PPARG c.820G>C ;(p.E274Q)

Variant ID: 3-12458293-G-C

NM_138711.3(PPARG):c.820G>C;(p.E274Q)

This variant was identified in 3 publications

View GRCh38 version.




Publications:


COUP-TFII in Health and Disease.

Cells
Polvani, Simone S; Pepe, Sara S; Milani, Stefano S; Galli, Andrea A
Publication Date: 2019-12-31

Variant appearance in text: PPARgamma: E276Q
PubMed Link: 31906104
Variant Present in the following documents:
  • Main text
  • cells-09-00101.pdf
View BVdb publication page



Transcriptional Factors Mediating Retinoic Acid Signals in the Control of Energy Metabolism.

International Journal Of Molecular Sciences
Zhang, Rui R; Wang, Yueqiao Y; Li, Rui R; Chen, Guoxun G
Publication Date: 2015-06-23

Variant appearance in text: NR1C3: E276Q
PubMed Link: 26110391
Variant Present in the following documents:
  • Main text
  • ijms-16-14210.pdf
View BVdb publication page



A Novel ESRRB Deletion Is a Rare Cause of Autosomal Recessive Nonsyndromic Hearing Impairment among Pakistani Families.

Genetics Research International
Lee, Kwanghyuk K; Khan, Saadullah S; Ansar, Muhammad M; Santos-Cortez, Regie Lyn P RL; Ahmad, Wasim W; Leal, Suzanne M SM
Publication Date: 2011

Variant appearance in text: PPARG: E276Q
PubMed Link: 22567352
Variant Present in the following documents:
  • Main text
  • GRI2011-368915.pdf
View BVdb publication page