Date | Panel | Item | Activity | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Aminoacidopathy v1.100 | TDO2 | Zornitza Stark Marked gene: TDO2 as ready | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Aminoacidopathy v1.100 | TDO2 | Zornitza Stark Gene: tdo2 has been classified as Red List (Low Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Aminoacidopathy v1.100 | TDO2 | Zornitza Stark Classified gene: TDO2 as Red List (low evidence) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Aminoacidopathy v1.100 | TDO2 | Zornitza Stark Gene: tdo2 has been classified as Red List (Low Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Aminoacidopathy v1.95 | TDO2 |
Sangavi Sivagnanasundram gene: TDO2 was added gene: TDO2 was added to Aminoacidopathy. Sources: ClinGen Mode of inheritance for gene: TDO2 was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: TDO2 were set to 28285122 Phenotypes for gene: TDO2 were set to familial hypertryptophanemia MONDO:0010907 Review for gene: TDO2 was set to RED Added comment: Reported in one individual to date however there is evidence that this is a benign biochemical variant with no clinical significance. Classified Limitied by Aminoacidopathy GCEP on 17/11/2023 - https://search.clinicalgenome.org/CCID:006345 Sources: ClinGen |