Activity

Filter

Cancel
Date Panel Item Activity
13 actions
Hydrops fetalis v0.290 SPTA1 Zornitza Stark Marked gene: SPTA1 as ready
Hydrops fetalis v0.290 SPTA1 Zornitza Stark Gene: spta1 has been classified as Green List (High Evidence).
Hydrops fetalis v0.290 SPTA1 Zornitza Stark Publications for gene: SPTA1 were set to 34132406; 35483216; 31333484; 29594000
Hydrops fetalis v0.289 SPTA1 Zornitza Stark Publications for gene: SPTA1 were set to 34132406
Hydrops fetalis v0.289 SPTA1 Zornitza Stark Mode of inheritance for gene: SPTA1 was changed from MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted to BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Hydrops fetalis v0.288 SPTA1 Zornitza Stark Classified gene: SPTA1 as Green List (high evidence)
Hydrops fetalis v0.288 SPTA1 Zornitza Stark Gene: spta1 has been classified as Green List (High Evidence).
Hydrops fetalis v0.287 SPTA1 Zornitza Stark reviewed gene: SPTA1: Rating: GREEN; Mode of pathogenicity: None; Publications: 35483216, 31333484, 29594000; Phenotypes: Spherocytosis type 3 #270970, Elliptocytosis-2 #130600, Pyropoikilocytosis #266140; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Hydrops fetalis v0.284 SPTA1 Di Milnes Deleted their comment
Hydrops fetalis v0.284 SPTA1 Di Milnes edited their review of gene: SPTA1: Added comment: single case fetus consanguineous parents
severe anaemia with NIHF
homozygous variant NM_003126.4:c.83G>A; Changed phenotypes: Spherocytosis type 3 #270970, Elliptocytosis-2 #130600, Pyropoikilocytosis #266140
Hydrops fetalis v0.284 SPTA1 Di Milnes reviewed gene: SPTA1: Rating: AMBER; Mode of pathogenicity: None; Publications: 34132406; Phenotypes: Spherocytosis type 3 #270970, Elliptocytosis-2 #130600, pyropoikilocytosis #266140; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Hydrops fetalis v0.284 SPTA1 Di Milnes Deleted their review
Hydrops fetalis v0.284 SPTA1 Di Milnes gene: SPTA1 was added
gene: SPTA1 was added to Hydrops fetalis. Sources: Literature
Mode of inheritance for gene: SPTA1 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Publications for gene: SPTA1 were set to 34132406
Phenotypes for gene: SPTA1 were set to Spherocytosis type 3 #270970; Elliptocytosis-2 #130600; pyropoikilocytosis #266140
Review for gene: SPTA1 was set to AMBER
Added comment: single case fetus consanguineous parents
severe anaemia with NIHF
homozygous variant NM_003126.4:c.83G>A
Sources: Literature