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  3. ATP5G2
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Mitochondrial disorder with complex V deficiency

Gene: ATP5G2

Amber List (moderate 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

5 reviews

Carl Fratter (Oxford University Hospitals NHS Trust)

I don't know

Updated information and Amber review collated by Carl Fratter May 2019 on behalf of GMS mitochondrial specialist test group: no reports of human disease; complex V subunit
Created: 10 May 2019, 12:10 p.m.

Mode of inheritance
Unknown

Phenotypes
No OMIM phenotype

Publications

  • none found

Created: 10 May 2019, 12:10 p.m.

Panel version: 0.22

Ivone Leong (Genomics England Curator)

Green List (high evidence)

ATP5G2 has a new gene name: ATP5MC2
Created: 4 Feb 2019, 11:54 a.m.
Initial gene list and info collated by Carl Fratter (Oxford University Hospitals NHS Trust) January 2019 on behalf of the GMS Mitochondrial specialist test group. Gene Symbol submitted: ATP5MC2; Suggested intial gene rating: Green.
Created: 4 Feb 2019, 10:48 a.m.

Mode of inheritance
Unknown

Phenotypes
No OMIM phenotype

Created: 4 Feb 2019, 10:48 a.m.

Panel version: 0.3

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.
Created: 21 Mar 2018, 1:02 p.m.

Panel version: Imported from Mitochondrial disorders panel version 1.66

Ellen McDonagh (Genomics England Curator)

Comment when marking as ready: This gene should remain Amber due to the overall review and evidence assessment from the GMS mitochondrial specialist test group, submitted by Carl Fratter.
Created: 10 May 2019, 12:37 p.m.
Comment on list classification: This gene has been demoted to Amber until further evidence is provided. This gene is currently Red on the Mitochondrial disorders panel (code 112, Version 1.132) - further evidence needs to be submitted to support promoting this gene family member to Green.
Created: 29 Mar 2019, 1:14 p.m.
Comment when marking as ready: Candidate gene - should be kept on red list.
Created: 26 Feb 2016, 1:34 p.m.
Created: 26 Feb 2016, 1:34 p.m.

Panel version: Imported from Mitochondrial disorders panel version 0.346

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.
Created: 3 Feb 2016, 6:04 p.m.

Panel version: Imported from Mitochondrial disorders panel version 0.16

Details

Mode of Inheritance
Unknown
Sources
  • Expert Review Amber
  • NHS GMS
Phenotypes
  • No OMIM phenotype
Tags
new-gene-name
OMIM
603193
Clinvar variants
Variants in ATP5G2
Penetrance
None
Panels with this gene

History Filter Activity

10 May 2019, Gel status: 2

Entity classified by Genomics England curator

Ellen McDonagh (Genomics England Curator)

Gene: atp5g2 has been classified as Amber List (Moderate Evidence).

29 Mar 2019, Gel status: 2

Entity classified by Genomics England curator

Ellen McDonagh (Genomics England Curator)

Gene: atp5g2 has been classified as Amber List (Moderate Evidence).

4 Feb 2019, Gel status: 4

Added Tag

Ivone Leong (Genomics England Curator)

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

4 Feb 2019, Gel status: 4

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

Ivone Leong (Genomics England Curator)

gene: ATP5G2 was added gene: ATP5G2 was added to Mitochondrial disorder with complex V deficiency. Sources: Expert Review Green,NHS GMS Mode of inheritance for gene: ATP5G2 was set to Unknown Phenotypes for gene: ATP5G2 were set to No OMIM phenotype