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基因注释:MYL3

官方信息

官方名称:myosin light chain 3

功能摘要:MYL3 encodes myosin light chain 3, an alkali light chain also referred to in the literature as both the ventricular isoform and the slow skeletal muscle isoform. Mutations in MYL3 have been identified as a cause of mid-left ventricular chamber type hypertrophic cardiomyopathy. [provided by RefSeq, Jul 2008].

作为靶基因的剪接因子
  • HNRNPA2B1 综合评分: 0.350 · 证据 2 条
  • PTBP1 综合评分: 0.300 · 证据 2 条
  • Tardbp 综合评分: 0.248 · 证据 1 条
  • U2af1 综合评分: 0.212 · 证据 1 条
  • RBM20 综合评分: 0.100 · 证据 2 条
关联疾病

该基因暂无关联疾病记录

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