Homo sapiens cytochrome P450, family 11, subfamily B, polypeptide 1 (C - Nucleotide

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Identification and functional characterization of compound heterozygous CYP11B1 gene mutations. [Endocrine. 2024]
Identification and functional characterization of compound heterozygous CYP11B1 gene mutations.
Liu H, Liu F, Wei Z, Liu P, Liu Q, Chen L, Hou X. Endocrine. 2024 Apr; 84(1):253-264. Epub 2024 Jan 29.
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.

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

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Nucleotide