troponin I3, cardiac type
آخر تحديث 18 Aug 2020
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ال TNNI3 gene provides instructions for making a protein called cardiac troponin I, which is found solely in the heart (cardiac) muscle. Cardiac troponin I is one of three proteins that make up the troponin protein complex in cardiac muscle cells. The troponin complex is associated with a structure called the sarcomere, which is the basic unit of muscle contraction. Sarcomeres are made up of thick and thin filaments. The overlapping thick and thin filaments attach (bind) to each other and release, which allows the filaments to move relative to one another so that muscles can contract. The troponin complex, along with calcium, helps regulate tensing (contraction) of cardiac muscle.
Normal function
ال TNNI3 gene provides instructions for making a protein called cardiac troponin I, which is found solely in the heart (cardiac) muscle. Cardiac troponin I is one of three proteins that make up the troponin protein complex in cardiac muscle cells. The troponin complex is associated with a structure called the sarcomere, which is the basic unit of muscle contraction. Sarcomeres are made up of thick and thin filaments. The overlapping thick and thin filaments attach (bind) to each other and release, which allows the filaments to move relative to one another so that muscles can contract. The troponin complex, along with calcium, helps regulate tensing (contraction) of cardiac muscle.
For the heart to beat normally, cardiac muscle must contract and relax in a coordinated way. Cardiac troponin I helps to coordinate contraction of the heart. When calcium levels are low, the troponin complex binds to the thin filament. This binding blocks the interaction between the thick and thin filaments that is needed for muscle contraction. An increase in calcium levels causes structural changes in another troponin complex protein called troponin C, which then triggers the troponin complex to detach from the thin filament, allowing the heart muscle to contract.
Conditions referring to this gene or chromosome
Other names
cardiac troponin I
cTnI
TNNI3_HUMAN
troponin I type 3 (cardiac)
troponin I, cardiac muscle
Related patient information and medicines

Patient information leaflet
إنزيمات القلب
إنزيمات القلب يكون substances released by the heart muscle when it is injured - for example, during a heart attack or a severe case of angina. A heart attack (myocardial infarction) can present i... The cardiac enzyme levels that are tested are called cardiac troponins. Normal (skeletal) muscle also produces troponins but troponins T and I are.

Patient information leaflet
النوبة القلبية
There are typical changes to... However, it is possible to have a heart attack without having these ECG changes. Blood tests. A blood test that measures a chemical called troponin is the usual test that confirms أ heart attack. An angiography of the coronary arteries may also be performed to find the blockage in the artery. Other tests may be done.

Patient information leaflet
ألم في الصدر
Based on what they find, he or she may advise you... Investigations for chest pain can include: An ECG (electrocardiogram or 'heart tracing') There are often typical changes to the normal pattern of the 'heart tracing' (electrocardiogram, or ECG) in a heart attack. Blood tests A blood test that measures a chemical called troponin is the usual test.

Patient information leaflet
هل يمكنني تناول البيوتين والكولاجين معًا؟
If you are due to have a blood test, tell your doctor or the lab staff that you are taking a biotin supplement. Important precautions Blood test interference Biotin can significantly interfere with laboratory blood tests, including thyroid function و heart attack markers (troponin), leading to dangerously incorrect results. You must stop taking.

Patient information leaflet
هل يمكنني تناول أتورفاستاتين والبيوتين معًا؟
Muscle pain or weakness - atorvastatin Contact your doctor immediately if you ... In rare cases, this can lead to serious kidney problems. Laboratory blood tests Biotin can significantly interfere with certain lab tests, including heart attack markers (troponin) and thyroid tests, leading to incorrect results. Stop taking biotin at least 72 hours.

Patient information leaflet
فشل الجهاز التنفسي
They may help to work out the cause and also to detect any factors that may be worsening the respiratory failure, such as a low blood haemoglobin level (anaemia). Troponin blood tests : these are used to determine if there has been recent heart injury - for example, a heart attack which may have caused the respiratory failure. Thyroid function.
قراءة إضافية ومراجع
- troponin I3, cardiac type; MedlinePlus, National Library of Medicine.
- Bashyam MD, Savithri GR, Kumar MS, Narasimhan C, Nallari P. Molecular genetics of familial hypertrophic cardiomyopathy (FHC). J Hum Genet. 2003;48(2):55-64. doi: 10.1007/s100380300007.
- Gomes AV, Liang J, Potter JD. Mutations in human cardiac troponin I that are associated with restrictive cardiomyopathy affect basal ATPase activity and the calcium sensitivity of force development. J Biol Chem. 2005 Sep 2;280(35):30909-15. doi: 10.1074/jbc.M500287200. Epub 2005 Jun 15.
- Gomes AV, Potter JD. Cellular and molecular aspects of familial hypertrophic cardiomyopathy caused by mutations in the cardiac troponin I gene. Mol Cell Biochem. 2004 Aug;263(1-2):99-114. doi: 10.1023/B:MCBI.0000041852.42291.aa.
- Kaski JP, Syrris P, Burch M, Tome-Esteban MT, Fenton M, Christiansen M, Andersen PS, Sebire N, Ashworth M, Deanfield JE, McKenna WJ, Elliott PM. Idiopathic restrictive cardiomyopathy in children is caused by mutations in cardiac sarcomere protein genes. Heart. 2008 Nov;94(11):1478-84. doi: 10.1136/hrt.2007.134684. Epub 2008 May 8.
- Keren A, Syrris P, McKenna WJ. Hypertrophic cardiomyopathy: the genetic determinants of clinical disease expression. Nat Clin Pract Cardiovasc Med. 2008 Mar;5(3):158-68. doi: 10.1038/ncpcardio1110. Epub 2008 Jan 29.
- Marston SB. How do mutations in contractile proteins cause the primary familial cardiomyopathies? J Cardiovasc Transl Res. 2011 Jun;4(3):245-55. doi: 10.1007/s12265-011-9266-2. Epub 2011 Mar 22.
- Sen-Chowdhry S, Syrris P, McKenna WJ. Genetics of restrictive cardiomyopathy. Heart Fail Clin. 2010 Apr;6(2):179-86. doi: 10.1016/j.hfc.2009.11.005.
- Willott RH, Gomes AV, Chang AN, Parvatiyar MS, Pinto JR, Potter JD. Mutations in Troponin that cause HCM, DCM AND RCM: what can we learn about thin filament function? J Mol Cell Cardiol. 2010 May;48(5):882-92. doi: 10.1016/j.yjmcc.2009.10.031. Epub 2009 Nov 12.
- Xu Q, Dewey S, Nguyen S, Gomes AV. Malignant and benign mutations in familial cardiomyopathies: insights into mutations linked to complex cardiovascular phenotypes. J Mol Cell Cardiol. 2010 May;48(5):899-909. doi: 10.1016/j.yjmcc.2010.03.005. Epub 2010 Mar 16.
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المقال متاح أيضًا باللغة الإنجليزية, الألمانية, إسبانية, الفرنسية, إيطالي, البرتغالية, الهندية, العبرية, العربية ,، و السويدية.
18 Aug 2020 | أحدث إصدار
1 Feb 2013 | نُشر في الأصل
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