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Gene

CDKN2C

CDKN2C is a gene biomarker in the evidence tier "Cancer actionable (CGI)". This page lists evidence by type: Assay-provider ledger (3), Actionable biomarkers (4), Trial mentions (1), and 5 more evidence types, each linked to its source.

Ensembl ENSG00000123080 UniProt P42773 Matched to Ensembl and UniProt
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Assay-provider ledger Assay-provider ledger 3 Actionable biomarkers Actionable biomarkers 4 Trial mentions Trial mentions 1 Target-disease associations Target-disease associations 442 Vendor sourcing Vendor sourcing 6 Trial-cited literature Trial-cited literature 61 Literature-extracted relations Literature-extracted relations 1 Organizations publishing Organizations publishing 97 Assay-provider ledger Assay-provider ledger 3 Actionable biomarkers Actionable biomarkers 4 Trial mentions Trial mentions 1 Target-disease associations Target-disease associations 442 Vendor sourcing Vendor sourcing 6 Trial-cited literature Trial-cited literature 61 Literature-extracted relations Literature-extracted relations 1 Organizations publishing Organizations publishing 97

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 CDKN2C. 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.

CDKN2C has 1 trial mention across 1 year. That is too few to read as a trend, so the years are listed instead.

The yearly numbers
CDKN2C 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 1 of 8,597 0.01% not measured
2023 0 of 8,275 0.00% 3 of 11,460 0.03%
2022 0 of 8,285 0.00% 4 of 13,598 0.03%
2021 0 of 8,692 0.00% 7 of 15,045 0.05%
2020 0 of 7,640 0.00% 3 of 14,459 0.02%
2019 0 of 7,300 0.00% 3 of 12,159 0.02%
2018 0 of 6,927 0.00% 3 of 11,854 0.03%
2017 0 of 6,558 0.00% 9 of 11,595 0.08%

Assay-provider ledger (3)

Shown in this order: most recent publication first.

Assay-provider ledger
Company Provider class Validation Papers Most recent publication
Kumei Biotechnology Co. Reagent supplier Clinical validationAnalytical validation 1 October 01, 2024
QIAGEN Reagent supplier Clinical validationAnalytical validation 1 October 01, 2024
TransGen Biotech Reagent supplier Clinical validationAnalytical validation 1 October 01, 2024

Actionable biomarkers (4)

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

Actionable biomarkers
Alteration Drug Response Disease Source
CDKN2C deletion Cdk2 Inhibitors response-associated glioma Cancer Genome Interpreter
CDKN2C oncogenic mutation Cdk2 Inhibitors response-associated glioma Cancer Genome Interpreter
CDKN2C deletion Cdk2 Inhibitors response-associated No disease recorded Cancer Genome Interpreter
CDKN2C oncogenic mutation Cdk2 Inhibitors response-associated No disease recorded Cancer Genome Interpreter

Trial mentions (1)

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

Trial mentions
Trial Source
NCT05843253 Trial eligibility (AACT)

Target-disease associations (442)

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

Target-disease associations
Disease Therapeutic area Source
46,XY partial gonadal dysgenesis endocrine system disease Mouse knockout (IMPC)
ATP measurement measurement GWAS credible sets
Ataxia-telangiectasia disorder of visual system Mouse knockout (IMPC)
Atypical Meningioma cancer or benign tumor Cancer Gene Census
Autoimmune lymphoproliferative syndrome with recurrent viral infections genetic, familial or congenital disease Mouse knockout (IMPC)

Vendor sourcing (6)

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.408G>C (p.K136N) alteration is located in exon 3 (coding exon 2) of the CDKN2C gene. This alteration results from a G to C substitution at nucleotide p... View ClinVar record SCV003592829.2
Memorial Sloan Kettering Cancer Center Testing lab / CRO (runs the assay) Clinical-testing interpretation submitted without stated criteria (ClinVar)ClinVar clinical-testing submission No supporting text recorded; see the citation. View ClinVar record SCV001132092.1
Nationwide Children's Hospital Trial sponsor Named in trial inclusion criteriaTrial eligibility criteria for assignment to TarGeT-A, for all strata: 2.1) Presence of at least one relevant actionable somatic alteration, detailed here: * Pathogenic alterations p... View trial NCT05843253
Nationwide Children's Hospital Trial sponsor Mentioned in trial textTrial free-text mention CDKN2C View trial NCT05843253
Novartis Ag Trial collaborator Named in trial inclusion criteriaTrial eligibility criteria for assignment to TarGeT-A, for all strata: 2.1) Presence of at least one relevant actionable somatic alteration, detailed here: * Pathogenic alterations p... View trial NCT05843253

Trial-cited literature (61)

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

Trial-cited literature
Publication Journal Year Citations
A biobank of pediatric patient-derived-xenograft models in cancer precision medicine trial MAPPYACTS for relapsed and refractory tumors. Communications biology 2023 24
Single-cell profiling of multiple myeloma reveals molecular response to FGFR3 inhibitor despite clinical progression. Cold Spring Harbor molecular case studies 2023 6
Activity of pemetrexed in pre-clinical chordoma models and humans. Scientific reports 2023 4
Perspectives on the Risk-Stratified Treatment of Multiple Myeloma. Blood cancer discovery 2022 38
MEN4, the MEN1 Mimicker: A Case Series of three Phenotypically Heterogenous Patients With Unique CDKN1B Mutations. The Journal of clinical endocrinology and metabolism 2022 27

Literature-extracted relations (1)

Shown in this order: chemicals, then diseases.

Literature-extracted relations
Related entity Kind Source relation label Paper Year
Neoplasms Disease associate Pooled ctDNA analysis of MONALEESA phase III advanced breast cancer trials. 2023

Organizations publishing (97)

Shown in this order: most papers first.

Organizations publishing
Organization Type Papers Years
Dana-Farber Cancer Institute Other 4 2014 to 2022
Government of the United States of America Government 4 2003 to 2022
Memorial Sloan Kettering Cancer Center Hospital 4 2012 to 2022
Harvard Medical School Academic 3 2014 to 2022
Mayo Clinic Hospital 3 2017 to 2022

Where CDKN2C appears

  • biological_process
  • cancer or benign tumor
  • cardiovascular disease
  • disorder of visual system
  • endocrine system disease
  • gastrointestinal disease
  • genetic, familial or congenital disease
  • immune system disease
  • infectious disease
  • integumentary system disease
  • measurement
  • nervous system disease
  • nutritional or metabolic disease
  • phenotype
  • reproductive system or breast disease
  • respiratory or thoracic disease
  • urinary system disease

409 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