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🧬 基因注释:ACTA1

📝 官方信息

官方名称:actin alpha 1, skeletal muscle

功能摘要:The product encoded by this gene belongs to the actin family of proteins, which are highly conserved proteins that play a role in cell motility, structure and integrity. Alpha, beta and gamma actin isoforms have been identified, with alpha actins being a major constituent of the contractile apparatus, while beta and gamma actins are involved in the regulation of cell motility. This actin is an alpha actin that is found in skeletal muscle. Mutations in this gene cause a variety of myopathies, including nemaline myopathy, congenital myopathy with excess of thin myofilaments, congenital myopathy with cores, and congenital myopathy with fiber-type disproportion, diseases that lead to muscle fiber defects with manifestations such as hypotonia. [provided by RefSeq, Sep 2019].

🎯 作为靶基因的剪接因子
  • Tardbp 综合评分: 0.274 · 证据 1 条
  • Mbnl2 综合评分: 0.262 · 证据 1 条
  • Rbmx 综合评分: 0.198 · 证据 1 条
  • Rnps1 综合评分: 0.198 · 证据 1 条
  • ACIN1 综合评分: 0.150 · 证据 2 条
  • CPSF6 综合评分: 0.150 · 证据 2 条
  • U2af1 综合评分: 0.150 · 证据 1 条
  • EIF4A3 综合评分: 0.100 · 证据 2 条
  • Srsf7 综合评分: 0.100 · 证据 1 条
🏥 关联疾病

该基因暂无关联疾病记录

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