HSPB7 c.333+315A>G

Variant ID: 1-16343254-T-C

NM_014424.4(HSPB7):c.333+315A>G

This variant was identified in 28 publications

View GRCh38 version.




Publications:


Role of non-coding variants in cardiovascular disease.

Journal Of Cellular And Molecular Medicine
Heshmatzad, Katayoun K; Naderi, Niloofar N; Maleki, Majid M; Abbasi, Shiva S; Ghasemi, Serwa S; Ashrafi, Nooshin N; Fazelifar, Amir Farjam AF; Mahdavi, Mohammad M; Kalayinia, Samira S
Publication Date: 2023-05-15

Variant appearance in text: rs1739843
PubMed Link: 37183561
Variant Present in the following documents:
  • Main text
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Next-generation whole exome sequencing to delineate the genetic basis of primary congenital glaucoma.

Scientific Reports
Rauf, Bushra B; Khan, Shahid Y SY; Jiao, Xiaodong X; Irum, Bushra B; Ashfaq, Ramla R; Zehra, Mubashra M; Khan, Asma A AA; Naeem, Muhammad Asif MA; Shahzad, Mohsin M; Riazuddin, Sheikh S; Hejtmancik, J Fielding JF; Riazuddin, S Amer SA
Publication Date: 2022-10-14

Variant appearance in text: rs1739843
PubMed Link: 36241656
Variant Present in the following documents:
  • 41598_2022_20939_MOESM14_ESM.xlsx, sheet 2
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Exploration of Potential Genetic Biomarkers for Heart Failure: A Systematic Review.

International Journal Of Environmental Research And Public Health
Chair, Sek Ying SY; Chan, Judy Yuet Wa JYW; Waye, Mary Miu Yee MMY; Liu, Ting T; Law, Bernard Man Hin BMH; Chien, Wai Tong WT
Publication Date: 2021-05-31

Variant appearance in text: rs1739843
PubMed Link: 34072866
Variant Present in the following documents:
  • Main text
  • ijerph-18-05904.pdf
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Advances in the Genetics and Genomics of Heart Failure.

Current Cardiology Reports
Reza, Nosheen N; Owens, Anjali Tiku AT
Publication Date: 2020-09-10

Variant appearance in text: rs1739843
PubMed Link: 32910329
Variant Present in the following documents:
  • Main text
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A genetic association study of heart failure: more evidence for the role of BAG3 in idiopathic dilated cardiomyopathy.

Esc Heart Failure
de Denus, Simon S; Mottet, Fannie F; Korol, Sandra S; Feroz Zada, Yassamin Y; Provost, Sylvie S; Mongrain, Ian I; Asselin, Géraldine G; Oussaïd, Essaïd E; Busseuil, David D; Lettre, Guillaume G; Rioux, John J; Racine, Normand N; O'Meara, Eileen E; White, Michel M; Rouleau, Jean J; Tardif, Jean Claude JC; Dubé, Marie-Pierre MP
Publication Date: 2020-12

Variant appearance in text: rs1739843
PubMed Link: 32869539
Variant Present in the following documents:
  • Main text
  • EHF2-7-4384.pdf
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A genetic association study of heart failure: more evidence for the role of BAG3 in idiopathic dilated cardiomyopathy.

Esc Heart Failure
de Denus, Simon S; Mottet, Fannie F; Korol, Sandra S; Feroz Zada, Yassamin Y; Provost, Sylvie S; Mongrain, Ian I; Asselin, Géraldine G; Oussaïd, Essaïd E; Busseuil, David D; Lettre, Guillaume G; Rioux, John J; Racine, Normand N; O'Meara, Eileen E; White, Michel M; Rouleau, Jean J; Tardif, Jean Claude JC; Dubé, Marie-Pierre MP
Publication Date: 2020-09-01

Variant appearance in text: rs1739843
PubMed Link: 32869539
Variant Present in the following documents:
  • Main text
  • EHF2-7-4384.pdf
View BVdb publication page



Sodium sensitivity of blood pressure in Chinese populations.

