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Li, V. CYP11B1 Gene. Encyclopedia. Available online: https://encyclopedia.pub/entry/4379 (accessed on 29 September 2026).
Li V. CYP11B1 Gene. Encyclopedia. Available at: https://encyclopedia.pub/entry/4379. Accessed September 29, 2026.
Li, Vivi. "CYP11B1 Gene" Encyclopedia, https://encyclopedia.pub/entry/4379 (accessed September 29, 2026).
Li, V. (2020, December 23). CYP11B1 Gene. In Encyclopedia. https://encyclopedia.pub/entry/4379
Li, Vivi. "CYP11B1 Gene." Encyclopedia. Web. 23 December, 2020.
CYP11B1 Gene
Edit
This entry is adapted from the peer-reviewed paper https://medlineplus.gov/genetics/gene/cyp11b1

Cytochrome P450 Family 11 Subfamily B Member 1: The CYP11B1 gene provides instructions for making an enzyme called 11-beta-hydroxylase. 

genes

References

  1. Martinez-Aguayo A, Fardella C. Genetics of hypertensive syndrome. Horm Res.2009;71(5):253-9. doi: 10.1159/000208798.
  2. Moraitis AG, Rainey WE, Auchus RJ. Gene mutations that promote adrenalaldosterone production, sodium retention, and hypertension. Appl Clin Genet. 2013Dec 24;7:1-13. doi: 10.2147/TACG.S35571. Review.
  3. Nimkarn S, New MI. Steroid 11beta- hydroxylase deficiency congenital adrenalhyperplasia. Trends Endocrinol Metab. 2008 Apr;19(3):96-9. doi:10.1016/j.tem.2008.01.002.
  4. Parajes S, Loidi L, Reisch N, Dhir V, Rose IT, Hampel R, Quinkler M, ConwayGS, Castro-Feijóo L, Araujo-Vilar D, Pombo M, Dominguez F, Williams EL, Cole TR, Kirk JM, Kaminsky E, Rumsby G, Arlt W, Krone N. Functional consequences of seven novel mutations in the CYP11B1 gene: four mutations associated with nonclassicand three mutations causing classic 11{beta}-hydroxylase deficiency. J ClinEndocrinol Metab. 2010 Feb;95(2):779-88. doi: 10.1210/jc.2009-0651.
  5. Peter M. Congenital adrenal hyperplasia: 11beta-hydroxylase deficiency. Semin Reprod Med. 2002 Aug;20(3):249-54. Review.
  6. Quack I, Vonend O, Rump LC. Familial hyperaldosteronism I-III. Horm Metab Res.2010 Jun;42(6):424-8. doi: 10.1055/s-0029-1246187.
  7. Stowasser M, Gordon RD. Familial hyperaldosteronism. J Steroid Biochem MolBiol. 2001 Sep;78(3):215-29. Review.
  8. Stowasser M, Gordon RD. Monogenic mineralocorticoid hypertension. Best PractRes Clin Endocrinol Metab. 2006 Sep;20(3):401-20. Review.
  9. Stowasser M, Gunasekera TG, Gordon RD. Familial varieties of primaryaldosteronism. Clin Exp Pharmacol Physiol. 2001 Dec;28(12):1087-90. Review.
  10. Williams SS. Advances in genetic hypertension. Curr Opin Pediatr. 2007Apr;19(2):192-8. Review.
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Subjects: Genetics & Heredity
Contributor MDPI registered users' name will be linked to their SciProfiles pages. To register with us, please refer to https://encyclopedia.pub/register : Vivi Li
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Entry Collection: MedlinePlus
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Update Date: 23 Dec 2020
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