Variant ID: 11-116624703-G-T

NM_032725.3(BUD13):c.1766+3159C>A

This variant was identified in 14 publications




Publications:


A comprehensive study of metabolite genetics reveals strong pleiotropy and heterogeneity across time and context.

Nature Communications
A Gallois, J Mefford, A Ko, A Vaysse, H Julienne, M Ala-Korpela, M Laakso, N Zaitlen, P Pajukanta, H Aschard
Publication Date: 2019-10-21

Variant appearance in text: rs180326
PubMed Link: 31636271
Variant Present in the following documents:
  • 41467_2019_12703_MOESM3_ESM.xlsx
View BVdb publication page



Susceptibility loci for metabolic syndrome and metabolic components identified in Han Chinese: a multi-stage genome-wide association study.

Journal Of Cellular And Molecular Medicine
Y Zhu, D Zhang, D Zhou, Z Li, Z Li, L Fang, M Yang, Z Shan, H Li, J Chen, X Zhou, W Ye, S Yu, H Li, L Cai, C Liu, J Zhang, L Wang, Y Lai, L Ruan, Z Sun, S Zhang, H Wang, Y Liu, Y Xu, J Ling, C Xu, Y Zhang, D Lv, Z Yuan, J Zhang, Y Zhang, Y Shi, M Lai
Publication Date: 2017-06

Variant appearance in text: rs180326
PubMed Link: 28371326
Variant Present in the following documents:
  • Main text
  • JCMM-21-1106-s001.docx
View BVdb publication page



Genetic determinants of clinical heterogeneity of the coronary artery disease in the population of Hyderabad, India.

Human Genomics
R Pranavchand, AS Kumar, BM Reddy
Publication Date: 2017-03-04

Variant appearance in text: rs180326
PubMed Link: 28257648
Variant Present in the following documents:
  • Main text
View BVdb publication page



Admixture mapping in two Mexican samples identifies significant associations of locus ancestry with triglyceride levels in the BUD13/ZNF259/APOA5 region and fine mapping points to rs964184 as the main driver of the association signal.

Plos One
EJ Parra, A Mazurek, CR Gignoux, A Sockell, M Agostino, AP Morris, LE Petty, CL Hanis, NJ Cox, A Valladares-Salgado, JE Below, M Cruz
Publication Date: 2017

Variant appearance in text: rs180326
PubMed Link: 28245265
Variant Present in the following documents:
  • pone.0172880.s002.xlsx
View BVdb publication page



Association and interaction of APOA5, BUD13, CETP, LIPA and health-related behavior with metabolic syndrome in a Taiwanese population.

Scientific Reports
E Lin, PH Kuo, YL Liu, AC Yang, CF Kao, SJ Tsai
Publication Date: 2016-11-09

Variant appearance in text: rs180326
PubMed Link: 27827461
Variant Present in the following documents:
  • srep36830-s1.pdf
View BVdb publication page



Distinct Patterns of Association of Variants at 11q23.3 Chromosomal Region with Coronary Artery Disease and Dyslipidemia in the Population of Andhra Pradesh, India.

Plos One
R Pranav Chand, AS Kumar, K Anuj, S Vishnupriya, B Mohan Reddy
Publication Date: 2016

Variant appearance in text: rs180326
PubMed Link: 27257688
Variant Present in the following documents:
  • Main text
  • pone.0153720.s002.docx
  • pone.0153720.s003.xlsx
View BVdb publication page



INTEGRATING CLINICAL LABORATORY MEASURES AND ICD-9 CODE DIAGNOSES IN PHENOME-WIDE ASSOCIATION STUDIES.

Pacific Symposium On Biocomputing. Pacific Symposium On Biocomputing
A Verma, JB Leader, SS Verma, A Frase, J Wallace, S Dudek, DR Lavage, CV Van Hout, FE Dewey, J Penn, A Lopez, JD Overton, DJ Carey, DH Ledbetter, HL Kirchner, MD Ritchie, SA Pendergrass
Publication Date: 2016

Variant appearance in text: rs180326
PubMed Link: 26776183
Variant Present in the following documents:
  • NIHMS742521-supplement-2.pdf
View BVdb publication page



Genetics of kidney disease and related cardiometabolic phenotypes in Zuni Indians: the Zuni Kidney Project.

