Component
Mouse heme transporter HRG1 / Slc48a1
Mouse heme transporter HRG1 / Slc48a1. Species, exposure and limitations are retained in each linked claim.
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.
Other things that act on it
Enzymes, hormones, genes, and other components with a recorded effect. These are not nutrients, so they do not count toward the arrows above. Each finding names the chapter that recorded it.
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.
What it acts on
Hrg1 depletion attenuated heme transport from macrophage phagolysosomes.
Experimental context and source evidence
- availability_state
- machinery_impairment Imported condition classification; unverified.
- evidence_span
- {"source_cache": "artifacts/iron-research/23395172.abstract.txt", "locator": "Exact primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "9ffc7159cfb418fed987d6f3f9e34829861a8f4ede0fe564a2714ef0bc96968b", "start_char": 0, "end_char": 1074, "text_sha256": "9ffc7159cfb418fed987d6f3f9e34829861a8f4ede0fe564a2714ef0bc96968b"}
- experimental_model
- Macrophage depletion, localization and human variant assays
- exposure
- Hrg1 depletion and missense variants
- limitations
- Recycling pathway experiment; no estimate of dietary iron requirements is derived.
- nutrient_topic
- Iron research collection; topical membership is not evidence of a direct dietary effect. · Iron
- organism
- Mouse macrophages and human HRG1 variants
- plain_language
- A blocked recycling step can trap useful material inside a cellular compartment.
- primary_references
- [iron-p23395172] HRG1 is essential for heme transport from the phagolysosome of macrophages during erythrophagocytosis. (2013). https://pubmed.ncbi.nlm.nih.gov/23395172/ DOI: 10.1016/j.cmet.2013.01.005
- tissue_or_cell_type
- Phagolysosomes during erythrophagocytosis
- trigger_kind
- machinery_impairment Imported condition classification; unverified.
Iron: absorption, trafficking, iron-dependent enzymes and nutrient interactions (2026-09-17) · lines 563–574
AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Macrophage depletion, localization and human variant assays · source_derived_draft · unverified_draft
### iron-hrg1-loss Hrg1 depletion attenuated heme transport from macrophage phagolysosomes. Condition category: machinery_impairment nutrient_topic: Iron research collection; topical membership is not evidence of a direct dietary effect. plain_language: A blocked recycling step can trap useful material inside a cellular compartment. organism: Mouse macrophages and human HRG1 variants tissue_or_cell_type: Phagolysosomes during erythrophagocytosis experimental_model: Macrophage depletion, localization and human variant assays limitations: Recycling pathway experiment; no estimate of dietary iron requirements is derived. exposure: Hrg1 depletion and missense variants evidence_span: {"source_cache": "artifacts/iron-research/23395172.abstract.txt", "locator": "Exact primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "9ffc7159cfb418fed987d6f3f9e34829861a8f4ede0fe564a2714ef0bc96968b", "start_char": 0, "end_char": 1074, "text_sha256": "9ffc7159cfb418fed987d6f3f9e34829861a8f4ede0fe564a2714ef0bc96968b"} [iron-p23395172] HRG1 is essential for heme transport from the phagolysosome of macrophages during erythrophagocytosis. (2013). https://pubmed.ncbi.nlm.nih.gov/23395172/ DOI: 10.1016/j.cmet.2013.01.005
Complete structured claim and evidenceHrg1 localized to phagolysosomal membranes during erythrophagocytosis and transported heme toward the macrophage cytoplasm.
Experimental context and source evidence
- evidence_span
- {"source_cache": "artifacts/iron-research/23395172.abstract.txt", "locator": "Exact primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "9ffc7159cfb418fed987d6f3f9e34829861a8f4ede0fe564a2714ef0bc96968b", "start_char": 0, "end_char": 1074, "text_sha256": "9ffc7159cfb418fed987d6f3f9e34829861a8f4ede0fe564a2714ef0bc96968b"}
- experimental_model
- Macrophage depletion, localization and human variant assays
- exposure
- Hrg1 depletion and missense variants
- limitations
- Recycling pathway experiment; no estimate of dietary iron requirements is derived.
- nutrient_topic
- Iron research collection; topical membership is not evidence of a direct dietary effect. · Iron
- organism
- Mouse macrophages and human HRG1 variants
- plain_language
- Macrophages must move heme out of the compartment where old red cells are broken down.
- primary_references
- [iron-p23395172] HRG1 is essential for heme transport from the phagolysosome of macrophages during erythrophagocytosis. (2013). https://pubmed.ncbi.nlm.nih.gov/23395172/ DOI: 10.1016/j.cmet.2013.01.005
- tissue_or_cell_type
- Phagolysosomes during erythrophagocytosis
Iron: absorption, trafficking, iron-dependent enzymes and nutrient interactions (2026-09-17) · lines 550–561
AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Macrophage depletion, localization and human variant assays · source_derived_draft · unverified_draft
### iron-hrg1-recycling Hrg1 localized to phagolysosomal membranes during erythrophagocytosis and transported heme toward the macrophage cytoplasm. Condition category: normal nutrient_topic: Iron research collection; topical membership is not evidence of a direct dietary effect. plain_language: Macrophages must move heme out of the compartment where old red cells are broken down. organism: Mouse macrophages and human HRG1 variants tissue_or_cell_type: Phagolysosomes during erythrophagocytosis experimental_model: Macrophage depletion, localization and human variant assays limitations: Recycling pathway experiment; no estimate of dietary iron requirements is derived. exposure: Hrg1 depletion and missense variants evidence_span: {"source_cache": "artifacts/iron-research/23395172.abstract.txt", "locator": "Exact primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "9ffc7159cfb418fed987d6f3f9e34829861a8f4ede0fe564a2714ef0bc96968b", "start_char": 0, "end_char": 1074, "text_sha256": "9ffc7159cfb418fed987d6f3f9e34829861a8f4ede0fe564a2714ef0bc96968b"} [iron-p23395172] HRG1 is essential for heme transport from the phagolysosome of macrophages during erythrophagocytosis. (2013). https://pubmed.ncbi.nlm.nih.gov/23395172/ DOI: 10.1016/j.cmet.2013.01.005
Complete structured claim and evidence
The events it takes part in
A mechanism often involves more than two components. These are the full events, with every participant and its role.
Situations it appears in
Low-supply and faulty-machinery situations recorded in the chapters where this component plays a part.
In the sources
Preserved passages that mention this component, quoted exactly. Open one to read it in context.
Open hypotheses
Proposed ideas that involve this component. They are labeled as hypotheses and do not change any recorded statement.
This is a research prototype built from draft material. It is not medical advice, and its statements still await verification against the original studies.