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Fetal anomalies v0.1786 SLC25A38 Zornitza Stark Phenotypes for gene: SLC25A38 were changed from Anemia, sideroblastic, 2, pyridoxine-refractory, MIM#205950 to Anaemia, sideroblastic, 2, pyridoxine-refractory, MIM#205950
Fetal anomalies v0.1785 SLC25A38 Zornitza Stark Publications for gene: SLC25A38 were set to 19412178; 31338833
Fetal anomalies v0.1784 SLC25A38 Zornitza Stark Classified gene: SLC25A38 as Amber List (moderate evidence)
Fetal anomalies v0.1784 SLC25A38 Zornitza Stark Gene: slc25a38 has been classified as Amber List (Moderate Evidence).
Fetal anomalies v0.1783 SLC25A38 Zornitza Stark reviewed gene: SLC25A38: Rating: AMBER; Mode of pathogenicity: None; Publications: 34298585; Phenotypes: Anaemia, sideroblastic, 2, pyridoxine-refractory, MIM#205950; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Fetal anomalies v0.1759 SLC25A38 Seb Lunke Marked gene: SLC25A38 as ready
Fetal anomalies v0.1759 SLC25A38 Seb Lunke Gene: slc25a38 has been classified as Red List (Low Evidence).
Fetal anomalies v0.1759 SLC25A38 Seb Lunke Phenotypes for gene: SLC25A38 were changed from ANEMIA, SIDEROBLASTIC, PYRIDOXINE-REFRACTORY, AUTOSOMAL RECESSIVE to Anemia, sideroblastic, 2, pyridoxine-refractory, MIM#205950
Fetal anomalies v0.1758 SLC25A38 Seb Lunke Publications for gene: SLC25A38 were set to
Fetal anomalies v0.1757 SLC25A38 Seb Lunke Classified gene: SLC25A38 as Red List (low evidence)
Fetal anomalies v0.1757 SLC25A38 Seb Lunke Added comment: Comment on list classification: Red for fetal anomalies panel as no conclusive detectable fetal presentation
Fetal anomalies v0.1757 SLC25A38 Seb Lunke Gene: slc25a38 has been classified as Red List (Low Evidence).
Fetal anomalies v0.1756 SLC25A38 Seb Lunke reviewed gene: SLC25A38: Rating: RED; Mode of pathogenicity: None; Publications: 19412178, 31338833; Phenotypes: Anemia, sideroblastic, 2, pyridoxine-refractory, MIM#205950; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Current diagnostic: yes
Fetal anomalies v0.0 SLC25A38 Zornitza Stark gene: SLC25A38 was added
gene: SLC25A38 was added to Fetal anomalies. Sources: Expert Review Green,Genomics England PanelApp
Mode of inheritance for gene: SLC25A38 was set to BIALLELIC, autosomal or pseudoautosomal
Phenotypes for gene: SLC25A38 were set to ANEMIA, SIDEROBLASTIC, PYRIDOXINE-REFRACTORY, AUTOSOMAL RECESSIVE