TIMM29

translocase of inner mitochondrial membrane 29
OMIM: 617380, Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels

Red TIMM29 in Mendeliome


Version 1.2511

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Red
  • Literature
Phenotypes
  • Sengers syndrome MONDO:0008922, TIMM29-related

Red TIMM29 in Mitochondrial disease


Level 2: Metabolic disorders
Version 0.973

Component of the following Super Panels:

  • Metabolic Disorders Superpanel
  • Progressive Neurological Conditions
  • review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Red
    • Literature
    Phenotypes
    • Sengers syndrome MONDO:0008922, TIMM29-related