PREDICTED: Homo sapiens troponin T1, slow skeletal type (TNNT1), trans - Nucleotide

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WiTNNess: An international natural history study of infantile-onset TNNT1 myopathy. [Ann Clin Transl Neurol. 2023]
WiTNNess: An international natural history study of infantile-onset TNNT1 myopathy.
Strauss KA, Carson VJ, Bolettieri E, Everett M, Bollinger A, Bowser LE, Beiler K, Young M, Edvardson S, Fraenkel N, et al. Ann Clin Transl Neurol. 2023 Nov; 10(11):1972-1984. Epub 2023 Aug 25.
Slow skeletal muscle troponin T acts as a potential prognostic biomarker and therapeutic target for hepatocellular carcinoma. [Gene. 2023]
Slow skeletal muscle troponin T acts as a potential prognostic biomarker and therapeutic target for hepatocellular carcinoma.
Huang SC, Huang CC, Ko CY, Huang CY, Liu CH, Lee YK, Chen TY, Hsueh CW, Tzou SJ, Tai MH, et al. Gene. 2023 May 20; 865:147331. Epub 2023 Mar 5.
Adult-onset nemaline myopathy due to a novel homozygous variant in the TNNT1 gene. [Muscle Nerve. 2022]
Adult-onset nemaline myopathy due to a novel homozygous variant in the TNNT1 gene.
Martín-Jiménez P, Fuenmayor-Fernández de la Hoz CP, Hernández-Laín A, Arteche-López A, Quesada-Espinosa JF, Voth AH, Vesperinas A, Olivé M, Domínguez-González C. Muscle Nerve. 2022 Oct; 66(4):E13-E15. Epub 2022 Jul 27.

RefSeq alternative splicing
See 10 reference mRNA sequence splice variants for the TNNT1 gene.
RefSeq protein product
See the reference protein sequence for troponin T, slow skeletal muscle isoform X2 (XP_054177879.1).

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Nucleotide