myosin-10 isoform 2 [Homo sapiens]

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Heterozygous variants in MYH10 associated with neurodevelopmental disorders and congenital anomalies with evidence for primary cilia-dependent defects in Hedgehog signaling. [Genet Med. 2022]
Heterozygous variants in MYH10 associated with neurodevelopmental disorders and congenital anomalies with evidence for primary cilia-dependent defects in Hedgehog signaling.
Holtz AM, VanCoillie R, Vansickle EA, Carere DA, Withrow K, Torti E, Juusola J, Millan F, Person R, Guillen Sacoto MJ, et al. Genet Med. 2022 Oct; 24(10):2065-2078. Epub 2022 Aug 18.
Down-regulation of MYH10 driven by chromosome 17p13.1 deletion promotes hepatocellular carcinoma metastasis through activation of the EGFR pathway. [J Cell Mol Med. 2021]
Down-regulation of MYH10 driven by chromosome 17p13.1 deletion promotes hepatocellular carcinoma metastasis through activation of the EGFR pathway.
Jin Q, Cheng M, Xia X, Han Y, Zhang J, Cao P, Zhou G. J Cell Mol Med. 2021 Dec; 25(24):11142-11156. Epub 2021 Nov 4.
Myosin Heavy Chain 10 (MYH10) Gene Silencing Reduces Cell Migration and Invasion in the Glioma Cell Lines U251, T98G, and SHG44 by Inhibiting the Wnt/β-Catenin Pathway. [Med Sci Monit. 2018]
Myosin Heavy Chain 10 (MYH10) Gene Silencing Reduces Cell Migration and Invasion in the Glioma Cell Lines U251, T98G, and SHG44 by Inhibiting the Wnt/β-Catenin Pathway.
Wang Y, Yang Q, Cheng Y, Gao M, Kuang L, Wang C. Med Sci Monit. 2018 Dec 15; 24:9110-9119. Epub 2018 Dec 15.

RefSeq genomic sequence
See the genomic reference sequence for the MYH10 gene (NG_042305.2).
RefSeq mRNA
See reference mRNA sequence for the MYH10 gene (NM_005964.5).
RefSeq protein isoforms
See 4 reference sequence protein isoforms for the MYH10 gene.

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OncoMX cancer biomarker resource [OncoMX cancer biomarker resou...]
OncoMX cancer biomarker resource
Transcript/Protein Information [PANTHER Classification System]
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reagent reviews
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