Activity

Filter

Cancel
Date Panel Item Activity
10 actions
BabyScreen+ newborn screening v1.114 RNASEH2C Tommy Li Added phenotypes Aicardi-Goutieres syndrome 3, MIM# 610329 for gene: RNASEH2C
BabyScreen+ newborn screening v0.1440 RNASEH2C Zornitza Stark Marked gene: RNASEH2C as ready
BabyScreen+ newborn screening v0.1440 RNASEH2C Zornitza Stark Gene: rnaseh2c has been classified as Amber List (Moderate Evidence).
BabyScreen+ newborn screening v0.1440 RNASEH2C Zornitza Stark Phenotypes for gene: RNASEH2C were changed from Aicardi-Goutieres syndrome to Aicardi-Goutieres syndrome 3, MIM# 610329
BabyScreen+ newborn screening v0.1439 RNASEH2C Zornitza Stark Publications for gene: RNASEH2C were set to
BabyScreen+ newborn screening v0.1438 RNASEH2C Zornitza Stark Classified gene: RNASEH2C as Amber List (moderate evidence)
BabyScreen+ newborn screening v0.1438 RNASEH2C Zornitza Stark Gene: rnaseh2c has been classified as Amber List (Moderate Evidence).
BabyScreen+ newborn screening v0.1437 RNASEH2C Zornitza Stark Tag for review tag was added to gene: RNASEH2C.
Tag neurological tag was added to gene: RNASEH2C.
BabyScreen+ newborn screening v0.1437 RNASEH2C Zornitza Stark reviewed gene: RNASEH2C: Rating: AMBER; Mode of pathogenicity: None; Publications: 32877590; Phenotypes: Aicardi-Goutieres syndrome 3, MIM# 610329; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
BabyScreen+ newborn screening v0.0 RNASEH2C Zornitza Stark gene: RNASEH2C was added
gene: RNASEH2C was added to gNBS. Sources: BabySeq Category A gene,Expert Review Green
Mode of inheritance for gene: RNASEH2C was set to BIALLELIC, autosomal or pseudoautosomal
Phenotypes for gene: RNASEH2C were set to Aicardi-Goutieres syndrome