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Fetal anomalies v0.1684 CCDC65 Zornitza Stark Marked gene: CCDC65 as ready
Fetal anomalies v0.1684 CCDC65 Zornitza Stark Gene: ccdc65 has been classified as Red List (Low Evidence).
Fetal anomalies v0.1684 CCDC65 Zornitza Stark Phenotypes for gene: CCDC65 were changed from PRIMARY CILIARY DYSKINESIA to Ciliary dyskinesia, primary, 27, MIM# 615504
Fetal anomalies v0.1683 CCDC65 Zornitza Stark Publications for gene: CCDC65 were set to 30166424
Fetal anomalies v0.1682 CCDC65 Zornitza Stark edited their review of gene: CCDC65: Changed rating: RED
Fetal anomalies v0.398 CDC6 Zornitza Stark Marked gene: CDC6 as ready
Fetal anomalies v0.398 CDC6 Zornitza Stark Gene: cdc6 has been classified as Red List (Low Evidence).
Fetal anomalies v0.398 CDC6 Zornitza Stark Phenotypes for gene: CDC6 were changed from MEIER-GORLIN SYNDROME 5 to Meier-Gorlin syndrome 5 (MIM#613805)
Fetal anomalies v0.397 CDC6 Zornitza Stark Publications for gene: CDC6 were set to
Fetal anomalies v0.396 CDC6 Zornitza Stark Classified gene: CDC6 as Red List (low evidence)
Fetal anomalies v0.396 CDC6 Zornitza Stark Gene: cdc6 has been classified as Red List (Low Evidence).
Fetal anomalies v0.0 CCDC65 Zornitza Stark gene: CCDC65 was added
gene: CCDC65 was added to Fetal anomalies. Sources: Expert Review Red,Genomics England PanelApp
Mode of inheritance for gene: CCDC65 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: CCDC65 were set to 30166424
Phenotypes for gene: CCDC65 were set to PRIMARY CILIARY DYSKINESIA
Fetal anomalies v0.0 CDC6 Zornitza Stark gene: CDC6 was added
gene: CDC6 was added to Fetal anomalies. Sources: Expert Review Green,Genomics England PanelApp
Mode of inheritance for gene: CDC6 was set to BIALLELIC, autosomal or pseudoautosomal
Phenotypes for gene: CDC6 were set to MEIER-GORLIN SYNDROME 5