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Gene

BTBD7

BTBD7 is a gene biomarker in the evidence tier "FDA companion diagnostic". This page lists evidence by type: FDA companion diagnostic assertions (1), Assay-provider ledger (5), Target-disease associations (30), and 3 more evidence types, each linked to its source.

Ensembl ENSG00000011114 UniProt Q9P203 Matched to Ensembl and UniProt
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FDA companion diagnostic assertions FDA companion diagnostic assertions 1 Assay-provider ledger Assay-provider ledger 5 Target-disease associations Target-disease associations 30 Vendor sourcing Vendor sourcing 2 Trial-cited literature Trial-cited literature 5 Organizations publishing Organizations publishing 7 FDA companion diagnostic assertions FDA companion diagnostic assertions 1 Assay-provider ledger Assay-provider ledger 5 Target-disease associations Target-disease associations 30 Vendor sourcing Vendor sourcing 2 Trial-cited literature Trial-cited literature 5 Organizations publishing Organizations publishing 7

Rows recorded per section (log scale)

6 sections measured, none recorded

FDA companion diagnostic

An FDA-cleared or approved companion diagnostic names this biomarker.

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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 papers our biomarker dictionary matched in a year mention BTBD7. The denominator is documents that mention any gene, not every registered document, so improving the matcher moves both halves and never rewrites history. 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.

Publication mentions: plotted from 1990 to 2023, the years our matched corpus covers.

BTBD7 has 5 publication mentions across 5 years. That is too few to read as a trend, so the years are listed instead.

The yearly numbers
BTBD7 per year, by evidence type, the most recent 10 years, newest first; the chart covers 1990 to 2023. The share is of the 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 Publication mentions Share of that year
2023 1 of 11,460 0.01%
2022 0 of 13,598 0.00%
2021 1 of 15,045 0.01%
2020 1 of 14,459 0.01%
2019 0 of 12,159 0.00%
2018 0 of 11,854 0.00%
2017 0 of 11,595 0.00%
2016 0 of 10,983 0.00%
2015 0 of 11,395 0.00%
2014 1 of 10,367 0.01%

FDA companion diagnostic assertions (1)

Shown in this order: most recent decision first.

FDA companion diagnostic assertions
Diagnostic Source biomarker wording Manufacturer Indication Decision date
Idylla CDx MSI Test BTBD7 Biocartis US, Inc. Colorectal Cancer (CRC) 2025-08-15

Assay-provider ledger (5)

Shown in this order: most recent publication first.

Assay-provider ledger
Company Provider class Validation Papers Most recent publication
Biocartis Diagnostic provider Clinical validation 3 September 01, 2025
Agilent Technologies Reagent supplier Clinical validation 1 July 24, 2021
DAKO (Carpinteria, CA, USA) - IHC antibodies and Autostainer Link 48 platform Context dependent Clinical validation 1 July 24, 2021
Diatech Pharmacogenetics Diagnostic provider Clinical validation 1 July 24, 2021
Qiagen (Hilden, Germany) - Mini Amp DNA extraction kit Reagent supplier Clinical validation 1 July 24, 2021

Target-disease associations (30)

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

Target-disease associations
Disease Therapeutic area Source
Hearing loss - familial salivary gland insensitivity to aldosterone genetic, familial or congenital disease Mouse knockout (IMPC)
Salivary Gland Pleomorphic Adenoma gastrointestinal disease Mouse knockout (IMPC)
adrenal cortex carcinoma cancer or benign tumor Literature (Europe PMC)
arterial stiffness measurement measurement GWAS credible sets
body mass index measurement GWAS credible sets

Vendor sourcing (2)

Shown in this order: alphabetical by organization.

Vendor sourcing
Organization Role Tier Evidence Citation
Ambry Genetics (United States) Testing lab / CRO (runs the assay) Clinical-testing interpretation submitted (ClinVar)ClinVar clinical-testing submission The c.2771G>A (p.R924Q) alteration is located in exon 11 (coding exon 10) of the BTBD7 gene. This alteration results from a G to A substitution at nucleotide... View ClinVar record SCV003543093.3
Not resolved to an organization Diagnostics manufacturer FDA-authorized companion diagnosticFDA companion diagnostic authorization Microsatellite instability-High (MSI-H) View FDA device record

Trial-cited literature (5)

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

Trial-cited literature
Publication Journal Year Citations
Web-Based Asynchronous Tool to Facilitate Communication Between Primary Care Providers and Cancer Specialists: Pragmatic Randomized Controlled Trial. Journal of medical Internet research 2023 7
Tracking tDCS induced grey matter changes in episodic migraine: a randomized controlled trial. The journal of headache and pain 2021 8
Automatic mandibular canal detection using a deep convolutional neural network. Scientific reports 2020 85
Three-dimensional organotypic culture: experimental models of mammalian biology and disease. Nature reviews. Molecular cell biology 2014 549
Long-term (6 and 12 months) follow-up of two prospective, randomized, controlled phase III trials of photodynamic therapy with BF-200 ALA and methyl aminolaevulinate for the treatment of actinic keratosis. The British journal of dermatology 2013 79

Organizations publishing (7)

Shown in this order: most papers first.

Organizations publishing
Organization Type Papers Years
Johns Hopkins University Academic 1 2014
McMaster University Academic 1 2023
Pusan National University Academic 1 2020
Seoul National University Academic 1 2020
University Hospital Zurich Hospital 1 2021

Where BTBD7 appears

  • cancer or benign tumor
  • cardiovascular disease
  • gastrointestinal disease
  • genetic, familial or congenital disease
  • measurement
  • nutritional or metabolic disease
  • phenotype

30 diseases touched.

Not on this page

Checked, with nothing recorded for this biomarker: fda biomarker qualification projects, actionable biomarkers, trial mentions, protein variant mentions, human sample screening reference, and literature-extracted relations.

Browse all biomarker evidence pages