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

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Troponin C gene mutations on cardiac muscle cell and skeletal Regulation: A comprehensive review. [Gene. 2024]
Troponin C gene mutations on cardiac muscle cell and skeletal Regulation: A comprehensive review.
Aborode AT, Olamilekan Adesola R, Idris I, Adio WS, Scott GY, Chakoma M, Oluwaseun AA, Onifade IA, Adeoye AF, Aluko BA, et al. Gene. 2024 Nov 15; 927:148651. Epub 2024 Jun 11.
K48- and K63-linked ubiquitin chain interactome reveals branch- and length-specific ubiquitin interactors. [Life Sci Alliance. 2024]
K48- and K63-linked ubiquitin chain interactome reveals branch- and length-specific ubiquitin interactors.
Waltho A, Popp O, Lenz C, Pluska L, Lambert M, Dötsch V, Mertins P, Sommer T. Life Sci Alliance. 2024 Aug; 7(8). Epub 2024 May 21.
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.

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
PubMed
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Taxonomy
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Annotated Genomic
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