MARS2 gene homepage

General information
Gene symbol MARS2
Gene name methionyl-tRNA synthetase 2, mitochondrial
Chromosome 2
Chromosomal band q33.1
Imprinted Unknown
Genomic reference NC_000002.11
Transcript reference NM_138395.3
Exon/intron information NM_138395.3 exon/intron table
Associated with diseases COXPD-25, SPAX-3
Citation reference(s) -
Refseq URL Genomic reference sequence
Curators (1) LOVD-team, but with Curator vacancy
Total number of public variants reported 12
Unique public DNA variants reported 12
Individuals with public variants 4
Hidden variants 0
Date created May 03, 2013
Date last updated June 24, 2020
Version MARS2:200624

Graphical displays and utilities
Graphs Graphs displaying summary information of all variants in the database »
Reading frame checker The Reading-frame checker generates a prediction of the effect of whole-exon changes. Active for: NM_138395.3.
UCSC Genome Browser Show variants in the UCSC Genome Browser (full view, compact view)
Ensembl Genome Browser Show variants in the Ensembl Genome Browser (full view, compact view)
NCBI Sequence Viewer Show distribution histogram of variants in the NCBI Sequence Viewer

Links to other resources
HGNC 25133
Entrez Gene 92935
PubMed articles MARS2
OMIM - Gene 609728
OMIM - Diseases COXPD-25 (oxidative phosphorylation deficiency?, combined, type 25 (COXPD-25))
SPAX-3 (ataxia, spastic, type 3, autosomal dominant (SPAX-3))

Active transcripts




NCBI ID     

NCBI Protein ID     

00011828 2 methionyl-tRNA synthetase 2, mitochondrial NM_138395.3 NP_612404.1 12

Copyright & disclaimer
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