Overview

Variant ID 13948
Entrez Gene ID 1959
Gene EGR2 (GeneCards)
Location hg19 10:64743788-64743788
hg38 10:62984028-62984028
Disease Asymptomatic
Method HiSeq 2000
Mutation(HGVS format) NC_000010.10:g.64743788 G>A (Genome Assembly: GRCh37)

Other information

Exon or Intron NA
Position in protein NA
Amino acid changes in protein NA > NA
Position in cDNA NA
Changes in cDNA NA > NA
mRNA accession NA
mRNA length NA
Reference length 135534747

Annotations and predictions

MAF in gnomAD genome (version 2.0.1) 0
EIGEN score -0.1974
CADD Raw score (version 1.3) -0.038444 (Deleterious)
FATHMM raw prediction score 0.07939 (Tolerated)
Deleterious probability by DeFine 0.0714 (Neutral)
Entrez Gene ID 1959 (NCBI Gene)
Official Gene Symbol EGR2 (GeneCards)
Number of variants in EGR2 in this database 5 (view all the variants)
Full name early growth response 2
Band 10q21.3
Other IDs Vega: OTTHUMG00000018308
OMIM: 129010
HGNC: HGNC:3239
Ensembl: ENSG00000122877
Other names AT591, CMT1D, CMT4E, KROX20
Summary The protein encoded by this gene is a transcription factor with three tandem C2H2-type zinc fingers. Defects in this gene are associated with Charcot-Marie-Tooth disease type 1D (CMT1D), Charcot-Marie-Tooth disease type 4E (CMT4E), and with Dejerine-Sottas syndrome (DSS). Multiple transcript variants encoding two different isoforms have been found for this gene. [provided by RefSeq, Oct 2008]

Individual #1

Individual ID 29217584.04 (view all the variants in this individual)
Pubmed ID 29217584
Whose mosaic mutation Normal  
Phenotype 1  
Disease Asymptomatic
OMIM ID

Publication #1: 29217584

Pubmed ID 29217584
Title Aging and neurodegeneration are associated with increased mutations in single human neurons.
Journal Science
Publication date 2018.02
Disease Cockayne syndrome Xeroderma Pigmentosum
Number of cases Male cases: 3; Female cases: 6; cases of unknown sex: 15;