Hereditary ataxia

Gene: EIF2B3

Green List (high evidence)

EIF2B3 (eukaryotic translation initiation factor 2B subunit gamma)
EnsemblGeneIds (GRCh38): ENSG00000070785
EnsemblGeneIds (GRCh37): ENSG00000070785
OMIM: 606273, Gene2Phenotype
EIF2B3 is in 10 panels

2 reviews

Damian Smedley (Genomics England Curator)

Comment on list classification: Evidence from expert reviewer and OMIM
Created: 4 Feb 2016, 2:07 p.m.

Jonathan Williams (Oxford Medical Genetics Laboratories, Oxford University Hospitals NHS Foundation Trust)

Green List (high evidence)

Fine. Evidence in lit. Not on our panel
Created: 24 Nov 2015, 4:57 p.m.

Mode of inheritance
BIALLELIC, autosomal or pseudoautosomal

Phenotypes
Childhood ataxia with central nervous system hypomyelination/vanishing white matter disease

Details

Mode of Inheritance
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Illumina TruGenome Clinical Sequencing Services
  • Emory Genetics Laboratory
Phenotypes
  • Childhood ataxia with central nervous system hypomyelination/vanishing white matter disease
OMIM
606273
Clinvar variants
Variants in EIF2B3
Penetrance
Complete
Panels with this gene

History Filter Activity

4 Feb 2016, Gel status: 4

Gene classified by Genomics England curator

Damian Smedley (Genomics England Curator)

This gene has been classified as Green List (High Evidence).

4 Feb 2016, Gel status: 4

Gene classified by Genomics England curator

Damian Smedley (Genomics England Curator)

This gene has been classified as Green List (High Evidence).

6 Jul 2015, Gel status: 2

Set Mode of Inheritance

Ellen McDonagh (Genomics England Curator)

Model of inheritance for gene EIF2B3 was changed to BIALLELIC, autosomal or pseudoautosomal

6 Jul 2015, Gel status: 2

Added New Source

Ellen McDonagh (Genomics England Curator)

EIF2B3 was added to Hereditary ataxiapanel. Sources: Emory Genetics Laboratory,Illumina TruGenome Clinical Sequencing Services

6 Jul 2015, Gel status: 1

Added New Source

Ellen McDonagh (Genomics England Curator)

EIF2B3 was added to Hereditary ataxiapanel. Sources: Emory Genetics Laboratory,Illumina TruGenome Clinical Sequencing Services