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Gene

PRKCH

PRKCH is a gene biomarker in the evidence tier "Cancer actionable (CGI)". This page lists evidence by type: Assay-provider ledger (5), Actionable biomarkers (2), Target-disease associations (292), and 4 more evidence types, each linked to its source.

Ensembl ENSG00000027075 UniProt P24723 Matched to Ensembl and UniProt
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Assay-provider ledger Assay-provider ledger 5 Actionable biomarkers Actionable biomarkers 2 Target-disease associations Target-disease associations 292 Vendor sourcing Vendor sourcing 3 Trial-cited literature Trial-cited literature 7 Protein variant mentions Protein variant mentions 2 Organizations publishing Organizations publishing 15 Assay-provider ledger Assay-provider ledger 5 Actionable biomarkers Actionable biomarkers 2 Target-disease associations Target-disease associations 292 Vendor sourcing Vendor sourcing 3 Trial-cited literature Trial-cited literature 7 Protein variant mentions Protein variant mentions 2 Organizations publishing Organizations publishing 15

Rows recorded per section (log scale)

5 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 papers our biomarker dictionary matched in a year mention PRKCH. 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.

PRKCH has 7 publication mentions across 6 years. That is too few to read as a trend, so the years are listed instead.

The yearly numbers
PRKCH 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 0 of 11,460 0.00%
2022 0 of 13,598 0.00%
2021 0 of 15,045 0.00%
2020 1 of 14,459 0.01%
2019 0 of 12,159 0.00%
2018 1 of 11,854 0.01%
2017 0 of 11,595 0.00%
2016 1 of 10,983 0.01%
2015 0 of 11,395 0.00%
2014 1 of 10,367 0.01%

Assay-provider ledger (5)

Shown in this order: most recent publication first.

Assay-provider ledger
Company Provider class Validation Papers Most recent publication
NanoString Technologies Unclassified Clinical validation 1 June 18, 2019
Agilent Technologies Reagent supplier Clinical validationAnalytical validation 1 July 25, 2017
Fluidigm Reagent supplier Clinical validationAnalytical validation 1 July 25, 2017
Invitrogen Reagent supplier Clinical validationAnalytical validation 1 July 25, 2017
QIAGEN Reagent supplier Clinical validationAnalytical validation 1 July 25, 2017

Actionable biomarkers (2)

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

Actionable biomarkers
Alteration Drug Response Disease Source
PRKCH amplification + ABL1-BCR fusion Imatinib response-associated chronic myelogenous leukemia Cancer Genome Interpreter
PRKCH amplification + ABL1-BCR fusion Trametinib response-associated chronic myelogenous leukemia Cancer Genome Interpreter

Target-disease associations (292)

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

Target-disease associations
Disease Therapeutic area Source
22q11.2 deletion syndrome cardiovascular disease Mouse knockout (IMPC)
Aicardi-Goutieres syndrome 2 genetic, familial or congenital disease Mouse knockout (IMPC)
Aicardi-Goutières syndrome genetic, familial or congenital disease Mouse knockout (IMPC)
Alymphoid cystic thymic dysgenesis immune system disease Mouse knockout (IMPC)
Alzheimer disease nervous system disease Literature (Europe PMC)

Vendor sourcing (3)

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.445C>T (p.R149W) alteration is located in exon 3 (coding exon 3) of the PRKCH gene. This alteration results from a C to T substitution at nucleotide po... View ClinVar record SCV003526474.3
Johns Hopkins University 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 SCV001430656.1
Labcorp Holdings Inc. 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 SCV001030402.1

Trial-cited literature (7)

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

Trial-cited literature
Publication Journal Year Citations
The Role of Adaptogens in Prophylaxis and Treatment of Viral Respiratory Infections. Pharmaceuticals (Basel, Switzerland) 2020 33
Replicable and Coupled Changes in Innate and Adaptive Immune Gene Expression in Two Case-Control Studies of Blood Microarrays in Major Depressive Disorder. Biological psychiatry 2018 193
Association and prognostic significance of BRCA1/2-mutation status with neoantigen load, number of tumor-infiltrating lymphocytes and expression of PD-1/PD-L1 in high grade serous ovarian cancer. Oncotarget 2016 509
Transcriptome profiling and pathway analysis of genes expressed differentially in participants with or without a positive response to topiramate treatment for methamphetamine addiction. BMC medical genomics 2014 18
Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score. Molecular medicine (Cambridge, Mass.) 2010 108

Protein variant mentions (2)

Shown in this order: alphabetical by variant.

Protein variant mentions
Variant Distinct papers Year range Sample papers
p.G55A 1 2015 PMID 25741868
p.V374I 1 2010 PMID 20852671

Organizations publishing (15)

Shown in this order: most papers first.

Organizations publishing
Organization Type Papers Years
Beth Israel Deaconess Medical Center Hospital 1 2001
Dana-Farber Cancer Institute Other 1 2016
Duke University Academic 1 2010
Harvard Medical School Academic 1 2016
Mass General Brigham Hospital 1 2016

Where PRKCH 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
  • integumentary system disease
  • measurement
  • medical procedure
  • musculoskeletal or connective tissue disease
  • nervous system disease
  • nutritional or metabolic disease
  • phenotype
  • respiratory or thoracic disease

286 diseases touched.

Not on this page

Checked, with nothing recorded for this biomarker: fda companion diagnostic assertions, fda biomarker qualification projects, trial mentions, human sample screening reference, and literature-extracted relations.

Browse all biomarker evidence pages