DMWD
Description
The DMWD (DM1 locus, WD repeat containing) is a protein-coding gene located on chromosome 19.
DMWD refers to Dystrophia myotonica WD repeat-containing protein.
DMWD is a regulator of the deubiquitinating USP12/DMWD/WDR48 complex. It acts as a cofactor that enhances the enzymatic activity of USP12.
DMWD is also known as D19S593E, DMR-N9, DMRN9, gene59.
