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- Newborns main panel
- TXNRD2
- AAAS 1
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- SLC26A3 2
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- SLC35A2 1
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- SLC5A6 1
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- TRNT1 1
- TSC1 1
- TSC2 1
- TSR2 1
- TTR 1
- TXNRD2 1
- UBE2T 1
- USP18 1
- VKORC1 1
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- XRCC2 1
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- WFS1 1
Newborns main panel
Gene: TXNRD2 Amber List (moderate evidence)EnsemblGeneIds (GRCh38): ENSG00000184470
EnsemblGeneIds (GRCh37): ENSG00000184470
OMIM: 606448, Gene2Phenotype
TXNRD2 is in 2 panels
1 review
Mafalda Gomes (Genomics England Curator)
The mechanism of pathogenicity is loss-of-function (LOF).Created: 1 Jun 2023, 2:40 p.m. | Last Modified: 1 Jun 2023, 2:40 p.m.
Panel Version: 0.137
1 family pmid:24601690Created: 1 Jun 2023, 12:22 p.m. | Last Modified: 1 Jun 2023, 12:22 p.m.
Panel Version: 0.135
Last Modified: 1 Jun 2023, 12:22 p.m.
Panel version: 0.137
Details
- Mode of Inheritance
- BIALLELIC, autosomal or pseudoautosomal
- Sources
-
- Expert Review Amber
- Phenotypes
-
- Glucocorticoid deficiency 5
- OMIM
- 606448
- Clinvar variants
- Variants in TXNRD2
- Penetrance
- None
- Panels with this gene
History Filter Activity
Added New Source, Set Phenotypes, Status Update
Mafalda Gomes (Genomics England Curator)Source Expert Review Amber was added to TXNRD2. Added phenotypes Glucocorticoid deficiency 5 for gene: TXNRD2 Rating Changed from Green List (high evidence) to Amber List (moderate evidence)
Added New Source, Set Phenotypes, Status Update
Mafalda Gomes (Genomics England Curator)Source Expert Review Green was added to TXNRD2. Added phenotypes Glucocorticoid deficiency 5 for gene: TXNRD2 Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Set Phenotypes
Mafalda Gomes (Genomics England Curator)Phenotypes for gene: TXNRD2 were changed from ?Glucocorticoid deficiency 5; Glucocorticoid deficiency 5 to Glucocorticoid deficiency 5
Added New Source, Set Phenotypes, Status Update
Mafalda Gomes (Genomics England Curator)Source Expert Review Amber was added to TXNRD2. Added phenotypes Glucocorticoid deficiency 5 for gene: TXNRD2 Rating Changed from No List (delete) to Amber List (moderate evidence)
Set Phenotypes
Mafalda Gomes (Genomics England Curator)Added phenotypes ?Glucocorticoid deficiency 5 for gene: TXNRD2
Created, Added New Source, Set mode of inheritance
Mafalda Gomes (Genomics England Curator)gene: TXNRD2 was added gene: TXNRD2 was added to Newborns main panel. Sources: Expert Review Removed Mode of inheritance for gene: TXNRD2 was set to BIALLELIC, autosomal or pseudoautosomal