Varaico: Literature-Extracted Genetic Variants

Gene:CYP11A1
Variant:p.L141W
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CYP11A1

NM_000781.3:p.L141W

Associated Papers

A CYP11A1 homozygous exonic variant inducing an alternative splicing, frameshift and truncation in a family with congenital adrenal hyperplasia.

Alhamoudi KM et al.

Heliyon, 2024

39157388 (PubMed )
Supplement: mmc1.docx

Engineering of a high-fidelity Cas12a nuclease variant capable of allele-specific editing.

Wei J et al.

Plos Biology, 2024

38865309 (PubMed )
Supplement: pbio.3002680.s016.xlsx › ClinVar

Exploring the impact of CYP11A1's missense SNPs on the interaction between CYP11A1 and cholesterol: A comprehensive structural analysis and MD simulation study.

Redouane S et al.

Computational Biology and Chemistry, 2023

Side-chain cleavage enzyme deficiency: Systematic review and case series.

Phadte A et al.

Clinical Endocrinology, 2023

Predicted Benign and Synonymous Variants in CYP11A1 Cause Primary Adrenal Insufficiency Through Missplicing.

Maharaj A et al.

Journal of the Endocrine Society, 2019

30620006 (PubMed )
Supplement: js.2018-00130.st1.docx

MitoFates: improved prediction of mitochondrial targeting sequences and their cleavage sites.

Fukasawa Y et al.

Molecular & Cellular Proteomics : Mcp, 2015

25670805 (PubMed )
Supplement: supp_M114.043083_mcp.M114.043083-16.xlsx › TableS9A

Cytochromes p450: roles in diseases.

Pikuleva IA et al.

The Journal of Biological Chemistry, 2013

Varied clinical presentations of seven patients with mutations in CYP11A1 encoding the cholesterol side-chain cleavage enzyme, P450scc.

Tee MK et al.

The Journal of Clinical Endocrinology and Metabolism, 2013

Delayed diagnosis of adrenal insufficiency in a patient with severe penoscrotal hypospadias due to two novel P450 side-change cleavage enzyme (CYP11A1) mutations (p.R360W; p.R405X).

Parajes S et al.

European Journal of Endocrinology, 2012

A novel entity of clinically isolated adrenal insufficiency caused by a partially inactivating mutation of the gene encoding for P450 side chain cleavage enzyme (CYP11A1).

Parajes S et al.

The Journal of Clinical Endocrinology and Metabolism, 2011

Partial defect in the cholesterol side-chain cleavage enzyme P450scc (CYP11A1) resembling nonclassic congenital lipoid adrenal hyperplasia.

Sahakitrungruang T et al.

The Journal of Clinical Endocrinology and Metabolism, 2011

P450 side-chain cleavage deficiency--a rare cause of congenital adrenal hyperplasia.

Hauffa B et al.

Endocrine Development, 2011

Severe combined adrenal and gonadal deficiency caused by novel mutations in the cholesterol side chain cleavage enzyme, P450scc.

Kim CJ et al.

The Journal of Clinical Endocrinology and Metabolism, 2008

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Regarding the variants extracted from papers and shown text snippets from research papers, the following holds: "Some rights reserved. This work permits non-commercial use, distribution and reproduction in any medium, provided the original author and source are credited."