HSPA5 c.*1568C>T

Variant ID: 9-127997303-G-A

NM_005347.4(HSPA5):c.*1568C>T

This variant was identified in 14 publications

View GRCh38 version.




Publications:


Multifactor dimensionality reduction method identifies novel SNP interactions in the WNT protein interaction networks that are associated with recurrence risk in colorectal cancer.

Frontiers In Oncology
Curtis, Aaron A AA; Yu, Yajun Y; Carey, Megan M; Parfrey, Patrick P; Yilmaz, Yildiz E YE; Savas, Sevtap S
Publication Date: 2023

Variant appearance in text: rs12009
PubMed Link: 36998434
Variant Present in the following documents:
  • fonc-13-1122229.pdf
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Genetic polymorphisms of Ca2+ transport proteins and molecular chaperones in mitochondria-associated endoplasmic reticulum membrane and non-alcoholic fatty liver disease.

Frontiers In Endocrinology
Tang, Zongzhe Z; Ding, Yajie Y; Zhang, Ru R; Zhang, Mengting M; Guan, Qing Q; Zhang, Liuxin L; Wang, Hongliang H; Chen, Yue Y; Jiang, Rong R; Zhang, Wei W; Wang, Jie J
Publication Date: 2022

Variant appearance in text: rs12009
PubMed Link: 36686460
Variant Present in the following documents:
  • Main text
  • fendo-13-1056283.pdf
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Beneficial effects of mifepristone treatment in breast cancer patients selected by the progesterone receptor isoform ratio: Results from the MIPRA trial.

Clinical Cancer Research : An Official Journal Of The American Association For Cancer Research
Elía, Andrés A; Saldain, Leo L; Vanzulli, Silvia I SI; Helguero, Luisa A LA; Lamb, Caroline A CA; Fabris, Victoria V; Pataccini, Gabriela G; Martínez-Vazquez, Paula P; Burruchaga, Javier J; Caillet-Bois, Ines I; Spengler, Eunice E; Acosta Haab, Gabriela G; Liguori, Marcos M; Castets, Alejandra A; Lovisi, Silvia S; Abascal, María F MF; Novaro, Virginia V; Sánchez, Jana J; Muñoz, Javier J; Belizán, Jose M JM; Abba, Martín C MC; Gass, Hugo H; Rojas, Paola P; Lanari, Claudia C
Publication Date: 2022-10-21

Variant appearance in text: rs12009
PubMed Link: 36269797
Variant Present in the following documents:
  • ccr-22-2060_supplementary_table_s5_suppts5.xlsx, sheet 1
View BVdb publication page



MicroRNA-binding site polymorphisms and risk of colorectal cancer: A systematic review and meta-analysis.

Cancer Medicine
Gholami, Morteza M; Larijani, Bagher B; Sharifi, Farshad F; Hasani-Ranjbar, Shirin S; Taslimi, Reza R; Bastami, Milad M; Atlasi, Rasha R; Amoli, Mahsa M MM
Publication Date: 2019-12

Variant appearance in text: rs12009
PubMed Link: 31637880
Variant Present in the following documents:
  • Main text
  • CAM4-8-7477.pdf
View BVdb publication page



Proteogenomic analysis prioritises functional single nucleotide variants in cancer samples.

Oncotarget
Ma, Shiyong S; Menon, Ranjeeta R; Poulos, Rebecca C RC; Wong, Jason W H JWH
Publication Date: 2017-11-10

Variant appearance in text: rs12009
PubMed Link: 29221171
Variant Present in the following documents:
  • oncotarget-08-95841-s002.xlsx, sheet 1
  • oncotarget-08-95841-s002.xlsx, sheet 4
View BVdb publication page



Identification of EML4-ALK as an alternative fusion gene in epithelioid inflammatory myofibroblastic sarcoma.

Orphanet Journal Of Rare Diseases
Jiang, Quan Q; Tong, Han-Xing HX; Hou, Ying-Yong YY; Zhang, Yong Y; Li, Jing-Lei JL; Zhou, Yu-Hong YH; Xu, Jing J; Wang, Jiong-Yuan JY; Lu, Wei-Qi WQ
Publication Date: 2017-05-23

Variant appearance in text: rs12009
PubMed Link: 28535796
Variant Present in the following documents:
  • 13023_2017_647_MOESM1_ESM.xlsx, sheet 4
View BVdb publication page



Multivariate Genetic Correlates of the Auditory Paired Stimuli-Based P2 Event-Related Potential in the Psychosis Dimension From the BSNIP Study.

