Genes in panel
STRs in panel
Prev Next

Mitochondrial disorders

Gene: ATP5G2

Red List (low evidence)

ATP5G2 (ATP synthase, H+ transporting, mitochondrial Fo complex subunit C2 (subunit 9))
EnsemblGeneIds (GRCh38): ENSG00000135390
EnsemblGeneIds (GRCh37): ENSG00000135390
OMIM: 603193, Gene2Phenotype
ATP5G2 is in 4 panels

3 reviews

Louise Daugherty (Genomics England Curator)

Added new-gene-name tag, new approved HGNC gene symbol is ATP5MC2
Created: 21 Mar 2018, 1:02 p.m.

Ellen McDonagh (Genomics England Curator)

Comment when marking as ready: Candidate gene - should be kept on red list.
Created: 26 Feb 2016, 1:34 p.m.

Shamima Rahman (UCL Institute of Child Health)

I don't know

no mutation reports in literature;
good candidate gene for mitochondrial complex V (ATP synthase) deficiency
Created: 3 Feb 2016, 6:04 p.m.


  • Expert Review Red
  • Radboud University Medical Center, Nijmegen
  • No OMIM phenotype
Clinvar variants
Variants in ATP5G2
Panels with this gene

History Filter Activity

26 Feb 2016, Gel status: 1

Gene classified by Genomics England curator

Ellen McDonagh (Genomics England Curator)

This gene has been classified as Red List (Low Evidence).

30 Jun 2015, Gel status: 1

Added New Source

Ellen McDonagh (Genomics England Curator)

ATP5G2 was added to All recognised syndromes and those with suggestive featurespanel. Sources: Radboud University Medical Center, Nijmegen