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Large-scale whole-exome sequencing association studies identify rare functional variants influencing serum urate levels

Authors :
Adrienne Tin
Yong Li
Jennifer A. Brody
Teresa Nutile
Audrey Y. Chu
Jennifer E. Huffman
Qiong Yang
Ming-Huei Chen
Cassianne Robinson-Cohen
Aurélien Macé
Jun Liu
Ayşe Demirkan
Rossella Sorice
Sanaz Sedaghat
Melody Swen
Bing Yu
Sahar Ghasemi
Alexanda Teumer
Peter Vollenweider
Marina Ciullo
Meng Li
André G. Uitterlinden
Robert Kraaij
Najaf Amin
Jeroen van Rooij
Zoltán Kutalik
Abbas Dehghan
Barbara McKnight
Cornelia M. van Duijn
Alanna Morrison
Bruce M. Psaty
Eric Boerwinkle
Caroline S. Fox
Owen M. Woodward
Anna Köttgen
Source :
Nature Communications, Vol 9, Iss 1, Pp 1-11 (2018)
Publication Year :
2018
Publisher :
Nature Portfolio, 2018.

Abstract

Elevated serum urate levels are a risk factor for gout. Here, Tin et al. perform whole-exome sequencing in 19,517 individuals and detect low-frequency genetic variants in urate transporter genes, SLC22A12 and SLC2A9, associated with serum urate levels and confirm their damaging nature in vitro and in silico.

Subjects

Subjects :
Science

Details

Language :
English
ISSN :
20411723
Volume :
9
Issue :
1
Database :
Directory of Open Access Journals
Journal :
Nature Communications
Publication Type :
Academic Journal
Accession number :
edsdoj.180796564ad94848948b76417618b4ad
Document Type :
article
Full Text :
https://doi.org/10.1038/s41467-018-06620-4