Component

CYP2A6 variant alleles in the 1995 coumarin phenotyping study; original nomenclature retained

CYP2A6 variant alleles in the 1995 coumarin phenotyping study; original nomenclature retained. Species, exposure and limitations are retained in each linked claim.

1 recorded relationships. Experimental role, claim status and evidence remain attached to each record.

How nutrients influence it

Every nutrient with a recorded effect on this component, credited to the nutrient that acted rather than the chapter that recorded it. Open a nutrient to see the findings and the conditions they were measured under.

How nutrients reach it in more than one step

Chains of two or more recorded steps that end here, grouped by the nutrient they start from. Each step is a separate finding, so a chain is a route a mechanism could take, not proof that it does.

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What it does

Every recorded relationship this component is part of, grouped by its role. Plain wording comes first; the technical statement follows.

Recorded relationships

What it acts on

  1. CYP2A6 variant alleles were identified in individuals with poor coumarin metabolism, including a single-amino-acid inactivating variant.

    Experimental context and source evidence
    availability_state
    machinery_impairment Imported condition classification; unverified.
    evidence_span
    {"source_cache": "artifacts/coumarin-research/7668294.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "aeb377e6bbda1a552066c5d1caf1bf558753096627b863835637a0f2f942b3b1", "start_char": 0, "end_char": 1316, "text_sha256": "aeb377e6bbda1a552066c5d1caf1bf558753096627b863835637a0f2f942b3b1"}
    experimental_model
    CYP2A gene sequencing and coumarin metabolic phenotyping
    exposure
    Original CYP2A6v1/v2 nomenclature; poor-metabolizer individuals
    limitations
    Historical variant labels retained; no automatic mapping to modern star alleles and no demonstrated prediction of liver injury.
    nutrient_topic
    Coumarin research collection; topical membership is not evidence of a direct dietary effect. · Coumarin
    organism
    Human
    plain_language
    Inherited enzyme differences can change how coumarin is processed.
    primary_references
    [coumarin-p7668294] A genetic polymorphism in coumarin 7-hydroxylation: sequence of the human CYP2A genes and identification of variant CYP2A6 alleles. (1995). https://pubmed.ncbi.nlm.nih.gov/7668294/
    tissue_or_cell_type
    Genomic DNA and whole-body probe metabolism
    trigger_kind
    machinery_impairment Imported condition classification; unverified.

    Coumarin: metabolism, signaling and nutrient connections (2026-09-17) · lines 631–642

    AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · CYP2A gene sequencing and coumarin metabolic phenotyping · source_derived_draft · unverified_draft

    ### coumarin-genetic-variation CYP2A6 variant alleles were identified in individuals with poor coumarin metabolism, including a single-amino-acid inactivating variant. Condition category: machinery_impairment nutrient_topic: Coumarin research collection; topical membership is not evidence of a direct dietary effect. plain_language: Inherited enzyme differences can change how coumarin is processed. organism: Human tissue_or_cell_type: Genomic DNA and whole-body probe metabolism experimental_model: CYP2A gene sequencing and coumarin metabolic phenotyping limitations: Historical variant labels retained; no automatic mapping to modern star alleles and no demonstrated prediction of liver injury. exposure: Original CYP2A6v1/v2 nomenclature; poor-metabolizer individuals evidence_span: {"source_cache": "artifacts/coumarin-research/7668294.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "aeb377e6bbda1a552066c5d1caf1bf558753096627b863835637a0f2f942b3b1", "start_char": 0, "end_char": 1316, "text_sha256": "aeb377e6bbda1a552066c5d1caf1bf558753096627b863835637a0f2f942b3b1"} [coumarin-p7668294] A genetic polymorphism in coumarin 7-hydroxylation: sequence of the human CYP2A genes and identification of variant CYP2A6 alleles. (1995). https://pubmed.ncbi.nlm.nih.gov/7668294/
    Complete structured claim and evidence

In the sources

Preserved passages that mention this component, quoted exactly. Open one to read it in context.

    This is a research prototype built from draft material. It is not medical advice, and its statements still await verification against the original studies.

    Evidence, AI assistance and curation standards