| Variant ID | 27107 |
|---|---|
| Entrez Gene ID | 1959 |
| Gene | EGR2 (GeneCards) |
| Location | hg19 10:64727828-64727828
hg38 10:62968068-62968068 |
| Disease | Asymptomatic |
| Method | Single cell Sequencing Cell cloning |
| Mutation(HGVS format) | NC_000010.10:g.64727828 C>T (Genome Assembly: GRCh37) |
| 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 |
| MAF in gnomAD genome (version 2.0.1) | 0 |
|---|---|
| EIGEN score | -0.042 |
| CADD Raw score (version 1.3) | 0.6752 (Deleterious) |
| FATHMM raw prediction score | 0.10726 (Tolerated) |
| Deleterious probability by DeFine | 0.5173 (Deleterious) |
| 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 ID | 29217587.03 (view all the variants in this individual) |
|---|---|
| Pubmed ID | 29217587 |
| Whose mosaic mutation | Normal |
| Phenotype | 1 |
| Disease | Asymptomatic |
| OMIM ID |