TNNI1

Troponin I type 1 (skeletal, slow)
Identifiers
Symbols	TNNI1 ; DKFZp451O223; TNN1
External IDs	Template:OMIM5 Template:MGI HomoloGene: 2462
Gene ontology Molecular function Template:GNF GO Template:GNF GO Cellular component Template:GNF GO Biological process Template:GNF GO
RNA expression pattern
File:PBB GE TNNI1 205177 at tn.png
More reference expression data
Orthologs
Template:GNF Ortholog box
Species	Human	Mouse
Entrez	n/a	n/a
Ensembl	n/a	n/a
UniProt	n/a	n/a
RefSeq (mRNA)	n/a	n/a
RefSeq (protein)	n/a	n/a
Location (UCSC)	n/a	n/a
PubMed search	n/a	n/a

Troponin I type 1 (skeletal, slow), also known as TNNI1, is a human gene.

Further reading

• Hunkeler NM, Kullman J, Murphy AM (1991). "Troponin I isoform expression in human heart". Circ. Res. 69 (5): 1409–14. PMID 1934363.CS1 maint: Multiple names: authors list (link)
• Bhavsar PK, Dhoot GK, Cumming DV; et al. (1992). "Developmental expression of troponin I isoforms in fetal human heart". FEBS Lett. 292 (1–2): 5–8. PMID 1959627.CS1 maint: Explicit use of et al. (link) CS1 maint: Multiple names: authors list (link)
• Suzuki H, Kawarabayasi Y, Kondo J; et al. (1990). "Structure and regulation of rat long-chain acyl-CoA synthetase". J. Biol. Chem. 265 (15): 8681–5. PMID 2341402.CS1 maint: Explicit use of et al. (link) CS1 maint: Multiple names: authors list (link)
• Wade R, Eddy R, Shows TB, Kedes L (1990). "cDNA sequence, tissue-specific expression, and chromosomal mapping of the human slow-twitch skeletal muscle isoform of troponin I.". Genomics. 7 (3): 346–57. PMID 2365354.CS1 maint: Multiple names: authors list (link)
• Maruyama K, Sugano S (1994). "Oligo-capping: a simple method to replace the cap structure of eukaryotic mRNAs with oligoribonucleotides". Gene. 138 (1–2): 171–4. PMID 8125298.
• Corin SJ, Juhasz O, Zhu L; et al. (1994). "Structure and expression of the human slow twitch skeletal muscle troponin I gene". J. Biol. Chem. 269 (14): 10651–9. PMID 8144655.CS1 maint: Explicit use of et al. (link) CS1 maint: Multiple names: authors list (link)
• Jha PK, Leavis PC, Sarkar S (1997). "Interaction of deletion mutants of troponins I and T: COOH-terminal truncation of troponin T abolishes troponin I binding and reduces Ca2+ sensitivity of the reconstituted regulatory system". Biochemistry. 35 (51): 16573–80. doi:10.1021/bi9622433. PMID 8987992.CS1 maint: Multiple names: authors list (link)
• Tiso N, Rampoldi L, Pallavicini A; et al. (1997). "Fine mapping of five human skeletal muscle genes: alpha-tropomyosin, beta-tropomyosin, troponin-I slow-twitch, troponin-I fast-twitch, and troponin-C fast". Biochem. Biophys. Res. Commun. 230 (2): 347–50. doi:10.1006/bbrc.1996.5958. PMID 9016781.CS1 maint: Explicit use of et al. (link) CS1 maint: Multiple names: authors list (link)
• Suzuki Y, Yoshitomo-Nakagawa K, Maruyama K; et al. (1997). "Construction and characterization of a full length-enriched and a 5'-end-enriched cDNA library". Gene. 200 (1–2): 149–56. PMID 9373149.CS1 maint: Explicit use of et al. (link) CS1 maint: Multiple names: authors list (link)
• Jha PK, Sarkar S (1998). "A recombinant monocysteine mutant (Ser to Cys-155) of fast skeletal troponin T: identification by cross-linking of a domain involved in a physiologically relevant interaction with troponins C and I.". Biochemistry. 37 (35): 12253–60. doi:10.1021/bi980025z. PMID 9724539.
• Hartley JL, Temple GF, Brasch MA (2001). "DNA cloning using in vitro site-specific recombination". Genome Res. 10 (11): 1788–95. PMID 11076863.CS1 maint: Multiple names: authors list (link)
• Wiemann S, Weil B, Wellenreuther R; et al. (2001). "Toward a catalog of human genes and proteins: sequencing and analysis of 500 novel complete protein coding human cDNAs". Genome Res. 11 (3): 422–35. doi:10.1101/gr.154701. PMID 11230166.CS1 maint: Explicit use of et al. (link) CS1 maint: Multiple names: authors list (link)
• Lindhout DA, Li MX, Schieve D, Sykes BD (2002). "Effects of T142 phosphorylation and mutation R145G on the interaction of the inhibitory region of human cardiac troponin I with the C-domain of human cardiac troponin C.". Biochemistry. 41 (23): 7267–74. PMID 12044157.CS1 maint: Multiple names: authors list (link)
• Strausberg RL, Feingold EA, Grouse LH; et al. (2003). "Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences". Proc. Natl. Acad. Sci. U.S.A. 99 (26): 16899–903. doi:10.1073/pnas.242603899. PMID 12477932.CS1 maint: Explicit use of et al. (link) CS1 maint: Multiple names: authors list (link)
• Westfall MV, Borton AR (2003). "Role of troponin I phosphorylation in protein kinase C-mediated enhanced contractile performance of rat myocytes". J. Biol. Chem. 278 (36): 33694–700. doi:10.1074/jbc.M305404200. PMID 12815045.
• Polly P, Haddadi LM, Issa LL; et al. (2003). "hMusTRD1alpha1 represses MEF2 activation of the troponin I slow enhancer". J. Biol. Chem. 278 (38): 36603–10. doi:10.1074/jbc.M212814200. PMID 12857748.CS1 maint: Explicit use of et al. (link) CS1 maint: Multiple names: authors list (link)
• Ota T, Suzuki Y, Nishikawa T; et al. (2004). "Complete sequencing and characterization of 21,243 full-length human cDNAs". Nat. Genet. 36 (1): 40–5. doi:10.1038/ng1285. PMID 14702039.CS1 maint: Explicit use of et al. (link) CS1 maint: Multiple names: authors list (link)
• Thijssen VL, Ausma J, Gorza L; et al. (2005). "Troponin I isoform expression in human and experimental atrial fibrillation". Circulation. 110 (7): 770–5. doi:10.1161/01.CIR.0000138849.03311.C6. PMID 15289369.CS1 maint: Explicit use of et al. (link) CS1 maint: Multiple names: authors list (link)
• Brobbey A, Ravakhah K (2004). "Elevated serum cardiac troponin I level in a patient after a grand mal seizure and with no evidence of cardiac disease". Am. J. Med. Sci. 328 (3): 189–91. PMID 15367881.
• Gerhard DS, Wagner L, Feingold EA; et al. (2004). "The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)". Genome Res. 14 (10B): 2121–7. doi:10.1101/gr.2596504. PMID 15489334.CS1 maint: Explicit use of et al. (link) CS1 maint: Multiple names: authors list (link)