Activity

Filter

Cancel
Date Panel Item Activity
6 actions
Fetal anomalies v2.0 CC2D2A Gene migrated from ENSG00000048342 to ENSG00000048342 (gene set migration)
Fetal anomalies v0.380 CC2D2A Zornitza Stark Marked gene: CC2D2A as ready
Fetal anomalies v0.380 CC2D2A Zornitza Stark Gene: cc2d2a has been classified as Green List (High Evidence).
Fetal anomalies v0.380 CC2D2A Zornitza Stark Phenotypes for gene: CC2D2A were changed from MECKEL SYNDROME, TYPE 6; JOUBERT SYNDROME 9; COACH SYNDROME to Joubert syndrome 9, MIM# 612285; Meckel syndrome 6, MIM# 612284; COACH syndrome 2, MIM# 619111
Fetal anomalies v0.379 CC2D2A Zornitza Stark Publications for gene: CC2D2A were set to
Fetal anomalies v0.0 CC2D2A Zornitza Stark gene: CC2D2A was added
gene: CC2D2A was added to Fetal anomalies. Sources: Expert Review Green,Genomics England PanelApp
Mode of inheritance for gene: CC2D2A was set to BIALLELIC, autosomal or pseudoautosomal
Phenotypes for gene: CC2D2A were set to MECKEL SYNDROME, TYPE 6; JOUBERT SYNDROME 9; COACH SYNDROME