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STRs in panel
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Inborn errors of metabolism

Gene: SUGCT

Red List (low evidence)

SUGCT (succinyl-CoA:glutarate-CoA transferase)
EnsemblGeneIds (GRCh38): ENSG00000175600
EnsemblGeneIds (GRCh37): ENSG00000175600
OMIM: 609187, Gene2Phenotype
SUGCT is in 2 panels

1 review

Helen Brittain (Genomics England Curator)

Red List (low evidence)

No clear phenotype associated with glutaric aciduria type 3. Many people remain asymptomatic
Created: 23 Feb 2017, 5:16 p.m.

Mode of inheritance
BIALLELIC, autosomal or pseudoautosomal

Phenotypes
Glutaric aciduria type III 231690

Publications

Details

Mode of Inheritance
BIALLELIC, autosomal or pseudoautosomal
Sources
  • London North GLH
  • NHS GMS
  • Expert Review Red
Phenotypes
  • Glutaric aciduria type III (Organic acidurias)
  • Glutaric aciduria type III 231690
OMIM
609187
Clinvar variants
Variants in SUGCT
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 SUGCT. Source London North GLH was added to SUGCT.

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 publications, Set Phenotypes

Ellen McDonagh (Genomics England Curator)

gene: SUGCT was added gene: SUGCT was added to Inborn errors of metabolism. Sources: Expert Review Red Mode of inheritance for gene: SUGCT was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: SUGCT were set to 27604308 Phenotypes for gene: SUGCT were set to Glutaric aciduria type III (Organic acidurias); Glutaric aciduria type III 231690