Schizophrenia Bulletin
Mokhtari, Mohammadreza M; Narayanan, Balaji B; Hamm, Jordan P JP; Soh, Pauline P; Calhoun, Vince D VD; Ruaño, Gualberto G; Kocherla, Mohan M; Windemuth, Andreas A; Clementz, Brett A BA; Tamminga, Carol A CA; Sweeney, John A JA; Keshavan, Matcheri S MS; Pearlson, Godfrey D GD
Publication Date: 2016-05

Variant appearance in text: rs12009
PubMed Link: 26462502
Variant Present in the following documents:
  • Main text
View BVdb publication page



Polymorphisms of glucose-regulated protein 78 and risk of colorectal cancer: a case-control study in southwest China.

Plos One
Zhang, Dan D; Zhou, Bin B; Li, Yuan Y; Wang, Mojin M; Wang, Cun C; Zhou, Zongguang Z; Sun, Xiaofeng X
Publication Date: 2013

Variant appearance in text: rs12009
PubMed Link: 23818965
Variant Present in the following documents:
  • Main text
  • pone.0066791.pdf
View BVdb publication page



Linkage analysis of plasma dopamine β-hydroxylase activity in families of patients with schizophrenia.

Human Genetics
Cubells, Joseph F JF; Sun, Xiangqing X; Li, Wenbiao W; Bonsall, Robert W RW; McGrath, John A JA; Avramopoulos, Dimitri D; Lasseter, Virginia K VK; Wolyniec, Paula S PS; Tang, Yi-Lang YL; Mercer, Kristina K; Pulver, Ann E AE; Elston, Robert C RC
Publication Date: 2011-11

Variant appearance in text: rs12009
PubMed Link: 21509519
Variant Present in the following documents:
  • Main text
View BVdb publication page



The 3' UTR variants in the GRP78 are not associated with overall survival in resectable hepatocellular carcinoma.

Plos One
Zhu, Xiao X; Wang, Fang F; Lin, Marie C M MC; Tian, Linwei L; Fan, Wenguo W; Ng, Samuel S SS; Liu, Minjuan M; Huang, Jianqing J; Xu, Zhenhua Z; Li, Dongpei D; Kung, Hsiangfu H
Publication Date: 2011-03-22

Variant appearance in text: rs12009
PubMed Link: 21445355
Variant Present in the following documents:
  • Main text
  • pone.0017783.pdf
View BVdb publication page



GRP78 promoter polymorphism rs391957 as potential predictor for clinical outcome in gastric and colorectal cancer patients.

Annals Of Oncology : Official Journal Of The European Society For Medical Oncology
Winder, T T; Bohanes, P P; Zhang, W W; Yang, D D; Power, D G DG; Ning, Y Y; Gerger, A A; Wilson, P M PM; Tang, L H LH; Shah, M M; Lee, A S AS; Lenz, H-J HJ
Publication Date: 2011-11

Variant appearance in text: rs12009
PubMed Link: 21382870
Variant Present in the following documents:
  • Main text
View BVdb publication page



Application of systems biology approach identifies and validates GRB2 as a risk gene for schizophrenia in the Irish Case Control Study of Schizophrenia (ICCSS) sample.

Schizophrenia Research
Sun, Jingchun J; Wan, Chunling C; Jia, Peilin P; Fanous, Ayman H AH; Kendler, Kenneth S KS; Riley, Brien P BP; Zhao, Zhongming Z
Publication Date: 2011-02

Variant appearance in text: rs12009
PubMed Link: 21195589
Variant Present in the following documents:
  • Main text
View BVdb publication page



Lack of association between the GRP78 polymorphisms in the promoter and 3' UTR and susceptibility to chronic HBV infection in a Chinese Han population.

Bmc Medical Genetics
Zhu, Xiao X; Li, Dong-Pei DP; Fan, Wen-Guo WG; Lin, Marie C M MC; Wang, Jin-Long JL; Lin, Sheng-Qu SQ; Huang, Jian-Qing JQ; Kung, Hsiang-Fu HF
Publication Date: 2010-06-02

Variant appearance in text: rs12009
PubMed Link: 20525207
Variant Present in the following documents:
  • Main text
View BVdb publication page



An international collaborative family-based whole-genome linkage scan for high-grade myopia.

Investigative Ophthalmology & Visual Science
Li, Yi-Ju YJ; Guggenheim, Jeremy A JA; Bulusu, Anuradha A; Metlapally, Ravikanth R; Abbott, Diana D; Malecaze, Francois F; Calvas, Patrick P; Rosenberg, Thomas T; Paget, Sandrine S; Creer, Rosalind C RC; Kirov, George G; Owen, Michael J MJ; Zhao, Bei B; White, Tristan T; Mackey, David A DA; Young, Terri L TL
Publication Date: 2009-07

Variant appearance in text: rs12009
PubMed Link: 19324860
Variant Present in the following documents:
  • Main text
View BVdb publication page