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Fetal anomalies v0.1837 GBA2 Zornitza Stark Marked gene: GBA2 as ready
Fetal anomalies v0.1837 GBA2 Zornitza Stark Gene: gba2 has been classified as Red List (Low Evidence).
Fetal anomalies v0.1837 GBA2 Zornitza Stark Phenotypes for gene: GBA2 were changed from AUTOSOMAL-RECESSIVE CEREBELLAR ATAXIA WITH SPASTICITY. to Spastic paraplegia 46, autosomal recessive, MIM#614409
Fetal anomalies v0.1836 GBA2 Zornitza Stark Classified gene: GBA2 as Red List (low evidence)
Fetal anomalies v0.1836 GBA2 Zornitza Stark Gene: gba2 has been classified as Red List (Low Evidence).
Fetal anomalies v0.1835 GBA Zornitza Stark Marked gene: GBA as ready
Fetal anomalies v0.1835 GBA Zornitza Stark Gene: gba has been classified as Green List (High Evidence).
Fetal anomalies v0.1835 GBA Zornitza Stark Publications for gene: GBA were set to 30712880
Fetal anomalies v0.1834 GBA Zornitza Stark edited their review of gene: GBA: Changed publications: 12838552
Fetal anomalies v0.1834 GBA Zornitza Stark Phenotypes for gene: GBA were changed from GAUCHER DISEASE TYPE 1; GAUCHER DISEASE TYPE 3C; GAUCHER DISEASE PERINATAL LETHAL; GAUCHER DISEASE TYPE 3; GAUCHER DISEASE TYPE 2; GAUCHER DISEASE to Gaucher disease, perinatal lethal, MIM# 608013
Fetal anomalies v0.1833 GBA Zornitza Stark Deleted their comment
Fetal anomalies v0.1833 GBA Zornitza Stark edited their review of gene: GBA: Added comment: Multiple reports of perinatal lethal cases. IUGR, hydrops, polyhydramnios, decreased fetal movements.; Changed rating: GREEN; Changed phenotypes: Gaucher disease, perinatal lethal, MIM# 608013
Fetal anomalies v0.0 GBA2 Zornitza Stark gene: GBA2 was added
gene: GBA2 was added to Fetal anomalies. Sources: Expert Review Green,Genomics England PanelApp
Mode of inheritance for gene: GBA2 was set to BIALLELIC, autosomal or pseudoautosomal
Phenotypes for gene: GBA2 were set to AUTOSOMAL-RECESSIVE CEREBELLAR ATAXIA WITH SPASTICITY.
Fetal anomalies v0.0 GBA Zornitza Stark gene: GBA was added
gene: GBA was added to Fetal anomalies. Sources: Expert Review Green,Genomics England PanelApp
Mode of inheritance for gene: GBA was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: GBA were set to 30712880
Phenotypes for gene: GBA were set to GAUCHER DISEASE TYPE 1; GAUCHER DISEASE TYPE 3C; GAUCHER DISEASE PERINATAL LETHAL; GAUCHER DISEASE TYPE 3; GAUCHER DISEASE TYPE 2; GAUCHER DISEASE