
MT-TQ RNA Gene - GeneCards
2024年12月25日 · MT-TQ (Mitochondrially Encoded TRNA-Gln (CAA/G)) is an RNA Gene, and is affiliated with the tRNA class. Diseases associated with MT-TQ include Myopathy and …
MT-TQ - Wikipedia
MT-TQ is a small 72 nucleotide RNA (human mitochondrial map position 4329-4400) that transfers the amino acid glutamine to a growing polypeptide chain at the ribosome site of …
MT-TQ mitochondrially encoded tRNA glutamine - NIH Genetic …
2024年12月10日 · Clinical resource with information about MT-TQ, MELAS syndrome, and available tests. There are links to practice guidelines and authoritative resources like …
经验分享:线粒体基因组变异解读_mtDNA - 搜狐
2021年11月13日 · 目标:基于线粒体基因组的独有特性以及线粒体转运RNA(mt-tRNA)的保守结构和功能特点,本研究根据我们实验室三十多年的临床经验,建立了mt-tRNA基因变异解读的 …
A novel pathogenic mitochondrial DNA variant m.4344T>C in
2024年5月10日 · The MT-TQ gene encodes the mitochondrial glutamine transfer RNA (tRNA Gln), which functions to recognize and bind to glutamine, and then transport it to the correct …
Interpretation of mitochondrial tRNA variants
2020年1月22日 · Proper interpretation of mt-tRNA variants is crucial for accurate clinical diagnosis and genetic counseling. Correlations with tissue distribution, heteroplasmy levels, predicted …
MT-TQ mitochondrially encoded tRNA glutamine [Homo sapiens …
2024年12月10日 · Data indicate that the 4329C> G point mutation in mitochondrial transfer RNA genes tRNA (Ile) and tRNA (Gln) probably contributed to the pathogenesis of hypertension, …
Mitochondrial tRNA glutamine variant in hypertrophic cardiomyopathy
2013年9月27日 · The mutational analysis of mtDNA genes revealed four variants. The m.4395A>G transition (C6G) in the MT-TQ gene, which altered an evolutionary conserved …
NC_012920.1(MT-TQ):m.4336T>C AND Sensorineural deafness …
2001年6月1日 · Finnila et al. (2001) analyzed 1 group including 480 controls and 575 patients with diseases manifesting in middle life, including diabetes, epilepsy, sensorineural hearing loss, …
Advances in mt-tRNA Mutation-Caused Mitochondrial Disease …
In this review, we deepen the knowledge in the current models for the most studied mt-tRNA mutation-caused mitochondrial diseases, MELAS (mitochondrial encephalomyopathy, lactic …
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