IL12RB1 Gene

Last updated on: 01.04.2022

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DefinitionThis section has been translated automatically.

IL12RB1 (IL12RB1 stands for "Interleukin 12 Receptor Subunit Beta 1") is a protein coding gene located on chromosome 19p13.11. The protein encoded by the IL12RB1 gene is a type I transmembrane protein that belongs to the hemopoietin receptor superfamily. This protein binds with low affinity to interleukin 12 (IL12) and is thought to be part of the IL12 receptor complex. The protein forms a disulfide-linked oligomer that is required for its IL12-binding activity.

Coexpression of this protein and IL12RB2 has been shown to lead to the formation of functional, high-affinity receptors for IL12. These are necessary for IL12-dependent signal transduction. Mutations in this gene impair the development of interleukin-17-producing T lymphocytes and lead to increased susceptibility to mycobacterial and Salmonella infections.

Clinical pictureThis section has been translated automatically.

Diseases associated with IL12RB1 include:

  • Immunodeficiency 30.

LiteratureThis section has been translated automatically.

  1. Al-Muhsen S et al (2008) The genetic heterogeneity of mendelian susceptibility to mycobacterial diseases. J Allergy Clin Immun 122: 1043-1051.
  2. Altare F et al (1998) Impairment of mycobacterial immunity in human interleukin-12 receptor deficiency. Science 280: 1432-1435.
  3. de Jong R et al. (1998) Severe mycobacterial and Salmonella infections in interleukin-12 receptor-deficient patients. Science 280: 1435-1438.
  4. Fieschi C et al (2003) Low penetrance, broad resistance, and favorable outcome of interleukin 12 receptor beta-1 deficiency: medical and immunological implications. J Exp Med 197: 527-535.
  5. Ozbek N et al (2005) Interleukin-12 receptor beta-1 chain deficiency in a child with disseminated tuberculosis. Clin. Infect. Dis 40: e55-e58.
  6. Picard C et al. (2015) Primary immunodeficiency diseases: an update on the classification from the International Union of Immunological Societies Expert Committee for Primary Immunodeficiency 2015. J Clin Immunol 35:696-726.
  7. Yazdani R et al (2020) Common variable immunodeficiency: epidemiology, pathogenesis, clinical manifestations, diagnosis, classification, and management. J Investig Allergol Clin Immunol 30:14-34.

Last updated on: 01.04.2022