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STRs in panel
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Inborn errors of metabolism

Gene: SUCLG2

Red List (low evidence)

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

2 reviews

Arianna Tucci (Genomics England Curator)

Red List (low evidence)

Does not have a phenotype in OMIM or pubmed
Created: 23 Feb 2017, 5:16 p.m.

Mode of inheritance
Unknown

Phenotypes
Succinyl-CoA synthetase deficiency (Other metabolic disorders)

Publications

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.

Details

Mode of Inheritance
Unknown
Sources
  • London North GLH
  • NHS GMS
Phenotypes
  • Succinyl-CoA synthetase deficiency (Other metabolic disorders)
  • No OMIM phenotype
OMIM
603922
Clinvar variants
Variants in SUCLG2
Penetrance
None
Publications
Panels with this gene

History Filter Activity

13 Feb 2019, Gel status: 1

Added New Source, Added New Source

Ivone Leong (Genomics England Curator)

Source NHS GMS was added to SUCLG2. Source London North GLH was added to SUCLG2.

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

Set Phenotypes

Ellen McDonagh (Genomics England Curator)

Added phenotypes No OMIM phenotype for gene: SUCLG2

16 Dec 2018, Gel status: 1

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

Ellen McDonagh (Genomics England Curator)

gene: SUCLG2 was added gene: SUCLG2 was added to Inborn errors of metabolism. Sources: Expert Review Red Mode of inheritance for gene: SUCLG2 was set to Unknown Publications for gene: SUCLG2 were set to 27604308 Phenotypes for gene: SUCLG2 were set to Succinyl-CoA synthetase deficiency (Other metabolic disorders)