DMWD (gene)

DMWD
Identifiers
Aliases	DMWD, D19S593E, DMR-N9, DMRN9, gene59, dystrophia myotonica, WD repeat containing, DM1 locus, WD repeat containing
External IDs	OMIM: 609857; MGI: 94907; HomoloGene: 22559; GeneCards: DMWD; OMA:DMWD - orthologs
Gene location (Human)
Chr.	Chromosome 19 (human)
End	45,792,845 bp
Gene location (Mouse)
Chr.	Chromosome 7 (mouse)
End	18,816,701 bp
RNA expression pattern
	Top expressed in
	apex of heart; ; popliteal artery; ; tibial arteries; ; right auricle of heart; ; right coronary artery; ; gastrocnemius muscle; ; right frontal lobe; ; body of uterus; ; Descending thoracic aorta; ; gastric mucosa;
	Top expressed in
	Rostral migratory stream; ; subiculum; ; granulocyte; ; dentate gyrus of hippocampal formation granule cell; ; epithelium of lens; ; superior frontal gyrus; ; otic vesicle; ; nucleus accumbens; ; retinal pigment epithelium; ; prefrontal cortex;
	More reference expression data
	; ;
	More reference expression data
Gene ontology
Molecular function	molecular function;
Cellular component	nucleus; dendrite; cell projection; perikaryon; cellular component;
Biological process	protein deubiquitination;
	Sources:Amigo / QuickGO
Orthologs
	1762
	13401
	ENSG00000185800
	ENSMUSG00000030410
	Q09019
	Q08274
	NM_004943
	NM_010058; NM_001374607
	NP_004934
	NP_034188; NP_001361536
	Wikidata
View/Edit Human	View/Edit Mouse

Dystrophia myotonica WD repeat-containing protein is a protein that in humans is encoded by the DMWD gene.