The genomic landscape of <i>CYP2D6</i> variation in the Indian population-Reference-Cited by-同舟云学术

The genomic landscape of CYP2D6 variation in the Indian population

Published:2024-02 Issue:3 Volume:25 Page:147-160
ISSN:1462-2416
Container-title:Pharmacogenomics
language:en
Short-container-title:Pharmacogenomics

Author:

Sivadas Ambily¹^ORCID,Rathore Surabhi²³^ORCID,Sahana S²³^ORCID,Jolly Bani²³^ORCID,Bhoyar Rahul C²,Jain Abhinav²³^ORCID,Sharma Disha²^ORCID,Imran Mohamed²³,Senthilvel Vigneshwar²³,Divakar Mohit Kumar²³^ORCID,Mishra Anushree²³,Sivasubbu Sridhar²³⁴^ORCID,Scaria Vinod²³⁴^ORCID

Affiliation:

1. Division of Nutrition, St. John’s Research Institute, St. John’s National Academy of Health Sciences, Bangalore, Karnataka, 560034, India

2. CSIR Institute of Genomics & Integrative Biology, Mathura Road, New Delhi, 110025, India

3. Academy of Scientific & Innovative Research (AcSIR), Ghaziabad, Uttar Pradesh, 201002, India

4. Vishwanath Cancer Care Foundation, B 702, 7th Floor, Neelkanth Business Park Kirol Village, Vidya Vihar, West Mumbai, 400086, India

Funder

Council of Scientific and Industrial Research, India

Publisher

Informa UK Limited

Link

https://www.tandfonline.com/doi/pdf/10.2217/pgs-2023-0233

Reference52 articles.

1. The P450 Superfamily: Update on New Sequences, Gene Mapping, Accession Numbers, Early Trivial Names of Enzymes, and Nomenclature

2. The Pharmacogene Variation (PharmVar) Consortium: Incorporation of the Human Cytochrome P450 (CYP ) Allele Nomenclature Database

3. The human debrisoquine 4-hydroxylase (CYP2D) locus: sequence and identification of the polymorphic CYP2D6 gene, a related gene, and a pseudogene;Kimura S;Am. J. Hum. Genet.,1989

4. Deletion of the entire cytochrome P450 CYP2D6 gene as a cause of impaired drug metabolism in poor metabolizers of the debrisoquine/sparteine polymorphism;Gaedigk A;Am. J. Hum. Genet.,1991

5. Multiple mutations of the human cytochrome P450IID6 gene (CYP2D6) in poor metabolizers of debrisoquine. Study of the functional significance of individual mutations by expression of chimeric genes.