RARA c.1196A>G ;(p.K399R)

Variant ID: 17-38512285-A-G

NM_000964.3(RARA):c.1196A>G;(p.K399R)

This variant was identified in 3 publications

View GRCh38 version.




Publications:


Retinoid receptor turnover mediated by sumoylation, ubiquitination and the valosin-containing protein is disrupted in glioblastoma.

Scientific Reports
Rodriguez, Virginia V; Bailey, Rolanda R; Larion, Mioara M; Gilbert, Mark R MR
Publication Date: 2019-11-07

Variant appearance in text: RARA: K399R
PubMed Link: 31700049
Variant Present in the following documents:
  • Main text
  • 41598_2019_Article_52696.pdf
  • 41598_2019_52696_MOESM1_ESM.pdf
View BVdb publication page



Systematic Analysis of the Genetic Variability That Impacts SUMO Conjugation and Their Involvement in Human Diseases.

Scientific Reports
Xu, Hao-Dong HD; Shi, Shao-Ping SP; Chen, Xiang X; Qiu, Jian-Ding JD
Publication Date: 2015-07-08

Variant appearance in text: RARA: Lys399Arg
PubMed Link: 26154679
Variant Present in the following documents:
  • srep10900.pdf
View BVdb publication page



Small ubiquitin-like modifier-2 modification of retinoic acid receptor-alpha regulates its subcellular localization and transcriptional activity.

Endocrinology
Zhu, Li L; Santos, Nadine C NC; Kim, Kwan Hee KH
Publication Date: 2009-12

Variant appearance in text: RARA: K399R
PubMed Link: 19850744
Variant Present in the following documents:
  • Main text
View BVdb publication page