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Fetal anomalies v0.3901 PTEN Zornitza Stark Marked gene: PTEN as ready
Fetal anomalies v0.3901 PTEN Zornitza Stark Gene: pten has been classified as Amber List (Moderate Evidence).
Fetal anomalies v0.3901 PTEN Zornitza Stark Phenotypes for gene: PTEN were changed from LHERMITTE-DUCLOS DISEASE; PROTEUS SYNDROME; COWDEN DISEASE; BANNAYAN-ZONANA SYNDROME; VACTERL ASSOCIATION WITH HYDROCEPHALUS; MACROCEPHALY/AUTISM SYNDROME to Macrocephaly/autism syndrome, MIM# 605309
Fetal anomalies v0.3900 PTEN Zornitza Stark Publications for gene: PTEN were set to
Fetal anomalies v0.3899 PTEN Zornitza Stark Mode of inheritance for gene: PTEN was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Fetal anomalies v0.3898 PTEN Zornitza Stark changed review comment from: More than 10 individuals reported with PMG.; to: More than 10 individuals reported with PMG, otherwise clinical presentation is generally post-natal.
Fetal anomalies v0.3898 PTEN Zornitza Stark edited their review of gene: PTEN: Changed rating: AMBER
Fetal anomalies v0.3898 PTEN Zornitza Stark Classified gene: PTEN as Amber List (moderate evidence)
Fetal anomalies v0.3898 PTEN Zornitza Stark Gene: pten has been classified as Amber List (Moderate Evidence).
Fetal anomalies v0.0 PTEN Zornitza Stark gene: PTEN was added
gene: PTEN was added to Fetal anomalies. Sources: Expert Review Red,Genomics England PanelApp
Mode of inheritance for gene: PTEN was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes for gene: PTEN were set to LHERMITTE-DUCLOS DISEASE; PROTEUS SYNDROME; COWDEN DISEASE; BANNAYAN-ZONANA SYNDROME; VACTERL ASSOCIATION WITH HYDROCEPHALUS; MACROCEPHALY/AUTISM SYNDROME