RecName: Full=Actin, alpha skeletal muscle; AltName: Full=Alpha-actin- - Protein

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A recurrent ACTA1 amino acid change in mosaic form causes milder asymmetric myopathy. [Neuromuscul Disord. 2024]
A recurrent ACTA1 amino acid change in mosaic form causes milder asymmetric myopathy.
Lehtokari VL, Sagath L, Davis M, Ho D, Kiiski K, Kettunen K, Demczko M, Stein R, Vatta M, Winder TL, et al. Neuromuscul Disord. 2024 Jan; 34:32-40. Epub 2023 Nov 30.
Morphological and functional alterations of neuromuscular synapses in a mouse model of ACTA1 congenital myopathy. [Hum Mol Genet. 2024]
Morphological and functional alterations of neuromuscular synapses in a mouse model of ACTA1 congenital myopathy.
Liu Y, Lin W. Hum Mol Genet. 2024 Jan 20; 33(3):233-244.
Novel p.Asp27Glu ACTA1 variant features congenital myopathy with finger flexor weakness, cardiomyopathy, and cardiac conduction defects. [Neuromuscul Disord. 2023]
Novel p.Asp27Glu ACTA1 variant features congenital myopathy with finger flexor weakness, cardiomyopathy, and cardiac conduction defects.
Mulvany-Robbins B, Putko B, Schmitt L, Oudit G, Phan C, Beecher G. Neuromuscul Disord. 2023 Jul; 33(7):546-550. Epub 2023 May 30.

RefSeq protein isoforms
See 2 reference sequence protein isoforms for the Acta1 gene.

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MODBASE, Database of Comparative Protein Structure Models (Sali Lab/UCSF) [MODBASE, Database of Comparat...]
MODBASE, Database of Comparative Protein Structure Models (Sali Lab/UCSF)
Mouse Genome Informatics (MGI) [Mouse Genome Informatics (MGI)]
Mouse Genome Informatics (MGI)
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reagents [ExactAntigen/Labome]
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ExactAntigen/Labome
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ExactAntigen/Labome

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Protein