Homo sapiens troponin T1, slow skeletal type (TNNT1), RefSeqGene (LRG_ - Nucleotide

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Gene correction and overexpression of TNNI3 improve impaired relaxation in engineered heart tissue model of pediatric restrictive cardiomyopathy. [Dev Growth Differ. 2024]
Gene correction and overexpression of TNNI3 improve impaired relaxation in engineered heart tissue model of pediatric restrictive cardiomyopathy.
Hasegawa M, Miki K, Kawamura T, Takei Sasozaki I, Higashiyama Y, Tsuchida M, Kashino K, Taira M, Ito E, Takeda M, et al. Dev Growth Differ. 2024 Feb; 66(2):119-132. Epub 2024 Jan 9.
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.

RefSeq alternative splicing
See 10 reference mRNA sequence splice variants for the TNNT1 gene.

Protein
Protein sequence from Nucleotide coding region
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RNA
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Nucleotide