Homo sapiens cDNA FLJ37111 fis, clone BRACE2021254, highly similar to - Nucleotide

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Dominant and recessive congenital myasthenic syndromes caused by SYT2 mutations. [Muscle Nerve. 2021]
Dominant and recessive congenital myasthenic syndromes caused by SYT2 mutations.
Maselli RA, Wei DT, Hodgson TS, Sampson JB, Vazquez J, Smith HL, Pytel P, Ferns M. Muscle Nerve. 2021 Aug; 64(2):219-224. Epub 2021 Jun 12.
Dual proteome-scale networks reveal cell-specific remodeling of the human interactome. [Cell. 2021]
Dual proteome-scale networks reveal cell-specific remodeling of the human interactome.
Huttlin EL, Bruckner RJ, Navarrete-Perea J, Cannon JR, Baltier K, Gebreab F, Gygi MP, Thornock A, Zarraga G, Tam S, et al. Cell. 2021 May 27; 184(11):3022-3040.e28. Epub 2021 May 6.
New recessive mutations in SYT2 causing severe presynaptic congenital myasthenic syndromes. [Neurol Genet. 2020]
New recessive mutations in SYT2 causing severe presynaptic congenital myasthenic syndromes.
Bauché S, Sureau A, Sternberg D, Rendu J, Buon C, Messéant J, Boëx M, Furling D, Fauré J, Latypova X, et al. Neurol Genet. 2020 Dec; 6(6):e534. Epub 2020 Dec 3.

RefSeq alternative splicing
See 14 reference mRNA sequence splice variants for the SYT2 gene.

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Nucleotide