Variant ID: 11-116620256-C-A

NM_032725.3(BUD13):c.1767-965G>T

This variant was identified in 11 publications




Publications:


Identification of female-specific genetic variants for metabolic syndrome and its component traits to improve the prediction of metabolic syndrome in females.

Bmc Medical Genetics
S Kong, YS Cho
Publication Date: 2019-06-06

Variant appearance in text: rs11216129
PubMed Link: 31170924
Variant Present in the following documents:
  • Main text
View BVdb publication page



Discovery and replication of SNP-SNP interactions for quantitative lipid traits in over 60,000 individuals.

Biodata Mining
ER Holzinger, SS Verma, CB Moore, M Hall, R De, D Gilbert-Diamond, MB Lanktree, N Pankratz, A Amuzu, A Burt, C Dale, S Dudek, CE Furlong, TR Gaunt, DS Kim, H Riess, S Sivapalaratnam, V Tragante, EPA van Iperen, A Brautbar, DS Carrell, DR Crosslin, GP Jarvik, H Kuivaniemi, IJ Kullo, EB Larson, LJ Rasmussen-Torvik, G Tromp, J Baumert, KJ Cruickshanks, M Farrall, AD Hingorani, GK Hovingh, ME Kleber, BE Klein, R Klein, W Koenig, LA Lange, W MÓ“rz, KE North, N Charlotte Onland-Moret, AP Reiner, PJ Talmud, YT van der Schouw, JG Wilson, M Kivimaki, M Kumari, JH Moore, F Drenos, FW Asselbergs, BJ Keating, MD Ritchie
Publication Date: 2017

Variant appearance in text: rs11216129
PubMed Link: 28770004
Variant Present in the following documents:
  • Main text
View BVdb publication page



Association of BUD13 polymorphisms with metabolic syndrome in Chinese population: a case-control study.

Lipids In Health And Disease
L Zhang, Y You, Y Wu, Y Zhang, M Wang, Y Song, X Liu, C Kou
Publication Date: 2017-06-28

Variant appearance in text: rs11216129
PubMed Link: 28659142
Variant Present in the following documents:
  • Main text
View BVdb publication page



Quantitative trait loci at the 11q23.3 chromosomal region related to dyslipidemia in the population of Andhra Pradesh, India.

Lipids In Health And Disease
R Pranavchand, BM Reddy
Publication Date: 2017-06-13

Variant appearance in text: rs11216129
PubMed Link: 28610615
Variant Present in the following documents:
  • 12944_2017_507_MOESM3_ESM.docx
  • 12944_2017_507_MOESM4_ESM.docx
  • aaaaaMain text
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: rs11216129
PubMed Link: 28257648
Variant Present in the following documents:
  • Main text
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: rs11216129
PubMed Link: 27827461
Variant Present in the following documents:
  • Main text
  • 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: rs11216129
PubMed Link: 27257688
Variant Present in the following documents:
  • Main text
  • pone.0153720.s002.docx
  • pone.0153720.s003.xlsx
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: rs11216129
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: rs11216129
PubMed Link: 24989072
Variant Present in the following documents:
  • Main text
View BVdb publication page



Gene-centric meta-analysis of lipid traits in African, East Asian and Hispanic populations.

Plos One
CC Elbers, Y Guo, V Tragante, EP van Iperen, MB Lanktree, BA Castillo, F Chen, LR Yanek, MK Wojczynski, YR Li, B Ferwerda, CM Ballantyne, SG Buxbaum, YD Chen, WM Chen, LA Cupples, M Cushman, Y Duan, D Duggan, MK Evans, JK Fernandes, M Fornage, M Garcia, WT Garvey, N Glazer, F Gomez, TB Harris, I Halder, VJ Howard, MF Keller, MI Kamboh, C Kooperberg, SB Kritchevsky, A LaCroix, K Liu, Y Liu, K Musunuru, AB Newman, NC Onland-Moret, J Ordovas, I Peter, W Post, S Redline, SE Reis, R Saxena, PJ Schreiner, KA Volcik, X Wang, S Yusuf, AB Zonderland, SS Anand, DM Becker, B Psaty, DJ Rader, AP Reiner, SS Rich, JI Rotter, MM Sale, MY Tsai, IB Borecki, RA Hegele, S Kathiresan, MA Nalls, HA Taylor, H Hakonarson, S Sivapalaratnam, FW Asselbergs, F Drenos, JG Wilson, BJ Keating
Publication Date: 2012

Variant appearance in text: rs11216129
PubMed Link: 23236364
Variant Present in the following documents:
  • pone.0050198.s002.pdf
View BVdb publication page



Differential allelic expression in the human genome: a robust approach to identify genetic and epigenetic cis-acting mechanisms regulating gene expression.

Plos Genetics
D Serre, S Gurd, B Ge, R Sladek, D Sinnett, E Harmsen, M Bibikova, E Chudin, DL Barker, T Dickinson, JB Fan, TJ Hudson
Publication Date: 2008-02-29

Variant appearance in text: rs11216129
PubMed Link: 18454203
Variant Present in the following documents:
  • pgen.1000006.s015.pdf
View BVdb publication page



Alternative transcript annotations:

Transcript cDNA Protein Consequence Exon Intron
ENST00000260210.4 c.1767-965G>T - intron_variant - 9/9
ENST00000375445.3 c.1365-965G>T - intron_variant - 9/9
ENST00000419189.1 c.*187-965G>T - intron_variant,NMD_transcript_variant - 3/3
NM_001159736.1 c.1365-965G>T - intron_variant - 9/9
NM_032725.4 c.1767-965G>T - intron_variant - 9/9