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Fetal anomalies v0.3229 GNAI1 Zornitza Stark Marked gene: GNAI1 as ready
Fetal anomalies v0.3229 GNAI1 Zornitza Stark Gene: gnai1 has been classified as Red List (Low Evidence).
Fetal anomalies v0.3229 GNAI1 Zornitza Stark Phenotypes for gene: GNAI1 were changed from GNAI1 syndrome to GNAI1 syndrome; Developmental delay, seizures, and hypotonia
Fetal anomalies v0.3228 GNAI1 Zornitza Stark Publications for gene: GNAI1 were set to
Fetal anomalies v0.3227 GNAI1 Zornitza Stark Mode of inheritance for gene: GNAI1 was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Fetal anomalies v0.3226 GNAI1 Zornitza Stark Classified gene: GNAI1 as Red List (low evidence)
Fetal anomalies v0.3226 GNAI1 Zornitza Stark Gene: gnai1 has been classified as Red List (Low Evidence).
Fetal anomalies v0.3225 GNAI1 Zornitza Stark changed review comment from: 7 de novo missense and 1 PTV variants reported in the DDD paper Table 1.; to: 7 de novo missense and 1 PTV variants reported in the DDD paper Table 1. Typically presents post-natally.
Fetal anomalies v0.3225 GNAI1 Zornitza Stark edited their review of gene: GNAI1: Changed rating: RED
Fetal anomalies v0.0 GNAI1 Zornitza Stark gene: GNAI1 was added
gene: GNAI1 was added to Fetal anomalies. Sources: Expert Review Amber,Genomics England PanelApp
Mode of inheritance for gene: GNAI1 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes for gene: GNAI1 were set to GNAI1 syndrome