RecName: Full=Cytochrome P450 11B1, mitochondrial; Short=CYP11B1; AltN - Protein

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[Analysis of a family with 11β-hydroxylase deficiency due to a mutation in the CYP11B1 gene]. [Zhonghua Yi Xue Za Zhi. 2024]
[Analysis of a family with 11β-hydroxylase deficiency due to a mutation in the CYP11B1 gene].
Yu YY, Tao YK, Hou JZ, Zhou GX, Du JJ, Zhang D. Zhonghua Yi Xue Za Zhi. 2024 Jun 11; 104(22):2074-2078.
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.
Clinical and molecular characterization of 10 Chinese children with congenital adrenal hyperplasia due to 11beta-hydroxylase deficiency. [World J Pediatr. 2024]
Clinical and molecular characterization of 10 Chinese children with congenital adrenal hyperplasia due to 11beta-hydroxylase deficiency.
Lu WL, Ma XY, Zhang J, Wang JQ, Zhang TT, Ye L, Xiao Y, Dong ZY, Wang W, Sun SY, et al. World J Pediatr. 2024 Apr; 20(4):422-433. Epub 2023 Jul 24.

RefSeq genomic sequence
See the genomic reference sequence for the CYP11B1 gene (NG_007954.1).
RefSeq protein isoforms
See 2 reference sequence protein isoforms for the CYP11B1 gene.

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P15538 [Domain Mapping of Disease Mut...]
P15538
Domain Mapping of Disease Mutations
Transcript/Protein Information [PANTHER Classification System]
Transcript/Protein Information
PANTHER Classification System
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reagents [ExactAntigen/Labome]
reagents
ExactAntigen/Labome

PREDICTED: Homo sapiens sideroflexin 2 (SFXN2), transcript variant X8, mRNA
PREDICTED: Homo sapiens sideroflexin 2 (SFXN2), transcript variant X8, mRNA
gi|2217275414|ref|XM_047424573.1|

Nucleotide
Saccharomyces cerevisiae S288C chromosome XI, complete sequence
Saccharomyces cerevisiae S288C chromosome XI, complete sequence
gi|330443667|ref|NC_001143.9||gnl|A F_000146045.2|XI

Nucleotide

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Protein