MT-TA

MT-TA
Identifiers
Aliases	MT-TA, TRNA
External IDs	OMIM: 590000; MGI: 102491; GeneCards: MT-TA; OMA:MT-TA - orthologs
Orthologs
	4553
	17726
	ENSG00000210127
	ENSMUSG00000064347
	n; a
	n/a
	n/a
	n/a
	n/a
	n/a
	Wikidata
View/Edit Human	View/Edit Mouse

Mitochondrially encoded tRNA alanine also known as MT-TA is a transfer RNA, which in humans is encoded by the mitochondrial MT-TA gene.^[3]

MT-TA is a small 69 nucleotide RNA (human mitochondrial map position 5587-5655) that transfers the amino acid alanine to a growing polypeptide chain at the ribosome site of protein synthesis during translation.

It has been reported that the 5650G-A mutation on MT-TA may cause muscular dystrophy.^[4]

References

^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
^ Anderson S, Bankier AT, Barrell BG, de Bruijn MH, Coulson AR, Drouin J, Eperon IC, Nierlich DP, Roe BA, Sanger F, Schreier PH, Smith AJ, Staden R, Young IG (April 1981). "Sequence and organization of the human mitochondrial genome". Nature. 290 (5806): 457–65. Bibcode:1981Natur.290..457A. doi:10.1038/290457a0. PMID 7219534. S2CID 4355527.
^ Horvath, R (2003). "A tRNAAla mutation causing mitochondrial myopathy clinically resembling myotonic dystrophy". Journal of Medical Genetics. 40 (10): 752–757. doi:10.1136/jmg.40.10.752. ISSN 1468-6244. PMC 1735288. PMID 14569122.

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[1] "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.

[2] "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.

[pmid7219534-3] Anderson S, Bankier AT, Barrell BG, de Bruijn MH, Coulson AR, Drouin J, Eperon IC, Nierlich DP, Roe BA, Sanger F, Schreier PH, Smith AJ, Staden R, Young IG (April 1981). "Sequence and organization of the human mitochondrial genome". Nature. 290 (5806): 457–65. Bibcode:1981Natur.290..457A. doi:10.1038/290457a0. PMID 7219534. S2CID 4355527.

[Horvath2003-4] Horvath, R (2003). "A tRNAAla mutation causing mitochondrial myopathy clinically resembling myotonic dystrophy". Journal of Medical Genetics. 40 (10): 752–757. doi:10.1136/jmg.40.10.752. ISSN 1468-6244. PMC 1735288. PMID 14569122.

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