Homo sapiens troponin I3, cardiac type (TNNI3), mRNA

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Homozygous TNNI3 frameshift variant in a consanguineous family with lethal infantile dilated cardiomyopathy. [Mol Genet Genomic Med. 2024]
Homozygous TNNI3 frameshift variant in a consanguineous family with lethal infantile dilated cardiomyopathy.
Kraoua L, Louati A, Ahmed SB, Abida N, Khemiri M, Menif K, Mrad R, Zaffran S, Jaouadi H. Mol Genet Genomic Med. 2024 Jun; 12(6):e2486.
Decreased intranuclear cardiac troponin I impairs cardiac autophagy through FOS/ATG5 in ageing hearts. [J Cell Mol Med. 2024]
Decreased intranuclear cardiac troponin I impairs cardiac autophagy through FOS/ATG5 in ageing hearts.
Liu RM, Huang S, Hu D, Liu L, Sun HC, Tian J, Pan B. J Cell Mol Med. 2024 May; 28(9):e18357.
Impaired Relaxation in Induced Pluripotent Stem Cell-Derived Cardiomyocytes with Pathogenic TNNI3 Mutation of Pediatric Restrictive Cardiomyopathy. [J Am Heart Assoc. 2024]
Impaired Relaxation in Induced Pluripotent Stem Cell-Derived Cardiomyocytes with Pathogenic TNNI3 Mutation of Pediatric Restrictive Cardiomyopathy.
Wang R, Hasegawa M, Suginobe H, Yoshihara C, Ishii Y, Ueyama A, Ueda K, Hashimoto K, Hirose M, Ishii R, et al. J Am Heart Assoc. 2024 Mar 19; 13(6):e032375. Epub 2024 Mar 18.

RefSeq protein product
See the reference protein sequence for troponin I, cardiac muscle (NP_000354.4).

Protein
Protein sequence from Nucleotide coding region
PubMed
PubMed articles cited by Nucleotide sequence record
Taxonomy
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