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Fetal anomalies v0.192 ASNS Zornitza Stark Publications for gene: ASNS were set to
Fetal anomalies v0.191 ASNS Zornitza Stark edited their review of gene: ASNS: Changed mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Fetal anomalies v0.191 ASNS Zornitza Stark edited their review of gene: ASNS: Changed publications: 24139043
Fetal anomalies v0.191 ASNS Zornitza Stark Marked gene: ASNS as ready
Fetal anomalies v0.191 ASNS Zornitza Stark Gene: asns has been classified as Green List (High Evidence).
Fetal anomalies v0.191 ASNS Zornitza Stark Phenotypes for gene: ASNS were changed from Asparagine synthetase deficiency 615574 to Asparagine synthetase deficiency, MIM#615574
Fetal anomalies v0.190 ASNS Zornitza Stark changed review comment from: Progressive neurometabolic disorder, with high mortality in infancy but severe intellectual disability in those surviving longer.; to: Progressive neurometabolic disorder, with high mortality in infancy but severe intellectual disability in those surviving longer.

Microcephaly is present antenatally.
Fetal anomalies v0.0 ASNS Zornitza Stark gene: ASNS was added
gene: ASNS was added to Fetal anomalies. Sources: Expert Review Green,Genomics England PanelApp
Mode of inheritance for gene: ASNS was set to BIALLELIC, autosomal or pseudoautosomal
Phenotypes for gene: ASNS were set to Asparagine synthetase deficiency 615574