1. Genes and Genomic Entities
  2. EIF3A

EIF3A

eukaryotic translation initiation factor 3 subunit A
OMIM: 602039, Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels
Green EIF3A in DDG2P


Version 7.1
Latest signed off version: v7.0 (6 May 2026)

Component of the following Super Panels:

  • Paediatric disorders

    		•  review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
    Sources
    • DD-Gene2Phenotype
    • Expert Review Green
    Phenotypes
    • EIF3A-related neurodevelopmental disorder with cardiac anomalies and craniofacial dysmorphism
    • MONDO:0100038
    Tags
    • gene-checked
    Amber EIF3A in Paediatric disorders - additional genes


    Level 2: Developmental disorders
    Version 8.6
    Latest signed off version: v8.0 (6 May 2026)

    Component of the following Super Panels:

  • Paediatric disorders

    		•  review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Amber
    • Literature
    Phenotypes
    • syndromic disease, MONDO:0002254
    Tags
    • Q1_26_promote_green
    • gene-checked