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Pierre Robin Sequence v1.0 ALX4 Gene migrated from ENSG00000052850 to ENSG00000052850 (gene set migration)
Pierre Robin Sequence v0.21 ALX4 Zornitza Stark Phenotypes for gene: ALX4 were changed from to Frontonasal dysplasia 2, MIM# 613451; FND2 with alopecia
Pierre Robin Sequence v0.20 ALX4 Zornitza Stark Publications for gene: ALX4 were set to
Pierre Robin Sequence v0.19 ALX4 Zornitza Stark Mode of inheritance for gene: ALX4 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Pierre Robin Sequence v0.18 ALX4 Zornitza Stark reviewed gene: ALX4: Rating: AMBER; Mode of pathogenicity: None; Publications: ; Phenotypes: Frontonasal dysplasia 2, MIM# 613451; Mode of inheritance: None
Pierre Robin Sequence v0.18 ALX4 Tiong Tan Marked gene: ALX4 as ready
Pierre Robin Sequence v0.18 ALX4 Tiong Tan Gene: alx4 has been classified as Amber List (Moderate Evidence).
Pierre Robin Sequence v0.18 ALX4 Tiong Tan Classified gene: ALX4 as Amber List (moderate evidence)
Pierre Robin Sequence v0.18 ALX4 Tiong Tan Gene: alx4 has been classified as Amber List (Moderate Evidence).
Pierre Robin Sequence v0.17 ALX4 Tiong Tan reviewed gene: ALX4: Rating: AMBER; Mode of pathogenicity: None; Publications: 24668755, 22140057, 19692347; Phenotypes: FRONTONASAL DYSPLASIA 2, FND2 with alopecia; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Pierre Robin Sequence v0.0 ALX4 Zornitza Stark gene: ALX4 was added
gene: ALX4 was added to Pierre Robin sequence _VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services
Mode of inheritance for gene: ALX4 was set to Unknown