Homo sapiens cytochrome P450 family 11 subfamily B member 1 (CYP11B1), - Nucleotide

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Molecular analysis of 12 Chinese patients with 11β-hydroxylase deficiency and in vitro functional study of 20 CYP11B1 missense variants. [FASEB J. 2023]
Molecular analysis of 12 Chinese patients with 11β-hydroxylase deficiency and in vitro functional study of 20 CYP11B1 missense variants.
Sun B, Lu L, Xie S, Zhang W, Zhang X, Tong A, Chen S, Wu X, Mao J, Wang X, et al. FASEB J. 2023 Apr; 37(4):e22869.
Genetic variants in CYP11B1 influence the susceptibility to coronary heart disease. [BMC Med Genomics. 2022]
Genetic variants in CYP11B1 influence the susceptibility to coronary heart disease.
Huang X, Cheng Y, Wang N. BMC Med Genomics. 2022 Jul 13; 15(1):158. Epub 2022 Jul 13.
GRAde: a long-read sequencing approach to efficiently identifying the CYP11B1/CYP11B2 chimeric form in patients with glucocorticoid-remediable aldosteronism. [BMC Bioinformatics. 2022]
GRAde: a long-read sequencing approach to efficiently identifying the CYP11B1/CYP11B2 chimeric form in patients with glucocorticoid-remediable aldosteronism.
Wu YC, Chen CI, Chen PY, Kuo CH, Hung YH, Peng KY, Wu VC, Tsai-Wu JJ, Hsu CL, TAIPAI group. BMC Bioinformatics. 2022 Jan 10; 22(Suppl 10):613. Epub 2022 Jan 10.

RefSeq alternative splicing
See 2 reference mRNA sequence splice variants for the CYP11B1 gene.

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Nucleotide