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BabyScreen+ newborn screening v1.114 MYO7A Tommy Li Added phenotypes Usher syndrome, type 1B, MIM# 276900; Deafness, autosomal recessive 2, 600060 for gene: MYO7A
BabyScreen+ newborn screening v0.1710 MYO7A Zornitza Stark Tag deafness tag was added to gene: MYO7A.
BabyScreen+ newborn screening v0.412 MYO7A Zornitza Stark Marked gene: MYO7A as ready
BabyScreen+ newborn screening v0.412 MYO7A Zornitza Stark Gene: myo7a has been classified as Green List (High Evidence).
BabyScreen+ newborn screening v0.412 MYO7A Zornitza Stark Phenotypes for gene: MYO7A were changed from Usher syndrome to Deafness, autosomal recessive 2, 600060; Usher syndrome, type 1B, MIM# 276900
BabyScreen+ newborn screening v0.411 MYO7A Zornitza Stark reviewed gene: MYO7A: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Deafness, autosomal recessive 2, 600060, Usher syndrome, type 1B, MIM# 276900; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
BabyScreen+ newborn screening v0.274 MYO7A David Amor reviewed gene: MYO7A: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Usher syndrome, type 1B; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
BabyScreen+ newborn screening v0.0 MYO7A Zornitza Stark gene: MYO7A was added
gene: MYO7A was added to gNBS. Sources: BabySeq Category A gene,Expert Review Green
Mode of inheritance for gene: MYO7A was set to BIALLELIC, autosomal or pseudoautosomal
Phenotypes for gene: MYO7A were set to Usher syndrome