Journal Of Human Hypertension
Liu, Yang Y; Shi, Mengyao M; Dolan, Jacquelyn J; He, Jiang J
Publication Date: 2020-02

Variant appearance in text: rs1739843
PubMed Link: 30631129
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genetic Evidence Supporting the Role of the Calcium Channel, CACNA1S, in Tooth Cusp and Root Patterning.

Frontiers In Physiology
Laugel-Haushalter, Virginie V; Morkmued, Supawich S; Stoetzel, Corinne C; Geoffroy, Véronique V; Muller, Jean J; Boland, Anne A; Deleuze, Jean-François JF; Chennen, Kirsley K; Pitiphat, Waranuch W; Dollfus, Hélène H; Niederreither, Karen K; Bloch-Zupan, Agnès A; Pungchanchaikul, Patimaporn P
Publication Date: 2018

Variant appearance in text: HSPB7: 333+315A>G; rs1739843
PubMed Link: 30319441
Variant Present in the following documents:
  • Table_5.xlsx, sheet 1
  • Table_6.xlsx, sheet 1
View BVdb publication page



A Genome-Wide Association Study of Idiopathic Dilated Cardiomyopathy in African Americans.

Journal Of Personalized Medicine
Xu, Huichun H; Dorn, Gerald W GW; Shetty, Amol A; Parihar, Ankita A; Dave, Tushar T; Robinson, Shawn W SW; Gottlieb, Stephen S SS; Donahue, Mark P MP; Tomaselli, Gordon F GF; Kraus, William E WE; Mitchell, Braxton D BD; Liggett, Stephen B SB
Publication Date: 2018-02-26

Variant appearance in text: rs1739843
PubMed Link: 29495422
Variant Present in the following documents:
  • Main text
  • jpm-08-00011.pdf
  • jpm-08-00011-s001.pdf
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HSPB7 prevents cardiac conduction system defect through maintaining intercalated disc integrity.

Plos Genetics
Liao, Wern-Chir WC; Juo, Liang-Yi LY; Shih, Yen-Ling YL; Chen, Yen-Hui YH; Yan, Yu-Ting YT
Publication Date: 2017-08

Variant appearance in text: rs1739843
PubMed Link: 28827800
Variant Present in the following documents:
  • Main text
  • pgen.1006984.pdf
View BVdb publication page



Genomics and pharmacogenomics of salt-sensitive hypertension Minireview.

Current Hypertension Reviews
Armando, Ines I; Villar, Van Anthony M VA; Jose, Pedro A PA
Publication Date: 2015

Variant appearance in text: rs1739843
PubMed Link: 28392754
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genetics and genomics of dilated cardiomyopathy and systolic heart failure.

Genome Medicine
Tayal, Upasana U; Prasad, Sanjay S; Cook, Stuart A SA
Publication Date: 2017-02-22

Variant appearance in text: rs1739843
PubMed Link: 28228157
Variant Present in the following documents:
  • Main text
  • 13073_2017_Article_410.pdf
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Variants of resistin gene and the risk of idiopathic dilated cardiomyopathy in Pakistan.

Meta Gene
Hussain, Sabir S; Haroon, Javeria J; Ejaz, Shagufta S; Javed, Qamar Q
Publication Date: 2016-09

Variant appearance in text: rs1739843
PubMed Link: 27114921
Variant Present in the following documents:
  • Main text
  • main.pdf
View BVdb publication page



Genetic polymorphisms associated with heart failure: A literature review.

The Journal Of International Medical Research
Guo, Mengqi M; Guo, Guanlun G; Ji, Xiaoping X
Publication Date: 2016-02

Variant appearance in text: rs1739843
PubMed Link: 26769713
Variant Present in the following documents:
  • Main text
  • 10.1177_0300060515604755.pdf
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Common Variants for Heart Failure.

Current Genomics
Shen, Shutong S; Tao, Lichan L; Wang, Xiuzhi X; Kong, Xiangqing X; Li, Xinli X
Publication Date: 2015-04

Variant appearance in text: rs1739843
PubMed Link: 26085806
Variant Present in the following documents:
  • Main text
  • CG-16-82.pdf
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Genome-wide association studies of late-onset cardiovascular disease.

