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BabyScreen+ newborn screening v1.114 LITAF Tommy Li Added phenotypes Charcot-Marie-Tooth disease, type 1C, MIM# 601098 for gene: LITAF
BabyScreen+ newborn screening v0.233 LITAF Zornitza Stark Marked gene: LITAF as ready
BabyScreen+ newborn screening v0.233 LITAF Zornitza Stark Gene: litaf has been classified as Red List (Low Evidence).
BabyScreen+ newborn screening v0.233 LITAF Zornitza Stark Phenotypes for gene: LITAF were changed from Charcot-Marie-Tooth disease to Charcot-Marie-Tooth disease, type 1C, MIM# 601098
BabyScreen+ newborn screening v0.232 LITAF Zornitza Stark Mode of pathogenicity for gene: LITAF was changed from to None
BabyScreen+ newborn screening v0.231 LITAF Zornitza Stark Classified gene: LITAF as Red List (low evidence)
BabyScreen+ newborn screening v0.231 LITAF Zornitza Stark Gene: litaf has been classified as Red List (Low Evidence).
BabyScreen+ newborn screening v0.200 LITAF David Amor reviewed gene: LITAF: Rating: RED; Mode of pathogenicity: Loss-of-function variants (as defined in pop up message) DO NOT cause this phenotype - please provide details in the comments; Publications: ; Phenotypes: CMT1C; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
BabyScreen+ newborn screening v0.0 LITAF Zornitza Stark gene: LITAF was added
gene: LITAF was added to gNBS. Sources: BabySeq Category A gene,Expert Review Green
Mode of inheritance for gene: LITAF was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes for gene: LITAF were set to Charcot-Marie-Tooth disease