1. Genes and Genomic Entities
  2. TIMM22

TIMM22

translocase of inner mitochondrial membrane 22
OMIM: 607251, Gene2Phenotype

2 panels

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


Version 3.106
Latest signed off version: v3.105 (1 May 2024)

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

Level 3: Mitochondrial
Level 2: Metabolic disorders
Version 6.4
Latest signed off version: v6.0 (1 May 2024)

Component of the following Super Panels:

  • Childhood onset leukodystrophy

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