Journal Of Molecular And Cellular Cardiology
Smith, J Gustav JG; Newton-Cheh, Christopher C
Publication Date: 2015-06

Variant appearance in text: rs1739843
PubMed Link: 25870159
Variant Present in the following documents:
  • Main text
View BVdb publication page



Common variant rs7597774 in ADD2 is associated with dilated cardiomyopathy in Chinese Han population.

International Journal Of Clinical And Experimental Medicine
Chen, Fei F FF; Xia, Yun L YL; Xu, Cheng Q CQ; Li, Si S SS; Zhao, Yuan Y YY; Wang, Xiao J XJ; Chen, Shan S SS; Gao, Lian J LJ; Zhong, Yang Y; Tu, Xin X; Wang, Qing Q; Yang, Yan Z YZ
Publication Date: 2015

Variant appearance in text: rs1739843
PubMed Link: 25785112
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genetics of common forms of heart failure: challenges and potential solutions.

Current Opinion In Cardiology
Rau, Christoph D CD; Lusis, Aldons J AJ; Wang, Yibin Y
Publication Date: 2015-05

Variant appearance in text: rs1739843
PubMed Link: 25768955
Variant Present in the following documents:
  • Main text
View BVdb publication page



Polymorphism of ZBTB17 gene is associated with idiopathic dilated cardiomyopathy: a case control study in a Han Chinese population.

European Journal Of Medical Research
Li, Xiaoping X; Luo, Rong R; Mo, Xiaoyang X; Jiang, Rongjian R; Kong, Hong H; Hua, Wei W; Wu, Xiushan X
Publication Date: 2013-04-09

Variant appearance in text: rs1739843
PubMed Link: 23570452
Variant Present in the following documents:
  • Main text
  • 2047-783X-18-10.pdf
View BVdb publication page



Clinical considerations of heritable factors in common heart failure.

Circulation. Cardiovascular Genetics
Cappola, Thomas P TP; Dorn, Gerald W GW
Publication Date: 2011-12

Variant appearance in text: rs1739843
PubMed Link: 22187448
Variant Present in the following documents:
  • Main text
View BVdb publication page



The genomic architecture of sporadic heart failure.

Circulation Research
Dorn, Gerald W GW
Publication Date: 2011-05-13

Variant appearance in text: rs1739843
PubMed Link: 21566223
Variant Present in the following documents:
  • Main text
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A genome-wide association study identifies two loci associated with heart failure due to dilated cardiomyopathy.

European Heart Journal
Villard, Eric E; Perret, Claire C; Gary, Françoise F; Proust, Carole C; Dilanian, Gilles G; Hengstenberg, Christian C; Ruppert, Volker V; Arbustini, Eloisa E; Wichter, Thomas T; Germain, Marine M; Dubourg, Olivier O; Tavazzi, Luigi L; Aumont, Marie-Claude MC; DeGroote, Pascal P; Fauchier, Laurent L; Trochu, Jean-Noël JN; Gibelin, Pierre P; Aupetit, Jean-François JF; Stark, Klaus K; Erdmann, Jeanette J; Hetzer, Roland R; Roberts, Angharad M AM; Barton, Paul J R PJ; Regitz-Zagrosek, Vera V; , ; Aslam, Uzma U; Duboscq-Bidot, Laëtitia L; Meyborg, Matthias M; Maisch, Bernhard B; Madeira, Hugo H; Waldenström, Anders A; Galve, Enrique E; Cleland, John G JG; Dorent, Richard R; Roizes, Gerard G; Zeller, Tanja T; Blankenberg, Stefan S; Goodall, Alison H AH; Cook, Stuart S; Tregouet, David A DA; Tiret, Laurence L; Isnard, Richard R; Komajda, Michel M; Charron, Philippe P; Cambien, François F
Publication Date: 2011-05

Variant appearance in text: rs1739843
PubMed Link: 21459883
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genetics of sudden cardiac death syndromes.

Current Opinion In Cardiology
Chopra, Nagesh N; Knollmann, Björn C BC
Publication Date: 2011-05

Variant appearance in text: rs1739843
PubMed Link: 21430528
Variant Present in the following documents:
  • Main text
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Loss-of-function DNA sequence variant in the CLCNKA chloride channel implicates the cardio-renal axis in interindividual heart failure risk variation.

