Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Immunogen sequence: MLLRGLMKS YFGGLLCVCW SPDGRYVVTG GEDDLVTVWS FTEGRVVARG HGHKSWVNAV AFDPYTTRAE EAATAAGADG ERSGEEEEEE PEAAGTGSAG GAPLSPLPKA GSITYRFGSA GQDTQFCLWD LTEDVLYPHP PLARTRTLPG TPGTTPPAAS SSRGGEPGPG PLPRSLSRSN SLPHPAGGGK AGGPGVAAEP GTPFSIGRFA TLTLQERRDR GAEKEHKRYH SLGNISRGGS GGSGSGGEKP SGPVPRSRLD PAKVLGTALC PRIHEVPLLE PLVCKKIAQE RLTVLLFLED CIITACQEGL ICTWARPGKA GISSQPGNSP SGTVV (1-334 aa encoded by BC019266)
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
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