靶标９�p style="text-indent: 2em;">DMWD

产品别名９�p style="text-indent: 2em;">D19S593E� DMR-N9� DMRN9� gene59� DMWD� DM1 locus, WD repeat containing� DM1 locus, WD repeat containing� dystrophia myotonica WD repeat-containing protein� dystrophia myotonica, WD repeat containing� dystrophia myotonica-containing WD repeat motif protein� protein 59� 强直性肌营养不良相关蛋白9�

背景信息９�div style="text-indent: 2em;">DMWD is a 674 amino acid protein containing five WD repeats. DMWD may play a role in the development of mental symptoms in severe cases of myotonic dystrophy, a chronic multisystemic disease characterized by wasting of the muscles, heart conduction defects, cataracts, endocrine changes and myotonia. The DMWD gene is located upstream of the DMPK gene and is prominently expressed in tissues affected in myotonic dystrophy patients. DMWD may also contribute to regulation in meiosis. DMWD is expressed in kidney and spleen, with strongest expression in brain, liver and testis. The gene encoding DMWD maps to human chromosome 19q13.32 and mouse chromosome 7 A3.