Component

TXNRD3

Independent protein record for Thioredoxin glutathione reductase.

2 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.

Tracing routes…

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. Male Txnrd3-knockout mice showed impaired reproductive performance and reduced fertilization in the reported assays.

    TXNRD3 → Male fertility source_derived_draftliterature_reviewed:direct_experimental
    Experimental context and source evidence
    experimental_model
    Txnrd3-knockout mice, sperm thiol assays and in-vitro fertilization.
    limitations
    This experiment-specific relationship does not establish a human dietary-deficiency threshold or supplementation benefit.
    organism
    Mouse

    Selenium: literature corrections and mechanism additions · lines 987–996

    Metabolic Ledger literature curation, 17 September 2026; primary papers linked individually · supports · Txnrd3-knockout mice, sperm thiol assays and in-vitro fertilization. · secondary_verified · secondary_verified

    ## txnrd3-mouse-fertility Removing TXNRD3 impaired fertility in the studied mice. Male Txnrd3-knockout mice showed impaired reproductive performance and reduced fertilization in the reported assays. Experimental model: Txnrd3-knockout mice, sperm thiol assays and in-vitro fertilization. Organism: Mouse Limitations: This experiment-specific relationship does not establish a human dietary-deficiency threshold or supplementation benefit. Primary reference: [Selenoprotein TXNRD3 supports male fertility via the redox regulation of spermatogenesis](https://pmc.ncbi.nlm.nih.gov/articles/PMC9352919/)
    Complete structured claim and evidence
  2. Txnrd3 deletion in mice altered sperm protein thiol status, supporting a role for TXNRD3 in sperm redox remodeling.

    TXNRD3 → Sperm protein thiol homeostasis source_derived_draftliterature_reviewed:supported_interpretation
    Experimental context and source evidence
    experimental_model
    Txnrd3-knockout mice, sperm thiol assays and in-vitro fertilization.
    limitations
    This experiment-specific relationship does not establish a human dietary-deficiency threshold or supplementation benefit.
    organism
    Mouse

    Selenium: literature corrections and mechanism additions · lines 976–985

    Metabolic Ledger literature curation, 17 September 2026; primary papers linked individually · supports · Txnrd3-knockout mice, sperm thiol assays and in-vitro fertilization. · secondary_verified · secondary_verified

    ## txnrd3-sperm-thiol-control TXNRD3 helps manage protein sulfur bonds as sperm mature. Txnrd3 deletion in mice altered sperm protein thiol status, supporting a role for TXNRD3 in sperm redox remodeling. Experimental model: Txnrd3-knockout mice, sperm thiol assays and in-vitro fertilization. Organism: Mouse Limitations: This experiment-specific relationship does not establish a human dietary-deficiency threshold or supplementation benefit. Primary reference: [Selenoprotein TXNRD3 supports male fertility via the redox regulation of spermatogenesis](https://pmc.ncbi.nlm.nih.gov/articles/PMC9352919/)
    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