Human mRNA fragment for myosin heavy chain

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Bi-allelic variants in MYH3 cause recessively-inherited arthrogryposis. [Clin Genet. 2024]
Bi-allelic variants in MYH3 cause recessively-inherited arthrogryposis.
Morali B, Miranda V, Raelson J, Grimard G, Glavas P, Audibert F, Dumont NA, Barone J, Bamshad M, Lemyre E, et al. Clin Genet. 2024 Oct; 106(4):483-487. Epub 2024 Jun 10.
Functional assessment of a novel biallelic MYH3 variation causing CPSKF1B (contractures, pterygia, and spondylocarpotarsal fusion syndrome1B). [Mol Genet Genomic Med. 2024]
Functional assessment of a novel biallelic MYH3 variation causing CPSKF1B (contractures, pterygia, and spondylocarpotarsal fusion syndrome1B).
He QB, Wu CH, Sun DL, Yuan JY, Hu HY, Yang K, Chen WQ, Yan YS, Yin GY, Zhang J, et al. Mol Genet Genomic Med. 2024 Mar; 12(3):e2401.
METTL3 achieves lipopolysaccharide-induced myocardial injury via m(6)A-dependent stabilization of Myh3 mRNA. [Biochim Biophys Acta Mol Cell ...]
METTL3 achieves lipopolysaccharide-induced myocardial injury via m(6)A-dependent stabilization of Myh3 mRNA.
Gong C, Wu J, Li H, Luo C, Ji G, Guan X, Liu J, Wang M. Biochim Biophys Acta Mol Cell Res. 2023 Oct; 1870(7):119503. Epub 2023 May 27.

RefSeq alternative splicing
See 6 reference mRNA sequence splice variants for the MYH3 gene.

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Nucleotide