The WARS2 gene homepage

General information
Gene symbol WARS2
Gene name tryptophanyl tRNA synthetase 2, mitochondrial
Chromosome 1
Chromosomal band p12
Imprinted Unknown
Genomic reference NG_050658.1
Transcript reference NM_015836.3
Exon/intron information NM_015836.3 exon/intron table
Associated with diseases ID, NEMMLAS
Citation reference(s) -
Refseq URL Genomic reference sequence
Curators (1) Global Variome, with Curator vacancy
Total number of public variants reported 27
Unique public DNA variants reported 16
Individuals with public variants 12
Hidden variants 0
Download all this gene's data Download all data
Notes Establishment of this gene variant database (LSDB) was supported by the Leiden University Medical Center (LUMC), Leiden, Nederland.
Date created September 13, 2012
Date last updated September 17, 2021
Version WARS2:210917

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_015836.3.
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
Homepage URL https://www.LOVD.nl/WARS2
HGNC 12730
Entrez Gene 10352
PubMed articles WARS2
OMIM - Gene 604733
OMIM - Diseases NEMMLAS (neurodevelopmental disorder, mitochondrial, with abnormal movements and lactic acidosis, with/without seizures (NEMMLAS))
HGMD WARS2
GeneCards WARS2
GeneTests WARS2
Orphanet WARS2


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00001006 1 transcript variant 1 NM_015836.3 NP_056651.1 27


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