Homo sapiens troponin C1, slow skeletal and cardiac type (TNNC1), mRNA

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A novel variant of TNNC1 associated with severe dilated cardiomyopathy causing infant mortality and stillbirth: a case of germline mosaicism. [J Genet. 2023]
A novel variant of TNNC1 associated with severe dilated cardiomyopathy causing infant mortality and stillbirth: a case of germline mosaicism.
Udani R, Schilter KF, Tyler RC, Smith BA, Wendtandrae JL, Kappes UP, Scharer G, Lehman A, Steinraths M, Reddi HV. J Genet. 2023; 102.
Troponin C-1 Activated by E2F1 Accelerates Gastric Cancer Progression via Regulating TGF-β/Smad Signaling. [Dig Dis Sci. 2022]
Troponin C-1 Activated by E2F1 Accelerates Gastric Cancer Progression via Regulating TGF-β/Smad Signaling.
Fang C, Zhang X, Li C, Liu F, Liu H. Dig Dis Sci. 2022 Sep; 67(9):4444-4457. Epub 2021 Nov 19.
De Novo Missense Mutations in TNNC1 and TNNI3 Causing Severe Infantile Cardiomyopathy Affect Myofilament Structure and Function and Are Modulated by Troponin Targeting Agents. [Int J Mol Sci. 2021]
De Novo Missense Mutations in TNNC1 and TNNI3 Causing Severe Infantile Cardiomyopathy Affect Myofilament Structure and Function and Are Modulated by Troponin Targeting Agents.
Hassoun R, Budde H, Mannherz HG, Lódi M, Fujita-Becker S, Laser KT, Gärtner A, Klingel K, Möhner D, Stehle R, et al. Int J Mol Sci. 2021 Sep 6; 22(17). Epub 2021 Sep 6.

RefSeq protein product
See the reference protein sequence for troponin C, slow skeletal and cardiac muscles (NP_003271.1).

Protein
Protein sequence from Nucleotide coding region
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Homo sapiens troponin C1, slow skeletal and cardiac type (TNNC1), mRNA
Homo sapiens troponin C1, slow skeletal and cardiac type (TNNC1), mRNA
gi|1653962401|ref|NM_003280.3|

Nucleotide

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Nucleotide