LARS2 (leucyl-tRNA synthetase 2, mitochondrial)

2009-06-01   Dessen P  

Identity

HGNC
LOCATION
3p21.31
LOCUSID
ALIAS
HLASA,LEURS,PRLTS4,mtLeuRS
FUSION GENES

Other Information

Locus ID:

NCBI: 23395
MIM: 604544
HGNC: 17095
Ensembl: ENSG00000011376

Variants:

dbSNP: 23395
ClinVar: 23395
TCGA: ENSG00000011376
COSMIC: LARS2

RNA/Proteins

Gene IDTranscript IDUniprot
ENSG00000011376ENST00000265537A0A499FJL2
ENSG00000011376ENST00000414984E9PHM2
ENSG00000011376ENST00000430399C9JYR8
ENSG00000011376ENST00000485461A0A2R8Y581
ENSG00000011376ENST00000642274Q15031
ENSG00000011376ENST00000645846Q15031
ENSG00000011376ENST00000650792Q15031
ENSG00000011376ENST00000651549A0A494C1E0
ENSG00000011376ENST00000652135A0A494C1K2

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
390521012024Exome sequencing reveals pathogenic mutations in the LARS2 and HSD17B4 genes associated with Perrault syndrome and D-bifunctional protein deficiency in Moroccan families.0
390521012024Exome sequencing reveals pathogenic mutations in the LARS2 and HSD17B4 genes associated with Perrault syndrome and D-bifunctional protein deficiency in Moroccan families.0
357508962023Neonatal lactic acidosis explained by LARS2 defect.0
364367982023Lin28a induced mitochondrial dysfunction in human granulosa cells via suppressing LARS2 expression.5
381860932023[Analysis of perrault syndrome caused by pathogenic variants in LARS2 and HARS2 genes].0
357508962023Neonatal lactic acidosis explained by LARS2 defect.0
364367982023Lin28a induced mitochondrial dysfunction in human granulosa cells via suppressing LARS2 expression.5
381860932023[Analysis of perrault syndrome caused by pathogenic variants in LARS2 and HARS2 genes].0
355858802022LARS2 Regulates Apoptosis via ROS-Mediated Mitochondrial Dysfunction and Endoplasmic Reticulum Stress in Ovarian Granulosa Cells.11
356593372022Leucine-tRNA-synthase-2-expressing B cells contribute to colorectal cancer immunoevasion.25
355858802022LARS2 Regulates Apoptosis via ROS-Mediated Mitochondrial Dysfunction and Endoplasmic Reticulum Stress in Ovarian Granulosa Cells.11
356593372022Leucine-tRNA-synthase-2-expressing B cells contribute to colorectal cancer immunoevasion.25
324423352020The expanding LARS2 phenotypic spectrum: HLASA, Perrault syndrome with leukodystrophy, and mitochondrial myopathy.12
324423352020The expanding LARS2 phenotypic spectrum: HLASA, Perrault syndrome with leukodystrophy, and mitochondrial myopathy.12
307373372019Biallelic variants in LARS2 and KARS cause deafness and (ovario)leukodystrophy.22

Citation

Dessen P

LARS2 (leucyl-tRNA synthetase 2, mitochondrial)

Atlas Genet Cytogenet Oncol Haematol. 2009-06-01

Online version: http://atlasgeneticsoncology.org/gene/50944/lars2-(leucyl-trna-synthetase-2-mitochondrial)