Activity

Filter

Cancel
Date Panel Item Activity
13 actions
Fetal anomalies v1.515 GSPT2 Zornitza Stark Phenotypes for gene: GSPT2 were changed from Intellectual disability MONDO:0001071, GSPT2-related to Neurodevelopmental disorder, MONDO:0700092, GSPT2-related
Fetal anomalies v1.514 GSPT2 Zornitza Stark Publications for gene: GSPT2 were set to 28414775
Fetal anomalies v1.513 GSPT2 Zornitza Stark Classified gene: GSPT2 as Green List (high evidence)
Fetal anomalies v1.513 GSPT2 Zornitza Stark Gene: gspt2 has been classified as Green List (High Evidence).
Fetal anomalies v1.512 GSPT2 Zornitza Stark edited their review of gene: GSPT2: Added comment: PMID 41420488: Six unrelated males reported with hemizygosity for variants in GSTP2 and neurodevelopmental disorder including intellectual disability, language impairment, autism, motor impairment, epilepsy, or abnormal fetal brain development. Variants were reported to be inherited from unaffected mothers. Functional evidence did support deleterious effects of the variants and gene knock-out.; Changed rating: GREEN; Changed publications: 28414775, 41420488; Changed phenotypes: Neurodevelopmental disorder, MONDO:0700092, GSPT2-related
Fetal anomalies v1.476 GSPT2 Lucy Spencer Phenotypes for gene: GSPT2 were changed from XL intellectual disability to Intellectual disability MONDO:0001071, GSPT2-related
Fetal anomalies v0.3250 GSPT2 Zornitza Stark Marked gene: GSPT2 as ready
Fetal anomalies v0.3250 GSPT2 Zornitza Stark Gene: gspt2 has been classified as Red List (Low Evidence).
Fetal anomalies v0.3250 GSPT2 Zornitza Stark Phenotypes for gene: GSPT2 were changed from XL INTELLECTUAL DISABILITY to XL intellectual disability
Fetal anomalies v0.3249 GSPT2 Zornitza Stark Publications for gene: GSPT2 were set to
Fetal anomalies v0.3248 GSPT2 Zornitza Stark Classified gene: GSPT2 as Red List (low evidence)
Fetal anomalies v0.3248 GSPT2 Zornitza Stark Gene: gspt2 has been classified as Red List (Low Evidence).
Fetal anomalies v0.0 GSPT2 Zornitza Stark gene: GSPT2 was added
gene: GSPT2 was added to Fetal anomalies. Sources: Expert Review Amber,Genomics England PanelApp
Mode of inheritance for gene: GSPT2 was set to X-LINKED: hemizygous mutation in males, biallelic mutations in females
Phenotypes for gene: GSPT2 were set to XL INTELLECTUAL DISABILITY