moesin isoform X3 [Homo sapiens]

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The role of moesin in diagnosing and assessing severity of lymphangioleiomyomatosis. [Respir Res. 2024]
The role of moesin in diagnosing and assessing severity of lymphangioleiomyomatosis.
Song X, Cai H, Peng W, Chen K, Abuduxukuer Z, Zeng Y, Zhu G, Lu C, Chen Y, Wang J, et al. Respir Res. 2024 Jan 25; 25(1):57. Epub 2024 Jan 25.
Two cases of pediatric primary immunodeficiency caused by a familial moesin(MSN)gene mutation. [Clin Immunol. 2024]
Two cases of pediatric primary immunodeficiency caused by a familial moesin(MSN)gene mutation.
Li M, Luo S, Zhuo Z, Shu M. Clin Immunol. 2024 Jan; 258:109858. Epub 2023 Dec 3.
Hemizygous nonsense variant in the moesin gene (MSN) leads to a new autoimmune phenotype of Immunodeficiency 50. [Front Immunol. 2022]
Hemizygous nonsense variant in the moesin gene (MSN) leads to a new autoimmune phenotype of Immunodeficiency 50.
Kovács AL, Kárteszi J, Prohászka Z, Kalmár T, Késmárky G, Koltai K, Nagy Z, Sebők J, Vas T, Molnár K, et al. Front Immunol. 2022; 13:919411. Epub 2022 Sep 1.

RefSeq genomic sequence
See the genomic reference sequence for the MSN gene (NG_012516.2).
RefSeq mRNA
See reference mRNA sequence for the MSN gene (XM_047442131.1).
RefSeq protein isoforms
See 9 reference sequence protein isoforms for the MSN gene.

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Protein