DMWD (gene)

Dystrophia myotonica WD repeat-containing protein is a protein that in humans is encoded by the DMWD gene.^[5][6]

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)[1] Band 19q13.32 Start 45,782,947 bp[1] End 45,792,845 bp[1]
Gene location (Mouse) Chr. Chromosome 7 (mouse)[2] Band 7 A3|7 9.46 cM Start 18,810,152 bp[2] End 18,816,701 bp[2]
RNA expression pattern Bgee Human Mouse (ortholog) 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 BioGPS 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 Species Human Mouse Entrez 1762 13401 Ensembl ENSG00000185800 ENSMUSG00000030410 UniProt Q09019 Q08274 RefSeq (mRNA) NM_004943 NM_010058 NM_001374607 RefSeq (protein) NP_004934 NP_034188 NP_001361536 Location (UCSC) Chr 19: 45.78 – 45.79 Mb Chr 7: 18.81 – 18.82 Mb PubMed search [3] [4]
Wikidata
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