MT-TR mitochondrially encoded tRNA arginine [Homo sapiens (human)] - Gene

Summary

Official Symbol: MT-TRprovided by HGNC
Official Full Name: mitochondrially encoded tRNA arginineprovided by HGNC
Primary source: HGNC:HGNC:7496
See related: MIM:590005; AllianceGenome:HGNC:7496
Gene type: tRNA
Organism: Homo sapiens
Lineage: Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as: MTTR; TRNR
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Annotation release	Status	Assembly	Chr	Location
RS_2023_10	current	GRCh38.p14 (GCF_000001405.40)	MT (non-nuclear)	NC_012920.1 (10405..10469)
105.20220307	previous assembly	GRCh37.p13 (GCF_000001405.25)	MT (non-nuclear)	NC_012920.1 (10405..10469)

Chromosome MT - NC_012920.1 Genomic Context describing neighboring genes

Genomic Sequence:

Go to nucleotide: Graphics FASTA GenBank

A novel mitochondrial tRNA Arg mutation resulting in an anticodon swap in a patient with mitochondrial encephalomyopathy.
Title: A novel mitochondrial tRNA Arg mutation resulting in an anticodon swap in a patient with mitochondrial encephalomyopathy.
Observational study of gene-disease association. (HuGE Navigator)
Title: MtSNPscore: a combined evidence approach for assessing cumulative impact of mitochondrial variations in disease.
Observational study of genotype prevalence. (HuGE Navigator)
Title: Molecular epidemiology of childhood mitochondrial encephalomyopathies in a Finnish population: sequence analysis of entire mtDNA of 17 children reveals heteroplasmic mutations in tRNAArg, tRNAGlu, and tRNALeu(UUR) genes.