Proceedings Of The National Academy Of Sciences Of The United States Of America
Cappola, Thomas P TP; Matkovich, Scot J SJ; Wang, Wei W; van Booven, Derek D; Li, Mingyao M; Wang, Xuexia X; Qu, Liming L; Sweitzer, Nancy K NK; Fang, James C JC; Reilly, Muredach P MP; Hakonarson, Hakon H; Nerbonne, Jeanne M JM; Dorn, Gerald W GW
Publication Date: 2011-02-08

Variant appearance in text: rs1739843
PubMed Link: 21248228
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genetics of salt-sensitive hypertension.

Current Hypertension Reports
Sanada, Hironobu H; Jones, John E JE; Jose, Pedro A PA
Publication Date: 2011-02

Variant appearance in text: rs1739843
PubMed Link: 21058046
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genetic association study identifies HSPB7 as a risk gene for idiopathic dilated cardiomyopathy.

Plos Genetics
Stark, Klaus K; Esslinger, Ulrike B UB; Reinhard, Wibke W; Petrov, George G; Winkler, Thomas T; Komajda, Michel M; Isnard, Richard R; Charron, Philippe P; Villard, Eric E; Cambien, François F; Tiret, Laurence L; Aumont, Marie-Claude MC; Dubourg, Olivier O; Trochu, Jean-Noël JN; Fauchier, Laurent L; Degroote, Pascal P; Richter, Anette A; Maisch, Bernhard B; Wichter, Thomas T; Zollbrecht, Christa C; Grassl, Martina M; Schunkert, Heribert H; Linsel-Nitschke, Patrick P; Erdmann, Jeanette J; Baumert, Jens J; Illig, Thomas T; Klopp, Norman N; Wichmann, H-Erich HE; Meisinger, Christa C; Koenig, Wolfgang W; Lichtner, Peter P; Meitinger, Thomas T; Schillert, Arne A; König, Inke R IR; Hetzer, Roland R; Heid, Iris M IM; Regitz-Zagrosek, Vera V; Hengstenberg, Christian C
Publication Date: 2010-10-21

Variant appearance in text: rs1739843
PubMed Link: 20975947
Variant Present in the following documents:
  • Main text
  • pgen.1001167.pdf
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Association of an intronic, but not any exonic, FRMD4B sequence variant and heart failure.

Clinical And Translational Science
Matkovich, Scot J SJ; Van Booven, Derek J DJ; Cappola, Thomas P TP; Dorn, Gerald W GW
Publication Date: 2010-08

Variant appearance in text: rs1739843
PubMed Link: 20718813
Variant Present in the following documents:
  • Main text
View BVdb publication page



Common variants in HSPB7 and FRMD4B associated with advanced heart failure.

Circulation. Cardiovascular Genetics
Cappola, Thomas P TP; Li, Mingyao M; He, Jing J; Ky, Bonnie B; Gilmore, Joan J; Qu, Liming L; Keating, Brendan B; Reilly, Muredach M; Kim, Cecelia E CE; Glessner, Joseph J; Frackelton, Edward E; Hakonarson, Hakon H; Syed, Faisel F; Hindes, Anna A; Matkovich, Scot J SJ; Cresci, Sharon S; Dorn, Gerald W GW
Publication Date: 2010-04

Variant appearance in text: rs1739843
PubMed Link: 20124441
Variant Present in the following documents:
  • Main text
View BVdb publication page



Cardiac signaling genes exhibit unexpected sequence diversity in sporadic cardiomyopathy, revealing HSPB7 polymorphisms associated with disease.

The Journal Of Clinical Investigation
Matkovich, Scot J SJ; Van Booven, Derek J DJ; Hindes, Anna A; Kang, Min Young MY; Druley, Todd E TE; Vallania, Francesco L M FL; Mitra, Robi D RD; Reilly, Muredach P MP; Cappola, Thomas P TP; Dorn, Gerald W GW
Publication Date: 2010-01

Variant appearance in text: rs1739843
PubMed Link: 20038796
Variant Present in the following documents:
  • Main text
View BVdb publication page