MFN2 c.-4-3133G>A

Variant ID: 1-12046089-G-A

NM_014874.3(MFN2):c.-4-3133G>A

This variant was identified in 6 publications

View GRCh38 version.




Publications:


Establishment and characterization of a new mantle cell lymphoma cell line with a NOTCH2 mutation, Arbo.

Ejhaem
Safa, Firas F; Rasmussen, Terri T; Lobelle-Rich, Patricia P; Collier, Stephanie S; Milligan, Nicholas N; Schmeig, John J; Schmid, Janet J; Wiewiorowski, Carol C; Totaro, Denise D; Brown, Theresa C TC; Satyavarapu, Ishwarya I; Badoo, Melody M; Ungerleider, Nathan N; Flemington, Erik K EK; Safah, Hana H; Saba, Nakhle S NS
Publication Date: 2022-11

Variant appearance in text: rs873458
PubMed Link: 36467812
Variant Present in the following documents:
  • JHA2-3-1326-s001.xlsx, sheet 1
View BVdb publication page



CASCADE: high-throughput characterization of regulatory complex binding altered by non-coding variants.

Cell Genomics
Bray, David D; Hook, Heather H; Zhao, Rose R; Keenan, Jessica L JL; Penvose, Ashley A; Osayame, Yemi Y; Mohaghegh, Nima N; Chen, Xiaoting X; Parameswaran, Sreeja S; Kottyan, Leah C LC; Weirauch, Matthew T MT; Siggers, Trevor T
Publication Date: 2022-02-09

Variant appearance in text: rs873458
PubMed Link: 35252945
Variant Present in the following documents:
  • Main text
  • nihms-1779282.pdf
View BVdb publication page



Hyperplasia suppressor gene polymorphisms and essential hypertension: a case-control association study in a central Han Chinese population.

International Journal Of Clinical And Experimental Pathology
Yan, Shan S; Lian, Xiao-Qing XQ; Wang, Si-Bo SB; Wang, Hao H; Wang, Lian-Sheng LS
Publication Date: 2020

Variant appearance in text: rs873458
PubMed Link: 32782719
Variant Present in the following documents:
  • Main text
View BVdb publication page



Association between MFN2 gene polymorphisms and the risk and prognosis of acute liver failure: a case-control study in a Chinese population.

Brazilian Journal Of Medical And Biological Research = Revista Brasileira De Pesquisas Medicas E Biologicas
Wei, Y-L YL; Tian, Q Q; Zhao, X-X XX; Qiu, G-Z GZ; Xu, Y Y
Publication Date: 2017-05-15

Variant appearance in text: rs873458
PubMed Link: 28513770
Variant Present in the following documents:
  • Main text
  • 1414-431X-bjmbr-1414-431X20175758.pdf
View BVdb publication page



Association of polymorphisms in mitofusin-2 gene with type 2 diabetes in Han Chinese.

Journal Of Biomedicine & Biotechnology
Li, Pengtao P; Zhu, Shuying S; Wu, Xiaopan X; Zhu, Xilin X; Li, Jingyun J; Pan, Liping L; Xin, Zhenhui Z; Niu, Fenghe F; Wu, Jia J; Liu, Ying Y
Publication Date: 2012

Variant appearance in text: rs873458
PubMed Link: 22778543
Variant Present in the following documents:
  • Main text
  • JBB2012-205752.pdf
View BVdb publication page



Evaluation of nine candidate genes in patients with normal tension glaucoma: a case control study.

Bmc Medical Genetics
Wolf, Christiane C; Gramer, Eugen E; Müller-Myhsok, Bertram B; Pasutto, Francesca F; Reinthal, Eva E; Wissinger, Bernd B; Weisschuh, Nicole N
Publication Date: 2009-09-15

Variant appearance in text: rs873458
PubMed Link: 19754948
Variant Present in the following documents:
  • Main text
  • 1471-2350-10-91.pdf
View BVdb publication page