Genes in panel

Likely inborn error of metabolism - targeted testing not possible

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 for ATP5G2 is ATP5MC2
Created: 9 May 2019, 3:07 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.


Mode of Inheritance
  • Expert Review Red
  • No OMIM phenotype
Clinvar variants
Variants in ATP5G2
Panels with this gene

History Filter Activity

9 May 2019, Gel status: 1

Added Tag

Louise Daugherty (Genomics England Curator)

Tag new-gene-name tag was added to gene: ATP5G2.

8 Jan 2019, Gel status: 1

Panel promoted to version 1.0

Ellen McDonagh (Genomics England Curator)

Sarah Leigh: Associated with phenotype in O

16 Dec 2018, Gel status: 1

Created, Added New Source, Set mode of inheritance, Set Phenotypes

Ellen McDonagh (Genomics England Curator)

gene: ATP5G2 was added gene: ATP5G2 was added to Inborn errors of metabolism. Sources: Expert Review Red Mode of inheritance for gene: ATP5G2 was set to Unknown Phenotypes for gene: ATP5G2 were set to No OMIM phenotype