ATP5H

ATP synthase, H+ transporting, mitochondrial Fo complex subunit D
Gene2Phenotype

3 panels

Panel Reviews Mode of inheritance Details
3 panels
Red ATP5H in Mitochondrial disorder with complex V deficiency


Level 2: Mitochondrial
Version 3.7
Latest signed off version: v3.6 (12 Aug 2026)

review Unknown
Sources
  • Expert Review Red
  • NHS GMS
Phenotypes
  • No OMIM phenotype
Tags
  • new-gene-name
Red ATP5H in Possible mitochondrial disorder, nuclear genes


Level 2: Mitochondrial
Version 5.18
Latest signed off version: v5.17 (12 Aug 2026)

review Unknown
Sources
  • Expert Review Red
  • NHS GMS
Phenotypes
  • No OMIM phenotype
Tags
  • new-gene-name
Red ATP5H 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 Unknown
    Sources
    • Expert Review Red
    • NHS GMS
    Phenotypes
    • No OMIM phenotype
    Tags
    • new-gene-name