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    Topic review

    TFR2 Gene

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    (This entry belongs to Entry Collection "MedlinePlus ")

    Definition

    Transferrin receptor 2: The TFR2 gene provides instructions for making a protein called transferrin receptor 2. 

    1. Normal Function

    The TFR2 gene provides instructions for making a protein called transferrin receptor 2. The main function of this protein is to help iron enter liver cells (hepatocytes). On the surface of hepatocytes, the receptor binds to a protein called transferrin, which transports iron through the blood to tissues throughout the body. When transferrin binds to transferrin receptor 2, iron is allowed to enter the cell.

    Additionally, transferrin receptor 2 can bind to other proteins to help regulate iron storage levels in the body by controlling the levels of another protein called hepcidin. Hepcidin is a protein that determines how much iron is absorbed from the diet and released from storage sites in the body in response to iron levels.

    2. Health Conditions Related to Genetic Changes

    2.1. Hereditary hemochromatosis

    About 50 mutations in the TFR2 gene cause type 3 hemochromatosis, a form of hereditary hemochromatosis that begins in early adulthood, usually before age 30. Hereditary hemochromatosis is a disorder that causes the body to absorb too much iron from the diet. The excess iron accumulates in, and eventually damages, the body's tissues and organs.

    Some TFR2 gene mutations prevent the production of transferrin receptor 2. Other mutations result in proteins that have an incorrect sequence of protein building blocks (amino acids) or proteins that are too short to function normally. These mutations prevent the protein from binding to transferrin, blocking iron from entering hepatocytes.

    Mutations in the TFR2 gene are also thought to contribute to low levels of hepcidin in the body, which results in too much iron being absorbed from the diet. When this occurs, the excess iron is stored in the body's tissues, especially the liver. Iron overload leads to the organ damage and other signs and symptoms of type 3 hemochromatosis.

    3. Other Names for This Gene

    • HFE3
    • TFR2_HUMAN
    • Transferrin Receptor Protein 2

    This entry is adapted from https://medlineplus.gov/genetics/gene/tfr2

    References

    1. Camaschella C, Roetto A, Calì A, De Gobbi M, Garozzo G, Carella M, Majorano N,Totaro A, Gasparini P. The gene TFR2 is mutated in a new type of haemochromatosismapping to 7q22. Nat Genet. 2000 May;25(1):14-5.
    2. Deicher R, Hörl WH. New insights into the regulation of iron homeostasis. Eur J Clin Invest. 2006 May;36(5):301-9. Review.
    3. Gerhard GS, Paynton BV, DiStefano JK. Identification of Genes for HereditaryHemochromatosis. Methods Mol Biol. 2018;1706:353-365. doi:10.1007/978-1-4939-7471-9_19. Review.
    4. Kleven MD, Jue S, Enns CA. Transferrin Receptors TfR1 and TfR2 BindTransferrin through Differing Mechanisms. Biochemistry. 2018 Mar6;57(9):1552-1559. doi: 10.1021/acs.biochem.8b00006.
    5. Le Gac G, Mons F, Jacolot S, Scotet V, Férec C, Frébourg T. Early onsethereditary hemochromatosis resulting from a novel TFR2 gene nonsense mutation(R105X) in two siblings of north French descent. Br J Haematol. 2004Jun;125(5):674-8.
    6. Peters TM, Meulders AF, Redert K, Cuijpers ML, Rennings AJ, Janssen MC,Blijlevens NM, Swinkels DW. TFR2-related haemochromatosis in the Netherlands: acause of arthralgia in young adulthood. Neth J Med. 2017 Mar;75(2):56-64.
    7. Pietrangelo A. Non-HFE hemochromatosis. Semin Liver Dis. 2005Nov;25(4):450-60. Review.
    8. Roetto A, Daraio F, Alberti F, Porporato P, Calì A, De Gobbi M, Camaschella C.Hemochromatosis due to mutations in transferrin receptor 2. Blood Cells Mol Dis. 2002 Nov-Dec;29(3):465-70.
    9. Trinder D, Baker E. Transferrin receptor 2: a new molecule in iron metabolism.Int J Biochem Cell Biol. 2003 Mar;35(3):292-6. Review.
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