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Fetal anomalies v0.1183 CD151 Zornitza Stark Marked gene: CD151 as ready
Fetal anomalies v0.1183 CD151 Zornitza Stark Gene: cd151 has been classified as Red List (Low Evidence).
Fetal anomalies v0.1183 CD151 Zornitza Stark Phenotypes for gene: CD151 were changed from NEPHROPATHY WITH PRETIBIAL EPIDERMOLYSIS BULLOSA AND DEAFNESS to Nephropathy with pretibial epidermolysis bullosa and deafness, MIM#609057
Fetal anomalies v0.1182 CD151 Zornitza Stark Publications for gene: CD151 were set to
Fetal anomalies v0.1181 CD151 Zornitza Stark Classified gene: CD151 as Red List (low evidence)
Fetal anomalies v0.1181 CD151 Zornitza Stark Gene: cd151 has been classified as Red List (Low Evidence).
Fetal anomalies v0.1180 CD151 Zornitza Stark reviewed gene: CD151: Rating: RED; Mode of pathogenicity: None; Publications: 15265795, 29138120; Phenotypes: Nephropathy with pretibial epidermolysis bullosa and deafness, MIM#609057; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Fetal anomalies v0.0 CD151 Zornitza Stark gene: CD151 was added
gene: CD151 was added to Fetal anomalies. Sources: Expert Review Amber,Genomics England PanelApp
Mode of inheritance for gene: CD151 was set to BIALLELIC, autosomal or pseudoautosomal
Phenotypes for gene: CD151 were set to NEPHROPATHY WITH PRETIBIAL EPIDERMOLYSIS BULLOSA AND DEAFNESS