Component

Mouse copper transporter Ctr2 / Slc31a2

Mouse copper transporter Ctr2 / Slc31a2. 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.

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. Ctr2 was required for normal formation of the ectodomain-cleaved form of Ctr1 in mice.

    Experimental context and source evidence
    evidence_span
    {"source_cache": "artifacts/copper-research/24167251.abstract.txt", "locator": "Exact primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "7315e9041dddd5510d6efd970560c80316d38120ba1d8eefca10952be8ea0968", "start_char": 0, "end_char": 1212, "text_sha256": "7315e9041dddd5510d6efd970560c80316d38120ba1d8eefca10952be8ea0968"}
    experimental_model
    Ctr2 knockout and Ctr1 processing experiments
    exposure
    Ctr2 deletion
    limitations
    CTR2 regulates truncated CTR1 and intracellular mobilization; it should not simply be treated as a duplicate plasma-membrane CTR1 importer.
    nutrient_topic
    Copper research collection; topical membership is not evidence of a direct dietary effect. · Copper
    organism
    Mouse
    plain_language
    One copper transporter controls the processing of another.
    primary_references
    [copper-p24167251] Ctr2 regulates biogenesis of a cleaved form of mammalian Ctr1 metal transporter lacking the copper- and cisplatin-binding ecto-domain. (2013). https://pubmed.ncbi.nlm.nih.gov/24167251/ DOI: 10.1073/pnas.1311749110
    tissue_or_cell_type
    Tissues and endosomal copper pools

    Copper: transport, cuproenzymes, deficiency, excess and nutrient interactions (2026-09-17) · lines 468–479

    AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Ctr2 knockout and Ctr1 processing experiments · source_derived_draft · unverified_draft

    ### copper-ctr2-ctr1-cleavage Ctr2 was required for normal formation of the ectodomain-cleaved form of Ctr1 in mice. Condition category: normal nutrient_topic: Copper research collection; topical membership is not evidence of a direct dietary effect. plain_language: One copper transporter controls the processing of another. organism: Mouse tissue_or_cell_type: Tissues and endosomal copper pools experimental_model: Ctr2 knockout and Ctr1 processing experiments limitations: CTR2 regulates truncated CTR1 and intracellular mobilization; it should not simply be treated as a duplicate plasma-membrane CTR1 importer. exposure: Ctr2 deletion evidence_span: {"source_cache": "artifacts/copper-research/24167251.abstract.txt", "locator": "Exact primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "7315e9041dddd5510d6efd970560c80316d38120ba1d8eefca10952be8ea0968", "start_char": 0, "end_char": 1212, "text_sha256": "7315e9041dddd5510d6efd970560c80316d38120ba1d8eefca10952be8ea0968"} [copper-p24167251] Ctr2 regulates biogenesis of a cleaved form of mammalian Ctr1 metal transporter lacking the copper- and cisplatin-binding ecto-domain. (2013). https://pubmed.ncbi.nlm.nih.gov/24167251/ DOI: 10.1073/pnas.1311749110
    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