1. Genes and Genomic Entities
  2. ATP5G2

ATP5G2

ATP synthase, H+ transporting, mitochondrial Fo complex subunit C2 (subunit 9)
OMIM: 603193, Gene2Phenotype

4 panels

Panel Reviews Mode of inheritance Details
4 panels
Amber ATP5G2 in Mitochondrial disorder with complex V deficiency


Level 2: Mitochondrial
Version 3.3
Latest signed off version: v3.0 (30 Apr 2025)

review Unknown
Sources
  • Expert Review Amber
  • NHS GMS
Phenotypes
  • No OMIM phenotype
Tags
  • new-gene-name
Red ATP5G2 in Likely inborn error of metabolism


Level 2: Metabolic
Version 8.91
Latest signed off version: v8.0 (30 Apr 2025)

Component of the following Super Panels:

  • Childhood onset leukodystrophy
  • Hypotonic infant
  • Paediatric disorders
  • Unexplained death in infancy and sudden unexplained death in childhood

    		•  review Unknown
    Sources
    • Expert Review Red
    Phenotypes
    • No OMIM phenotype
    Tags
    • new-gene-name
    Amber ATP5G2 in Possible mitochondrial disorder - nuclear genes


    Level 2: Mitochondrial
    Version 4.20
    Latest signed off version: v4.0 (30 Apr 2025)

    		review Unknown
    Sources
    • Expert Review Amber
    • NHS GMS
    Phenotypes
    • No OMIM phenotype
    Tags
    • new-gene-name
    Red ATP5G2 in Mitochondrial disorders


    Level 2: Mitochondrial
    Version 9.41
    Latest signed off version: v9.0 (30 Apr 2025)

    Component of the following Super Panels:

  • Childhood onset leukodystrophy

    		•  review Not set
    Sources
    • Expert Review Red
    • Radboud University Medical Center, Nijmegen
    Phenotypes
    • No OMIM phenotype
    Tags
    • new-gene-name