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BabyScreen+ newborn screening v1.114 CDT1 Tommy Li Added phenotypes MONDO:0013431; Meier-Gorlin syndrome 4, MIM# 613804 for gene: CDT1
Publications for gene CDT1 were updated from 22333897; 21358632; 21358631; 33338304 to 22333897; 33338304; 21358632; 21358631
BabyScreen+ newborn screening v0.613 CDT1 Zornitza Stark Marked gene: CDT1 as ready
BabyScreen+ newborn screening v0.613 CDT1 Zornitza Stark Gene: cdt1 has been classified as Red List (Low Evidence).
BabyScreen+ newborn screening v0.613 CDT1 Zornitza Stark Classified gene: CDT1 as Red List (low evidence)
BabyScreen+ newborn screening v0.613 CDT1 Zornitza Stark Gene: cdt1 has been classified as Red List (Low Evidence).
BabyScreen+ newborn screening v0.612 CDT1 Zornitza Stark reviewed gene: CDT1: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Meier-Gorlin syndrome 4, MIM# 613804, MONDO:0013431; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
BabyScreen+ newborn screening v0.0 CDT1 Zornitza Stark gene: CDT1 was added
gene: CDT1 was added to gNBS. Sources: Expert Review Green,BabySeq Category C gene
Mode of inheritance for gene: CDT1 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: CDT1 were set to 22333897; 21358632; 21358631; 33338304
Phenotypes for gene: CDT1 were set to Meier-Gorlin syndrome 4, MIM# 613804; MONDO:0013431