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Pierre Robin Sequence v1.0 EDN1 Gene migrated from ENSG00000078401 to ENSG00000078401 (gene set migration)
Pierre Robin Sequence v0.28 EDN1 Zornitza Stark Marked gene: EDN1 as ready
Pierre Robin Sequence v0.28 EDN1 Zornitza Stark Gene: edn1 has been classified as Amber List (Moderate Evidence).
Pierre Robin Sequence v0.28 EDN1 Zornitza Stark Phenotypes for gene: EDN1 were changed from to Auriculocondylar syndrome 3, MIM# 615706
Pierre Robin Sequence v0.27 EDN1 Zornitza Stark Publications for gene: EDN1 were set to
Pierre Robin Sequence v0.26 EDN1 Zornitza Stark Mode of inheritance for gene: EDN1 was changed from BIALLELIC, autosomal or pseudoautosomal to BIALLELIC, autosomal or pseudoautosomal
Pierre Robin Sequence v0.25 EDN1 Zornitza Stark Mode of inheritance for gene: EDN1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Pierre Robin Sequence v0.25 EDN1 Zornitza Stark Classified gene: EDN1 as Amber List (moderate evidence)
Pierre Robin Sequence v0.25 EDN1 Zornitza Stark Gene: edn1 has been classified as Amber List (Moderate Evidence).
Pierre Robin Sequence v0.24 EDN1 Zornitza Stark reviewed gene: EDN1: Rating: AMBER; Mode of pathogenicity: None; Publications: 23315542, 23913798, 24268655; Phenotypes: Auriculocondylar syndrome 3, MIM# 615706; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Pierre Robin Sequence v0.0 EDN1 Zornitza Stark gene: EDN1 was added
gene: EDN1 was added to Pierre Robin sequence _VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services
Mode of inheritance for gene: EDN1 was set to Unknown