Lentiviral human ACTA1 sgRNA gene knockout kit

Human ACTA1

Gene symbol: ACTA1
Synonyms: ACTA ASMA CFTD CFTD1 CFTDM MPFD NEM1 NEM2 NEM3 SHPM
Species: HUMAN
Gene ID: 58
Summary: 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].
NM numbers targeted (Accession number:Exon:CDS Fragment): NM_001100:2:1