Component

TRPM6 S141L

Disease-associated serine-141-to-leucine TRPM6 variant.

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.

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. TRPM6 S141L disrupted oligomeric assembly and functional TRPM6/TRPM7 complex formation.

    TRPM6 S141L → TRPM6/TRPM7 heteromeric channel complex source_derived_draftungraded
    Experimental context and source evidence
    availability_state
    machinery_impairment Imported condition classification; unverified.
    evidence-system
    Mutant coexpression and channel assembly assays
    experimental_model
    Mutant coexpression and channel assembly assays
    limitations
    A particular variant mechanism; not all TRPM6 variants act by defective trafficking.
    nutrient_topic
    Magnesium research collection; topical membership is not evidence of a direct dietary effect. · Magnesium
    organism
    Human proteins
    plain_language
    This disease-associated substitution damages assembly of the magnesium-entry machinery.
    primary_references
    [chubanov-2004-trpm6-trpm7] Disruption of TRPM6/TRPM7 complex formation by a mutation in the TRPM6 gene causes hypomagnesemia with secondary hypocalcemia. (2004). https://pubmed.ncbi.nlm.nih.gov/14976260/ DOI: 10.1073/pnas.0305252101
    tissue
    HEK293 and Xenopus expression systems
    tissue_or_cell_type
    HEK293 and Xenopus expression systems
    trigger_kind
    machinery_impairment Imported condition classification; unverified.

    Magnesium: cross-nutrient mechanisms and deficiency (2026-09-17) · lines 896–907

    AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Mutant coexpression and channel assembly assays · source_derived_draft · unverified_draft

    ### trpm6-s141l-assembly-defect TRPM6 S141L disrupted oligomeric assembly and functional TRPM6/TRPM7 complex formation. Condition category: machinery_impairment nutrient_topic: Magnesium research collection; topical membership is not evidence of a direct dietary effect. plain_language: This disease-associated substitution damages assembly of the magnesium-entry machinery. organism: Human proteins tissue_or_cell_type: HEK293 and Xenopus expression systems experimental_model: Mutant coexpression and channel assembly assays limitations: A particular variant mechanism; not all TRPM6 variants act by defective trafficking. evidence-system: Mutant coexpression and channel assembly assays tissue: HEK293 and Xenopus expression systems [chubanov-2004-trpm6-trpm7] Disruption of TRPM6/TRPM7 complex formation by a mutation in the TRPM6 gene causes hypomagnesemia with secondary hypocalcemia. (2004). https://pubmed.ncbi.nlm.nih.gov/14976260/ DOI: 10.1073/pnas.0305252101
    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