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Holoprosencephaly and septo-optic dysplasia v0.29 DLL1 Zornitza Stark Marked gene: DLL1 as ready
Holoprosencephaly and septo-optic dysplasia v0.29 DLL1 Zornitza Stark Gene: dll1 has been classified as Red List (Low Evidence).
Holoprosencephaly and septo-optic dysplasia v0.29 DLL1 Zornitza Stark Phenotypes for gene: DLL1 were changed from to Neurodevelopmental disorder with nonspecific brain abnormalities and with or without seizures, MIM# 618709
Holoprosencephaly and septo-optic dysplasia v0.28 DLL1 Zornitza Stark Publications for gene: DLL1 were set to
Holoprosencephaly and septo-optic dysplasia v0.27 DLL1 Zornitza Stark Mode of inheritance for gene: DLL1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Holoprosencephaly and septo-optic dysplasia v0.26 DLL1 Zornitza Stark Classified gene: DLL1 as Red List (low evidence)
Holoprosencephaly and septo-optic dysplasia v0.26 DLL1 Zornitza Stark Gene: dll1 has been classified as Red List (Low Evidence).
Holoprosencephaly and septo-optic dysplasia v0.25 DLL1 Zornitza Stark reviewed gene: DLL1: Rating: RED; Mode of pathogenicity: None; Publications: 31353024; Phenotypes: Neurodevelopmental disorder with nonspecific brain abnormalities and with or without seizures, MIM# 618709; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Holoprosencephaly and septo-optic dysplasia v0.0 DLL1 Zornitza Stark gene: DLL1 was added
gene: DLL1 was added to Holoprosencephaly and septo-optic dysplasia_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services
Mode of inheritance for gene: DLL1 was set to Unknown