AARS2 (alanyl-tRNA synthetase 2, mitochondrial)

2014-11-01  

Identity

HGNC
LOCATION
6p21.1
LOCUSID
ALIAS
AARSL,COXPD8,LKENP,MT-ALARS,MTALARS

Other Information

Locus ID:

NCBI: 57505
MIM: 612035
HGNC: 21022
Ensembl: ENSG00000124608

Variants:

dbSNP: 57505
ClinVar: 57505
TCGA: ENSG00000124608
COSMIC: AARS2

RNA/Proteins

Gene IDTranscript IDUniprot
ENSG00000124608ENST00000244571Q5JTZ9

Expression (GTEx)

0
5
10
15
20
25

Pathways

PathwaySourceExternal ID
Aminoacyl-tRNA biosynthesisKEGGko00970
Aminoacyl-tRNA biosynthesisKEGGhsa00970
Aminoacyl-tRNA biosynthesis, eukaryotesKEGGhsa_M00359
Aminoacyl-tRNA biosynthesis, eukaryotesKEGGM00359
Gene ExpressionREACTOMER-HSA-74160
tRNA AminoacylationREACTOMER-HSA-379724
Mitochondrial tRNA aminoacylationREACTOMER-HSA-379726

Protein levels (Protein atlas)

Not detected
Low
Medium
High

References

Pubmed IDYearTitleCitations
379906422023AARS2 as a novel biomarker for prognosis and its molecular characterization in pan-cancer.1
379906422023AARS2 as a novel biomarker for prognosis and its molecular characterization in pan-cancer.1
339721712021Phenotypic diversity of brain MRI patterns in mitochondrial aminoacyl-tRNA synthetase mutations.12
339721712021Phenotypic diversity of brain MRI patterns in mitochondrial aminoacyl-tRNA synthetase mutations.12
302850852019Instability of the mitochondrial alanyl-tRNA synthetase underlies fatal infantile-onset cardiomyopathy.13
307066992019AARS2 leukoencephalopathy: A new variant of mitochondrial encephalomyopathy.15
312809592019Novel alanyl-tRNA synthetase 2 (AARS2) homozygous mutation in a consanguineous Chinese family with premature ovarian insufficiency.6
302850852019Instability of the mitochondrial alanyl-tRNA synthetase underlies fatal infantile-onset cardiomyopathy.13
307066992019AARS2 leukoencephalopathy: A new variant of mitochondrial encephalomyopathy.15
312809592019Novel alanyl-tRNA synthetase 2 (AARS2) homozygous mutation in a consanguineous Chinese family with premature ovarian insufficiency.6
288206242018Retinopathy and optic atrophy: Expanding the phenotypic spectrum of pathogenic variants in the AARS2 gene.11
294407752018Genetic defects in mtDNA-encoded protein translation cause pediatric, mitochondrial cardiomyopathy with early-onset brain disease.14
297490552018AARS2-related ovarioleukodystrophy: Clinical and neuroimaging features of three new cases.12
288206242018Retinopathy and optic atrophy: Expanding the phenotypic spectrum of pathogenic variants in the AARS2 gene.11
294407752018Genetic defects in mtDNA-encoded protein translation cause pediatric, mitochondrial cardiomyopathy with early-onset brain disease.14

Citation

Dessen P

AARS2 (alanyl-tRNA synthetase 2, mitochondrial)

Atlas Genet Cytogenet Oncol Haematol. 2014-11-01

Online version: http://atlasgeneticsoncology.org/gene/60020/haematological-explorer/meetings/