Health / Medical Topics |
EZH2 Gene Mutation
A molecular genetic abnormality that refers to the presence of a mutation in the histone methyltransferase gene EZH2. (NCI Thesaurus)
YOU MAY ALSO LIKE
![](/lib/px2x1.gif)
This gene plays a role in chromatin remodeling and transcriptional regulation.
![](/lib/px2x1.gif)
An azetidinone derivative and a cholesterol absorption inhibitor with lipid-lowering activity. Ezetimibe appears to interact physically with cholesterol transporters at the brush…
![](/lib/px2x1.gif)
A liposomal small-molecule glutathione analog inhibitor of glutathione S-transferase (GST) P1-1 with hematopoiesis-stimulating activity. After intracellular de-esterification, the active form of TLK199…
![](/lib/px2x1.gif)
Eyes absent homolog 1 (592 aa, ~65 kDa) is encoded by the human EYA1 gene. This protein may play a role in…
![](/lib/px2x1.gif)
A covering worn over one eye.
![](/lib/px2x1.gif)
A condition characterized by the formation of fatty deposits under the skin in the area of the eyelids. These well-demarcated growths, more…
![](/lib/px2x1.gif)