Frontiers In Genetics
SL Laston, VS Voruganti, K Haack, VO Shah, A Bobelu, J Bobelu, D Ghahate, AM Harford, SS Paine, F Tentori, SA Cole, JW MacCluer, AG Comuzzie, PG Zager
Publication Date: 2015

Variant appearance in text: rs180326
PubMed Link: 25688259
Variant Present in the following documents:
  • Main text
View BVdb publication page



Association between the MLX interacting protein-like, BUD13 homolog and zinc finger protein 259 gene polymorphisms and serum lipid levels.

Scientific Reports
LH Aung, RX Yin, JZ Wu, DF Wu, W Wang, H Li
Publication Date: 2014-07-03

Variant appearance in text: rs180326
PubMed Link: 24989072
Variant Present in the following documents:
  • Main text
View BVdb publication page



A genome-wide association study identifies PLCL2 and AP3D1-DOT1L-SF3A2 as new susceptibility loci for myocardial infarction in Japanese.

European Journal Of Human Genetics : Ejhg
M Hirokawa, H Morita, T Tajima, A Takahashi, K Ashikawa, F Miya, D Shigemizu, K Ozaki, Y Sakata, D Nakatani, S Suna, Y Imai, T Tanaka, T Tsunoda, K Matsuda, T Kadowaki, Y Nakamura, R Nagai, I Komuro, M Kubo
Publication Date: 2015-03

Variant appearance in text: rs180326
PubMed Link: 24916648
Variant Present in the following documents:
  • ejhg2014110x4.pdf
View BVdb publication page



Association of the variants in the BUD13-ZNF259 genes and the risk of hyperlipidaemia.

Journal Of Cellular And Molecular Medicine
LH Aung, RX Yin, DF Wu, W Wang, CW Liu, SL Pan
Publication Date: 2014-07

Variant appearance in text: rs180326
PubMed Link: 24780069
Variant Present in the following documents:
  • Main text
View BVdb publication page



Association of genetic variants influencing lipid levels with coronary artery disease in Japanese individuals.

Plos One
F Takeuchi, M Isono, T Katsuya, M Yokota, K Yamamoto, T Nabika, K Shimokawa, E Nakashima, T Sugiyama, H Rakugi, S Yamaguchi, T Ogihara, Y Yamori, N Kato
Publication Date: 2012

Variant appearance in text: rs180326
PubMed Link: 23050023
Variant Present in the following documents:
  • pone.0046385.s003.xls
  • pone.0046385.s004.xls
  • pone.0046385.s005.xls
View BVdb publication page



A replication study of GWAS-derived lipid genes in Asian Indians: the chromosomal region 11q23.3 harbors loci contributing to triglycerides.

Plos One
TR Braun, LF Been, A Singhal, J Worsham, S Ralhan, GS Wander, JC Chambers, JS Kooner, CE Aston, DK Sanghera
Publication Date: 2012

Variant appearance in text: rs180326
PubMed Link: 22623978
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genome-wide association study identifies common variants associated with circulating vitamin E levels.

Human Molecular Genetics
JM Major, K Yu, W Wheeler, H Zhang, MC Cornelis, ME Wright, M Yeager, K Snyder, SJ Weinstein, A Mondul, H Eliassen, M Purdue, A Hazra, CA McCarty, S Hendrickson, J Virtamo, D Hunter, S Chanock, P Kraft, D Albanes
Publication Date: 2011-10-01

Variant appearance in text: rs180326
PubMed Link: 21729881
Variant Present in the following documents:
  • Main text
View BVdb publication page



Alternative transcript annotations:

Transcript cDNA Protein Consequence Exon Intron
ENST00000260210.4 c.1766+3159C>A - intron_variant - 9/9
ENST00000375445.3 c.1364+3159C>A - intron_variant - 9/9
ENST00000419189.1 c.*186+3159C>A - intron_variant,NMD_transcript_variant - 3/3
NM_001159736.1 c.1364+3159C>A - intron_variant - 9/9
NM_032725.4 c.1766+3159C>A - intron_variant - 9/9