TEX14 c.137-1171G>A

Variant ID: 17-56709086-C-T

NM_031272.4(TEX14):c.137-1171G>A

This variant was identified in 3 publications

View GRCh38 version.




Publications:


Gene regulatory effects of disease-associated variation in the NRF2 network.

Current Opinion In Toxicology
Lacher, Sarah E SE; Slattery, Matthew M
Publication Date: 2016-12

Variant appearance in text: rs369184
PubMed Link: 28203648
Variant Present in the following documents:
  • nihms825711.pdf
View BVdb publication page



A Polymorphic Antioxidant Response Element Links NRF2/sMAF Binding to Enhanced MAPT Expression and Reduced Risk of Parkinsonian Disorders.

Cell Reports
Wang, Xuting X; Campbell, Michelle R MR; Lacher, Sarah E SE; Cho, Hye-Youn HY; Wan, Ma M; Crowl, Christopher L CL; Chorley, Brian N BN; Bond, Gareth L GL; Kleeberger, Steven R SR; Slattery, Matthew M; Bell, Douglas A DA
Publication Date: 2016-04-26

Variant appearance in text: rs369184
PubMed Link: 27149848
Variant Present in the following documents:
  • Main text
View BVdb publication page



Removing reference mapping biases using limited or no genotype data identifies allelic differences in protein binding at disease-associated loci.

Bmc Medical Genomics
Buchkovich, Martin L ML; Eklund, Karl K; Duan, Qing Q; Li, Yun Y; Mohlke, Karen L KL; Furey, Terrence S TS
Publication Date: 2015-07-26

Variant appearance in text: rs369184
PubMed Link: 26210163
Variant Present in the following documents:
  • 12920_2015_Article_117.pdf
View BVdb publication page