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Fetal anomalies v0.3777 SUCLG1 Zornitza Stark Marked gene: SUCLG1 as ready
Fetal anomalies v0.3777 SUCLG1 Zornitza Stark Gene: suclg1 has been classified as Green List (High Evidence).
Fetal anomalies v0.3777 SUCLG1 Zornitza Stark Phenotypes for gene: SUCLG1 were changed from FATAL INFANTILE LACTIC ACIDOSIS to Mitochondrial DNA depletion syndrome 9 (encephalomyopathic type with methylmalonic aciduria) MIM#245400
Fetal anomalies v0.3776 SUCLG1 Zornitza Stark Publications for gene: SUCLG1 were set to 21093335
Fetal anomalies v0.3722 SUCLG1 Ain Roesley reviewed gene: SUCLG1: Rating: AMBER; Mode of pathogenicity: None; Publications: 33230783, 28358460; Phenotypes: Mitochondrial DNA depletion syndrome 9 (encephalomyopathic type with methylmalonic aciduria) MIM#245400; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Current diagnostic: yes
Fetal anomalies v0.3722 SUCLG1 Chirag Patel reviewed gene: SUCLG1: Rating: GREEN; Mode of pathogenicity: None; Publications: PubMed: 17668387, 19526370, 20693550, 30470562; Phenotypes: Mitochondrial DNA depletion syndrome 9 (encephalomyopathic type with methylmalonic aciduria) , OMIM #245400; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Fetal anomalies v0.0 SUCLG1 Zornitza Stark gene: SUCLG1 was added
gene: SUCLG1 was added to Fetal anomalies. Sources: Expert Review Green,Genomics England PanelApp
Mode of inheritance for gene: SUCLG1 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: SUCLG1 were set to 21093335
Phenotypes for gene: SUCLG1 were set to FATAL INFANTILE LACTIC ACIDOSIS