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 5.18
Latest signed off version: v5.17 (12 Aug 2026)

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


Version 8.1
Latest signed off version: v8.0 (12 Aug 2026)

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 10.19
    Latest signed off version: v10.18 (12 Aug 2026)

    Component of the following Super Panels:

  • Leukodystrophy, childhood onset

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