 deletion Ezh2 Inhibitors response-associated malignant rhabdoid tumour Cancer Genome Interpreter
SMARCB1 oncogenic mutation Ezh2 Inhibitors response-associated malignant rhabdoid tumour Cancer Genome Interpreter

Trial mentions (44)

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

Trial mentions
Trial Source
NCT04416568 Trial eligibility (AACT)
NCT07438626 Trial eligibility (AACT)
NCT03375307 Trial eligibility (AACT)
NCT04266912 Trial eligibility (AACT)
NCT05684692 Trial eligibility (AACT)

Target-disease associations (454)

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

Target-disease associations
Disease Therapeutic area Source
APC-related attenuated familial adenomatous polyposis cancer or benign tumor Mouse knockout (IMPC)
Anal Squamous Cell Carcinoma cancer or benign tumor Cancer Gene Census
Anaplastic (Malignant) Meningioma cancer or benign tumor Cancer Gene Census
Andersen-Tawil syndrome genetic, familial or congenital disease Literature (Europe PMC)
Angiomatous Meningioma cancer or benign tumor Cancer Gene Census

Vendor sourcing (169)

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 Same nucleotide change resulting in same amino acid change has been previously reported as pathogenic/likely pathogeic with strong evidence (ClinVar VCV00021... View ClinVar record SCV002011943.1
ARUP Laboratories (United States) Testing lab / CRO (runs the assay) Clinical-testing interpretation submitted (ClinVar)ClinVar clinical-testing submission No supporting text recorded; see the citation. View ClinVar record SCV000605225.1
Ambry Genetics (United States) Testing lab / CRO (runs the assay) Clinical-testing interpretation submitted (ClinVar)ClinVar clinical-testing submission This alteration is classified as benign based on a combination of the following: seen in unaffected individuals, population frequency, intact protein functio... View ClinVar record SCV000664943.5
Ascentage Pharma Group Inc. (United States) Trial sponsor Named in trial inclusion criteriaTrial eligibility criteria : * Has an Eastern Cooperative Oncology Group (ECOG) performance status of 0 to 1 in dose escalation or 0 to 2 in dose expansion * Has a life expectancy of ... View trial NCT05415098
Ascentage Pharma Group Inc. (United States) Trial sponsor Mentioned in trial textTrial free-text mention SMARCB1 View trial NCT05415098

Trial-cited literature (124)

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-609, a Heterobifunctional Degrader of Bromodomain-Containing Protein 9, in Patients with Advanced Synovial Sarcoma or SMARCB1-Deficient Tumors. Clinical cancer research : an official journal of the American Association for Cancer Research 2025 35
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
Study protocol for the Heads-Up trial: a phase II randomized controlled trial investigating head-up tilt sleeping to alleviate orthostatic intolerance in Parkinson's Disease and parkinsonism. BMC neurology 2024 3

Protein variant mentions (11)

Shown in this order: alphabetical by variant.

Protein variant mentions
Variant Distinct papers Year range Sample papers
p.E40X 1 2011 PMID 21809989
p.G11R 1 2015 PMID 25741868
p.G271E 1 2015 PMID 25741868
p.K363E 1 2015 PMID 25741868
p.K363N 2 2014 to 2015 PMID 25741868, PMID 25326635

Literature-extracted relations (17)

Shown in this order: chemicals, then diseases.

Literature-extracted relations
Related entity Kind Source relation label Paper Year
Neoplasms Disease associate A Phase I Study of FHD-609, a Heterobifunctional Degrader of Bromodomain-Containing Protein 9, in Patients with Advanced Synovial Sarcoma or SMARCB1-Deficient Tumors. 2025
Neoplasms Disease associate Molecularly Defined Thoracic Neoplasms. 2024
Sarcoma Disease inhibit The efficacy and safety of vincristine, irinotecan and anlotinib in Epithelioid Sarcoma. 2024
Carcinoma, Renal Cell Disease associate The 2022 World Health Organization Classification of Tumours of the Urinary System and Male Genital Organs-Part A: Renal, Penile, and Testicular Tumours. 2022
Pancreatic Neoplasms Disease associate SWI/SNF complex alterations as a biomarker of immunotherapy efficacy in pancreatic cancer. 2021

Organizations publishing (231)

Shown in this order: most papers first.

Organizations publishing
Organization Type Papers Years
The University of Texas System Academic 13 2009 to 2025
Memorial Sloan Kettering Cancer Center Hospital 12 2015 to 2025
Harris Health System Hospital 7 2013 to 2022
CERCA Institution Government 6 2013 to 2022
Harvard Medical School Academic 6 2004 to 2025

Where SMARCB1 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
  • integumentary system disease
  • measurement
  • nervous system disease
  • phenotype
  • urinary system disease

361 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