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Cerebral vascular malformations v0.27 PIK3CA Zornitza Stark Marked gene: PIK3CA as ready
Cerebral vascular malformations v0.27 PIK3CA Zornitza Stark Gene: pik3ca has been classified as Green List (High Evidence).
Cerebral vascular malformations v0.27 PIK3CA Zornitza Stark Phenotypes for gene: PIK3CA were changed from Megalencephaly-Capillary Malformation-Polymicrogyria Syndrome; Megalencephaly-capillary malformation-polymicrogyria syndrome, somatic; Megalencephaly-capillary malformation-polymicrogyria syndrome, somatic, 602501; Congenital Lipomatous Overgrowth, Vascular Malformations, and Epidermal Nevi; Cerebral Malformation Disorders to Cerebral cavernous malformations 4, MIM#619538
Cerebral vascular malformations v0.26 PIK3CA Zornitza Stark Publications for gene: PIK3CA were set to
Cerebral vascular malformations v0.25 PIK3CA Zornitza Stark Mode of inheritance for gene: PIK3CA was changed from to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Cerebral vascular malformations v0.24 PIK3CA Zornitza Stark Classified gene: PIK3CA as Green List (high evidence)
Cerebral vascular malformations v0.24 PIK3CA Zornitza Stark Gene: pik3ca has been classified as Green List (High Evidence).
Cerebral vascular malformations v0.23 PIK3CA Zornitza Stark Tag somatic tag was added to gene: PIK3CA.
Cerebral vascular malformations v0.23 PIK3CA Zornitza Stark reviewed gene: PIK3CA: Rating: GREEN; Mode of pathogenicity: None; Publications: 34496175; Phenotypes: Cerebral cavernous malformations 4, MIM#619538; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Cerebral vascular malformations v0.0 PIK3CA Zornitza Stark gene: PIK3CA was added
gene: PIK3CA was added to Cerebral vascular malformations. Sources: Expert Review Red,Genomics England PanelApp
Mode of inheritance for gene: PIK3CA was set to
Phenotypes for gene: PIK3CA were set to Megalencephaly-Capillary Malformation-Polymicrogyria Syndrome; Megalencephaly-capillary malformation-polymicrogyria syndrome, somatic; Megalencephaly-capillary malformation-polymicrogyria syndrome, somatic, 602501; Congenital Lipomatous Overgrowth, Vascular Malformations, and Epidermal Nevi; Cerebral Malformation Disorders