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BabyScreen+ newborn screening v1.114 CUL7 Tommy Li Added phenotypes 3-M syndrome 1, MIM# 273750 for gene: CUL7
BabyScreen+ newborn screening v0.787 CUL7 Zornitza Stark Marked gene: CUL7 as ready
BabyScreen+ newborn screening v0.787 CUL7 Zornitza Stark Gene: cul7 has been classified as Red List (Low Evidence).
BabyScreen+ newborn screening v0.787 CUL7 Zornitza Stark Phenotypes for gene: CUL7 were changed from 3-M syndrome to 3-M syndrome 1, MIM# 273750
BabyScreen+ newborn screening v0.786 CUL7 Zornitza Stark Classified gene: CUL7 as Red List (low evidence)
BabyScreen+ newborn screening v0.786 CUL7 Zornitza Stark Gene: cul7 has been classified as Red List (Low Evidence).
BabyScreen+ newborn screening v0.785 CUL7 Zornitza Stark reviewed gene: CUL7: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: 3-M syndrome 1, MIM# 273750; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
BabyScreen+ newborn screening v0.0 CUL7 Zornitza Stark gene: CUL7 was added
gene: CUL7 was added to gNBS. Sources: BabySeq Category A gene,Expert Review Green
Mode of inheritance for gene: CUL7 was set to BIALLELIC, autosomal or pseudoautosomal
Phenotypes for gene: CUL7 were set to 3-M syndrome