COA4

cytochrome c oxidase assembly factor 4 homolog
OMIM: 608016, Gene2Phenotype

3 panels

Panel Reviews Mode of inheritance Details
3 panels
Red COA4 in Mitochondrial disorder with complex IV deficiency


Version 3.21
Latest signed off version: v3.20 (1 May 2024)

review Unknown
Sources
  • Expert Review Red
  • NHS GMS
Phenotypes
  • No OMIM phenotype
Red COA4 in Possible mitochondrial disorder - nuclear genes


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

review Unknown
Sources
  • Expert Review Red
  • NHS GMS
Phenotypes
  • No OMIM phenotype
Red COA4 in Mitochondrial disorders

Level 3: Mitochondrial
Level 2: Metabolic disorders
Version 6.1
Latest signed off version: v6.0 (1 May 2024)

Component of the following Super Panels:

  • Childhood onset leukodystrophy
  • review Unknown
    Sources
    • Expert Review Red
    • NHS GMS
    Phenotypes
    • No OMIM phenotype