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 6.424
Latest signed off version: v6.0 (30 Apr 2025)

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
    Amber EIF3A in Paediatric disorders - additional genes


    Level 2: Developmental disorders
    Version 7.31
    Latest signed off version: v7.0 (30 Apr 2025)

    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