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STRs in panel
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Inborn errors of metabolism

Gene: TDO2

Red List (low evidence)

TDO2 (tryptophan 2,3-dioxygenase)
EnsemblGeneIds (GRCh38): ENSG00000151790
EnsemblGeneIds (GRCh37): ENSG00000151790
OMIM: 191070, Gene2Phenotype
TDO2 is in 3 panels

1 review

Helen Brittain (Genomics England Curator)

Red List (low evidence)

No phenotype associated with this gene
Created: 23 Feb 2017, 5:16 p.m.

Mode of inheritance
Unknown

Phenotypes
No OMIM number

Publications

Details

Mode of Inheritance
Unknown
Sources
  • London North GLH
  • NHS GMS
  • Expert Review Red
Phenotypes
  • No OMIM number
  • Tryptophanaemia (Disorders of histidine, tryptophan or lysine metabolism)
OMIM
191070
Clinvar variants
Variants in TDO2
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 TDO2. Source London North GLH was added to TDO2.

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: TDO2 was added gene: TDO2 was added to Inborn errors of metabolism. Sources: Expert Review Red Mode of inheritance for gene: TDO2 was set to Unknown Publications for gene: TDO2 were set to 27604308 Phenotypes for gene: TDO2 were set to No OMIM number; Tryptophanaemia (Disorders of histidine, tryptophan or lysine metabolism)