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Gene

IGF2

IGF2 is a gene biomarker in the evidence tier "Cancer actionable (CGI)". This page lists evidence by type: Assay-provider ledger (50), Actionable biomarkers (1), Trial mentions (12), and 5 more evidence types, each linked to its source.

Ensembl ENSG00000167244 UniProt P01344 Matched to Ensembl and UniProt
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Assay-provider ledger Assay-provider ledger 50 Actionable biomarkers Actionable biomarkers 1 Trial mentions Trial mentions 12 Target-disease associations Target-disease associations 387 Vendor sourcing Vendor sourcing 38 Trial-cited literature Trial-cited literature 470 Literature-extracted relations Literature-extracted relations 79 Organizations publishing Organizations publishing 384 Assay-provider ledger Assay-provider ledger 50 Actionable biomarkers Actionable biomarkers 1 Trial mentions Trial mentions 12 Target-disease associations Target-disease associations 387 Vendor sourcing Vendor sourcing 38 Trial-cited literature Trial-cited literature 470 Literature-extracted relations Literature-extracted relations 79 Organizations publishing Organizations publishing 384

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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Evidence over time

Share of that year: what fraction of the trials and papers our biomarker dictionary matched in a year mention IGF2. 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. Not plotted: 1 dated before 1990 and 4 at the structurally incomplete recent edge.

The yearly numbers
IGF2 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 1 of 8,738 0.01% 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% 17 of 11,460 0.15%
2022 0 of 8,285 0.00% 24 of 13,598 0.18%
2021 1 of 8,692 0.01% 35 of 15,045 0.23%
2020 1 of 7,640 0.01% 30 of 14,459 0.21%
2019 0 of 7,300 0.00% 28 of 12,159 0.23%
2018 0 of 6,927 0.00% 23 of 11,854 0.19%
2017 0 of 6,558 0.00% 28 of 11,595 0.24%

Assay-provider ledger (50)

Shown in this order: most recent publication first.

Assay-provider ledger
Company Provider class Validation Papers Most recent publication
Canhelp Genomics Diagnostic provider Clinical validation 1 December 01, 2024
Cepheid Diagnostic provider Clinical validation 1 March 01, 2018
KAPA Biosystems Reagent supplier Clinical validation 1 February 27, 2018
NanoDrop Technologies Reagent supplier Clinical validation 1 February 27, 2018
ROCHE Context dependent Clinical validation 1 February 27, 2018

Actionable biomarkers (1)

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

Actionable biomarkers
Alteration Drug Response Disease Source
IGF2 amplification Egfr Mab Inhibitors responsive colorectal adenocarcinoma Cancer Genome Interpreter

Trial mentions (12)

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

Trial mentions
Trial Source
NCT03576963 Trial eligibility (AACT)
NCT07497477 Trial eligibility (AACT)
NCT02028221 Trial outcomes (AACT)
NCT01721577 Trial outcomes (AACT)
NCT01041027 Trial outcomes (AACT)

Target-disease associations (387)

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

Target-disease associations
Disease Therapeutic area Source
Abdominal obesity nutritional or metabolic disease Literature (Europe PMC)
Abnormal sperm morphology phenotype Literature (Europe PMC)
Abnormality of the skeletal system phenotype GWAS credible sets
Alzheimer disease nervous system disease Literature (Europe PMC)
Anxiety phenotype Literature (Europe PMC)

Vendor sourcing (38)

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 v4.1.0 dataset. Predicted Consequence/Location: Missense variant In silico tool predictions suggest damaging effect... View ClinVar record SCV007610919.1
Albert Einstein College of Medicine Trial sponsor Mentioned in trial textTrial free-text mention IGF2 View trial NCT01041027
Ambry Genetics (United States) Testing lab / CRO (runs the assay) Clinical-testing interpretation submitted (ClinVar)ClinVar clinical-testing submission The c.100G>C (p.G34R) alteration is located in exon 2 (coding exon 1) of the IGF2 gene. This alteration results from a G to C substitution at nucleotide posi... View ClinVar record SCV003549985.2
Assistance Publique – Hôpitaux de Paris Trial sponsor Named in trial inclusion criteriaTrial eligibility criteria : 1. "Negative control" population: subjects who have undergone genetic exploration and: * Having had a study of normal methylation of the 11p15 region ... View trial NCT07497477
Assistance Publique – Hôpitaux de Paris Trial sponsor Mentioned in trial textTrial free-text mention IGF2 View trial NCT07497477

Trial-cited literature (470)

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

Trial-cited literature
Publication Journal Year Citations
Reciprocal regulation of hMENA and TGF-β signaling in cancer-associated fibroblasts promotes EMT, immunosuppression, poor prognosis, and ICT resistance in NSCLC. Journal for immunotherapy of cancer 2026 1
Cardiometabolic function in Offspring, Mother and Placenta after Assisted Reproductive Technology (COMPART): a prospective cohort study. BMJ open 2025 0
Targeting IGF2 to reprogram the tumor microenvironment for enhanced viro-immunotherapy. Neuro-oncology 2024 23
Efficacy of GV1001 with gemcitabine/capecitabine in previously untreated patients with advanced pancreatic ductal adenocarcinoma having high serum eotaxin levels (KG4/2015): an open-label, randomised, Phase 3 trial. British journal of cancer 2024 23
c-MYC mediates the crosstalk between breast cancer cells and tumor microenvironment. Cell communication and signaling : CCS 2023 148

Literature-extracted relations (79)

Shown in this order: chemicals, then diseases.

Literature-extracted relations
Related entity Kind Source relation label Paper Year
Anhydrous glucose Chemical positive_correlate Preptin: A New Bone Metabolic Parameter? 2023
Anhydrous glucose Chemical positive_correlate Maternal serum preptin levels in the pathogenesis and diagnosis of Gestational diabetes mellitus. 2023
(R,S)-ketamine (Pilot I) Chemical positive_correlate The Mechanisms Behind Rapid Antidepressant Effects of Ketamine: A Systematic Review With a Focus on Molecular Neuroplasticity. 2022
Anhydrous glucose Chemical positive_correlate Cytokines and Hormones That Contribute to the Positive Association between Fat and Bone. 2014
Anhydrous glucose Chemical associate Three new players in energy regulation: preptin, adropin and irisin. 2014

Organizations publishing (384)

Shown in this order: most papers first.

Organizations publishing
Organization Type Papers Years
Government of the United States of America Government 24 2000 to 2024
Harvard Medical School Academic 13 2011 to 2022
Mass General Brigham Hospital 12 2011 to 2023
The University of Texas System Academic 10 2009 to 2024
Dana-Farber Cancer Institute Other 9 2005 to 2022

Where IGF2 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
  • measurement
  • musculoskeletal or connective tissue disease
  • nervous system disease
  • nutritional or metabolic disease
  • phenotype
  • pregnancy or perinatal disease
  • reproductive system or breast disease
  • respiratory or thoracic disease
  • 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, protein variant mentions, and human sample screening reference.

Browse all biomarker evidence pages