1. Genes and Genomic Entities
  2. TIMM22

TIMM22

translocase of inner mitochondrial membrane 22
OMIM: 607251, Gene2Phenotype

3 panels

Panel Reviews Mode of inheritance Details
3 panels
Amber TIMM22 in Possible mitochondrial disorder - nuclear genes


Level 2: Mitochondrial
Version 4.23
Latest signed off version: v4.0 (30 Apr 2025)

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Amber
  • NHS GMS
Phenotypes
  • No OMIM phenotype
Red TIMM22 in DDG2P


Version 6.447
Latest signed off version: v6.0 (30 Apr 2025)

Component of the following Super Panels:

  • Paediatric disorders

    		•  review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • DD-Gene2Phenotype
    • Expert Review Red
    Phenotypes
    • TIMM22-related combined oxidative phosphorylation deficiency
    • OMIM:618851.0
    Amber TIMM22 in Mitochondrial disorders


    Level 2: Mitochondrial
    Version 9.46
    Latest signed off version: v9.0 (30 Apr 2025)

    Component of the following Super Panels:

  • Childhood onset leukodystrophy

    		•  review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Amber
    • NHS GMS
    Phenotypes
    • No OMIM phenotype