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Gene

SLC29A1

SLC29A1 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 (8), and 5 more evidence types, each linked to its source.

Ensembl ENSG00000112759 UniProt Q99808 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 8 Target-disease associations Target-disease associations 117 Vendor sourcing Vendor sourcing 28 Trial-cited literature Trial-cited literature 72 Literature-extracted relations Literature-extracted relations 23 Organizations publishing Organizations publishing 89 Assay-provider ledger Assay-provider ledger 3 Actionable biomarkers Actionable biomarkers 1 Trial mentions Trial mentions 8 Target-disease associations Target-disease associations 117 Vendor sourcing Vendor sourcing 28 Trial-cited literature Trial-cited literature 72 Literature-extracted relations Literature-extracted relations 23 Organizations publishing Organizations publishing 89

Rows recorded per section (log scale)

4 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 SLC29A1. 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.

SLC29A1 has 8 trial mentions across 7 years. That is too few to read as a trend, so the years are listed instead.

The yearly numbers
SLC29A1 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 0 of 8,738 0.00% not measured
2025 0 of 8,875 0.00% not measured
2024 0 of 8,597 0.00% not measured
2023 0 of 8,275 0.00% 4 of 11,460 0.03%
2022 0 of 8,285 0.00% 3 of 13,598 0.02%
2021 0 of 8,692 0.00% 4 of 15,045 0.03%
2020 0 of 7,640 0.00% 6 of 14,459 0.04%
2019 0 of 7,300 0.00% 10 of 12,159 0.08%
2018 0 of 6,927 0.00% 8 of 11,854 0.07%
2017 0 of 6,558 0.00% 10 of 11,595 0.09%

Assay-provider ledger (3)

Shown in this order: most recent publication first.

Assay-provider ledger
Company Provider class Validation Papers Most recent publication
Ventana Medical Systems Unclassified Clinical validation 1 August 01, 2015
Clovis Oncology Inc. Pharma or other Clinical validation 1 July 01, 2014
Trillium Diagnostics Diagnostic provider Analytical validation 1 Date unknown

Actionable biomarkers (1)

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

Actionable biomarkers
Alteration Drug Response Disease Source
SLC29A1 oncogenic mutation GEMCITABINE responsive No disease recorded Cancer Genome Interpreter

Trial mentions (8)

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

Trial mentions
Trial Source
NCT01035502 Trial eligibility (AACT)
NCT01586611 Trial eligibility (AACT)
NCT01411072 Trial eligibility (AACT)
NCT01233375 Trial eligibility (AACT)
NCT01124786 Trial outcomes (AACT)

Target-disease associations (117)

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

Target-disease associations
Disease Therapeutic area Source
Acute Leukemia cancer or benign tumor Literature (Europe PMC)
Ampulla of Vater Carcinoma cancer or benign tumor Literature (Europe PMC)
COVID-19 infectious disease Clinical precedence
COVID-19 infectious disease Literature (Europe PMC)
Calvarial doughnut lesions - bone fragility genetic, familial or congenital disease Mouse knockout (IMPC)

Vendor sourcing (28)

Shown in this order: alphabetical by organization.

Vendor sourcing
Organization Role Tier Evidence Citation
AHS Cancer Control Alberta Trial sponsor Named in trial inclusion criteriaTrial eligibility criteria : * Histologically documented pancreatic adenocarcinoma not previously treated with systemic therapy. * Complete macroscopic and microscopic (R0) resection ... View trial NCT01411072
AHS Cancer Control Alberta Trial sponsor Named in trial inclusion criteriaTrial eligibility criteria : * Histologically documented metastatic pancreatic adenocarcinoma not previously treated with palliative systemic therapy * Metastatic disease based on the... View trial NCT01586611
AHS Cancer Control Alberta Trial sponsor Primary endpoint in a Phase 3 trialTrial endpoint The difference Progression Free Survival (PFS) between Gemcitabine and FOLFOX treated patients in hENT1 high and hENT1 low pancreatic adenocarcinoma. View trial NCT01586611
AHS Cancer Control Alberta Trial sponsor Mentioned in trial textTrial free-text mention hENT1 View trial NCT01411072
AHS Cancer Control Alberta Trial sponsor Mentioned in trial textTrial free-text mention hENT1 View trial NCT01586611

Trial-cited literature (72)

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

Trial-cited literature
Publication Journal Year Citations
The Safety and Antiaging Effects of Nicotinamide Mononucleotide in Human Clinical Trials: an Update. Advances in nutrition (Bethesda, Md.) 2023 81
Molecular targeting of the UDP-glucuronosyltransferase enzymes in high-eukaryotic translation initiation factor 4E refractory/relapsed acute myeloid leukemia patients: a randomized phase II trial of vismodegib, ribavirin with or without decitabine. Haematologica 2023 15
Erythrocyte type 1 equilibrative nucleoside transporter expression in sickle cell disease and sickle cell trait. British journal of haematology 2023 2
A novel approach to overcome drug resistance in acute myeloid leukemia. Haematologica 2023 1
Cancer biology and molecular genetics of A<sub>3</sub> adenosine receptor. Oncogene 2022 76

Literature-extracted relations (23)

Shown in this order: chemicals, then diseases.

Literature-extracted relations
Related entity Kind Source relation label Paper Year
Adenosine Chemical associate Erythrocyte type 1 equilibrative nucleoside transporter expression in sickle cell disease and sickle cell trait. 2023
Adenosine Chemical associate Ticagrelor and preconditioning in patients with stable coronary artery disease (TAPER-S): a randomized pilot clinical trial. 2020
Ticagrelor Chemical negative_correlate Ticagrelor and preconditioning in patients with stable coronary artery disease (TAPER-S): a randomized pilot clinical trial. 2020
Cladribine Chemical associate The Clinical Pharmacology of Cladribine Tablets for the Treatment of Relapsing Multiple Sclerosis. 2019
Dipyridamole Chemical negative_correlate Treatment of restless legs syndrome/Willis-Ekbom disease with the non-selective ENT1/ENT2 inhibitor dipyridamole: testing the adenosine hypothesis. 2018

Organizations publishing (89)

Shown in this order: most papers first.

Organizations publishing
Organization Type Papers Years
Government of the United States of America Government 2 2017 to 2018
Mayo Clinic Hospital 2 2017 to 2020
Memorial Sloan Kettering Cancer Center Hospital 2 2018 to 2022
Newcastle University Academic 2 2016 to 2017
Northwestern University Academic 2 2020 to 2023

Where SLC29A1 appears

  • cancer or benign tumor
  • cardiovascular disease
  • endocrine system disease
  • genetic, familial or congenital disease
  • hematologic disease
  • immune system disease
  • infectious disease
  • injury, poisoning or other complication
  • measurement
  • nervous system disease
  • nutritional or metabolic disease
  • phenotype
  • urinary system disease

114 diseases touched.

Not on this page

Checked, with nothing recorded for this biomarker: fda companion diagnostic assertions, fda biomarker qualification projects, protein variant mentions, and human sample screening reference.

Browse all biomarker evidence pages