Homo sapiens myosin heavy chain 11 (MYH11), transcript variant SM1B, m - Nucleotide

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Genome-wide analysis identifies MYH11 compound heterozygous variants leading to visceral myopathy corresponding to late-onset form of megacystis-microcolon-intestinal hypoperistalsis syndrome. [Mol Genet Genomics. 2024]
Genome-wide analysis identifies MYH11 compound heterozygous variants leading to visceral myopathy corresponding to late-onset form of megacystis-microcolon-intestinal hypoperistalsis syndrome.
Billon C, Piccoli GB, de Sainte Agathe JM, Stoeva R, Derive N, Heidet L, Berrebi D, Bruneval P, Jeunemaitre X, Hureaux M. Mol Genet Genomics. 2024 Apr 16; 299(1):44. Epub 2024 Apr 16.
A harmful MYH11 variant detected in a family with thoracic aortic dissection and patent ductus arteriosus. [Forensic Sci Med Pathol. 2024]
A harmful MYH11 variant detected in a family with thoracic aortic dissection and patent ductus arteriosus.
Pan M, Tan X, Sun T, Zhu W, Liu H, Liu Q, Dong H. Forensic Sci Med Pathol. 2024 Mar; 20(1):212-218. Epub 2023 Jun 12.
TBK1 phosphorylation activates LIR-dependent degradation of the inflammation repressor TNIP1. [J Cell Biol. 2023]
TBK1 phosphorylation activates LIR-dependent degradation of the inflammation repressor TNIP1.
Zhou J, Rasmussen NL, Olsvik HL, Akimov V, Hu Z, Evjen G, Kaeser-Pebernard S, Sankar DS, Roubaty C, Verlhac P, et al. J Cell Biol. 2023 Feb 6; 222(2). Epub 2022 Dec 27.

RefSeq alternative splicing
See 6 reference mRNA sequence splice variants for the MYH11 gene.
RefSeq protein product
See the reference protein sequence for myosin-11 isoform SM1B (NP_001035203.1).

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Nucleotide