Activity

Filter

Cancel
Date Panel Item Activity
6 actions
Clefting disorders v0.98 ALX3 Zornitza Stark Phenotypes for gene: ALX3 were changed from FND1; Frontorhiny; FRONTONASAL DYSPLASIA 1 to Frontonasal dysplasia 1, MIM# 136760; Frontorhiny
Clefting disorders v0.97 ALX3 Zornitza Stark reviewed gene: ALX3: Rating: AMBER; Mode of pathogenicity: None; Publications: ; Phenotypes: Frontonasal dysplasia 1, MIM# 136760; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Clefting disorders v0.95 ALX3 Tiong Tan Marked gene: ALX3 as ready
Clefting disorders v0.95 ALX3 Tiong Tan Gene: alx3 has been classified as Amber List (Moderate Evidence).
Clefting disorders v0.95 ALX3 Tiong Tan reviewed gene: ALX3: Rating: AMBER; Mode of pathogenicity: None; Publications: 19409524, 29215096, 31914496; Phenotypes: Frontorhiny; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Clefting disorders v0.0 ALX3 Zornitza Stark gene: ALX3 was added
gene: ALX3 was added to Clefting_GEL. Sources: Expert Review Amber
Mode of inheritance for gene: ALX3 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: ALX3 were set to 19409524; 22106187; 19401770
Phenotypes for gene: ALX3 were set to FND1; Frontorhiny; FRONTONASAL DYSPLASIA 1