Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Bioss
{{$productOrderCtrl.translations['antibody.pdp.commerceCard.promotion.promotions']}}
{{$productOrderCtrl.translations['antibody.pdp.commerceCard.promotion.viewpromo']}}
{{$productOrderCtrl.translations['antibody.pdp.commerceCard.promotion.promocode']}}: {{promo.promoCode}} {{promo.promoDescription}}. {{$productOrderCtrl.translations['antibody.pdp.commerceCard.promotion.learnmore']}}
DMWD (DM1 Locus, WD Repeat Containing) is a Protein Coding gene. Diseases associated with DMWD include Myotonic Dystrophy 1 and Corticosteroid Allergy. An important paralog of this gene is WDR20. [GeneCards]
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
Protein Aliases: dystrophia myotonica linked gene, N9; Dystrophia myotonica WD repeat-containing protein; dystrophia myotonica, WD repeat containing; Dystrophia myotonica-containing WD repeat motif protein; Protein 59; Protein DMR-N9
Gene Aliases: D19S593E; DM9; DMR-N9; DMRN9; DMWD; gene59
UniProt ID: (Human) Q09019, (Mouse) Q08274
Entrez Gene ID: (Human) 1762, (Rat) 680252, (Mouse) 13401
If an Invitrogen™ antibody doesn't perform as described on our website or datasheet,we'll replace the product at no cost to you, or provide you with a credit for a future purchase.*
Learn moreGet expert recommendations for common problems or connect directly with an on staff expert for technical assistance related to applications, equipment and general product use.
Contact tech support