ATP6V0A1 c.*583T>C

Variant ID: 17-40673721-T-C

NM_001130021.1(ATP6V0A1):c.*583T>C

This variant was identified in 7 publications

View GRCh38 version.




Publications:


Non-Coding RNA in the Pathogenesis, Progression and Treatment of Hypertension.

International Journal Of Molecular Sciences
Leimena, Christiana C; Qiu, Hongyu H
Publication Date: 2018-03-21

Variant appearance in text: rs938671
PubMed Link: 29561765
Variant Present in the following documents:
  • Main text
  • ijms-19-00927.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: rs938671
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



Proteogenomic analysis reveals exosomes are more oncogenic than ectosomes.

Oncotarget
Keerthikumar, Shivakumar S; Gangoda, Lahiru L; Liem, Michael M; Fonseka, Pamali P; Atukorala, Ishara I; Ozcitti, Cemil C; Mechler, Adam A; Adda, Christopher G CG; Ang, Ching-Seng CS; Mathivanan, Suresh S
Publication Date: 2015-06-20

Variant appearance in text: rs938671
PubMed Link: 25944692
Variant Present in the following documents:
  • oncotarget-06-15375-s005.xlsx, sheet 2
View BVdb publication page



The myriad essential roles of microRNAs in cardiovascular homeostasis and disease.

Genes & Diseases
Neppl, Ronald L RL; Wang, Da-Zhi DZ
Publication Date: 2014-03-01

Variant appearance in text: rs938671
PubMed Link: 25328909
Variant Present in the following documents:
  • Main text
  • main.pdf
View BVdb publication page



The regulated secretory pathway and human disease: insights from gene variants and single nucleotide polymorphisms.

Frontiers In Endocrinology
Lin, Wei-Jye WJ; Salton, Stephen R SR
Publication Date: 2013

Variant appearance in text: rs938671
PubMed Link: 23964269
Variant Present in the following documents:
  • Main text
  • fendo-04-00096.pdf
View BVdb publication page



A common genetic variant in the 3'-UTR of vacuolar H+-ATPase ATP6V0A1 creates a micro-RNA motif to alter chromogranin A processing and hypertension risk.

Circulation. Cardiovascular Genetics
Wei, Zhiyun Z; Biswas, Nilima N; Wang, Lei L; Courel, Maite M; Zhang, Kuixing K; Soler-Jover, Alex A; Taupenot, Laurent L; O'Connor, Daniel T DT
Publication Date: 2011-08-01

Variant appearance in text: rs938671
PubMed Link: 21558123
Variant Present in the following documents:
  • Main text
View BVdb publication page



Heritability and genome-wide linkage in US and australian twins identify novel genomic regions controlling chromogranin a: implications for secretion and blood pressure.

Circulation
O'Connor, Daniel T DT; Zhu, Gu G; Rao, Fangwen F; Taupenot, Laurent L; Fung, Maple M MM; Das, Madhusudan M; Mahata, Sushil K SK; Mahata, Manjula M; Wang, Lei L; Zhang, Kuixing K; Greenwood, Tiffany A TA; Shih, Pei-an Betty PA; Cockburn, Myles G MG; Ziegler, Michael G MG; Stridsberg, Mats M; Martin, Nicholas G NG; Whitfield, John B JB
Publication Date: 2008-07-15

Variant appearance in text: rs938671
PubMed Link: 18591442
Variant Present in the following documents:
  • Main text
View BVdb publication page