The EEF1A2 gene homepage

General information
Gene symbol EEF1A2
Gene name eukaryotic translation elongation factor 1 alpha 2
Chromosome 20
Chromosomal band q13.3
Imprinted Unknown
Genomic reference NG_034083.1
Transcript reference NM_001958.3
Exon/intron information NM_001958.3 exon/intron table
Associated with diseases DEE33, MRD38
Citation reference(s) -
Refseq URL Genomic reference sequence
Curators (1) Global Variome, with Curator vacancy
Total number of public variants reported 47
Unique public DNA variants reported 35
Individuals with public variants 10
Hidden variants 2
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 May 03, 2013
Date last updated February 26, 2024
Version EEF1A2:240226

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_001958.3.
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/EEF1A2
HGNC 3192
Entrez Gene 1917
PubMed articles EEF1A2
OMIM - Gene 602959
OMIM - Diseases DEE33 (encephalopathy, developmental and epileptic, type 33)
MRD38 (mental retardation, autosomal dominant, type 38 (MRD-38))
HGMD EEF1A2
GeneCards EEF1A2
GeneTests EEF1A2
Orphanet EEF1A2


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00006879 20 eukaryotic translation elongation factor 1 alpha 2 NM_001958.3 NP_001949.1 47


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