Possible mitochondrial disorder - nuclear genes
Gene: SUCLG2

SUCLG2 (succinate-CoA ligase GDP-forming beta subunit)
EnsemblGeneIds (GRCh38): ENSG00000172340
EnsemblGeneIds (GRCh37): ENSG00000172340
OMIM: 603922, Gene2Phenotype
SUCLG2 is in 4 panels

2 reviews

Ivone Leong (Genomics England Curator)

Red List (low evidence)

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.
Created: 4 Feb 2019, 1:36 p.m.

Mode of inheritance
Unknown

Phenotypes
None

Created: 4 Feb 2019, 1:36 p.m.

Panel version: 0.5

Shamima Rahman (UCL Institute of Child Health)

I don't know

no mutation reports in literature; good candidate gene for mtDNA depletion syndrome
Created: 4 Feb 2016, 9:24 p.m.

Created: 4 Feb 2016, 9:24 p.m.

Panel version: Imported from Mitochondrial disorders panel version 0.16

Details

Mode of Inheritance

Unknown

Sources

NHS GMS
Expert Review Red

Phenotypes

None

OMIM

603922

Clinvar variants

Variants in SUCLG2

Penetrance

None

Panels with this gene

History Filter Activity

4 Feb 2019, Gel status: 1

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

Ivone Leong (Genomics England Curator)

gene: SUCLG2 was added gene: SUCLG2 was added to Possible mitochondrial disorder - nuclear genes. Sources: Expert Review Red,NHS GMS Mode of inheritance for gene: SUCLG2 was set to Unknown Phenotypes for gene: SUCLG2 were set to None

Possible mitochondrial disorder - nuclear genes Gene: SUCLG2