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Genomic newborn screening: BabyScreen+ v0.187 ACVR1 Zornitza Stark Marked gene: ACVR1 as ready
Genomic newborn screening: BabyScreen+ v0.187 ACVR1 Zornitza Stark Gene: acvr1 has been classified as Red List (Low Evidence).
Genomic newborn screening: BabyScreen+ v0.187 ACVR1 Zornitza Stark Phenotypes for gene: ACVR1 were changed from Fibrodysplasia ossificans progressiva to Fibrodysplasia ossificans progressiva, MIM# 135100
Genomic newborn screening: BabyScreen+ v0.186 ACVR1 Zornitza Stark Publications for gene: ACVR1 were set to
Genomic newborn screening: BabyScreen+ v0.185 ACVR1 Zornitza Stark Classified gene: ACVR1 as Red List (low evidence)
Genomic newborn screening: BabyScreen+ v0.185 ACVR1 Zornitza Stark Gene: acvr1 has been classified as Red List (Low Evidence).
Genomic newborn screening: BabyScreen+ v0.184 ACVR1 Zornitza Stark Tag for review tag was added to gene: ACVR1.
Tag clinical trial tag was added to gene: ACVR1.
Genomic newborn screening: BabyScreen+ v0.184 ACVR1 Zornitza Stark reviewed gene: ACVR1: Rating: RED; Mode of pathogenicity: None; Publications: 16642017, 29089047, 35384641; Phenotypes: Fibrodysplasia ossificans progressiva, MIM# 135100; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Genomic newborn screening: BabyScreen+ v0.0 ACVR1 Zornitza Stark gene: ACVR1 was added
gene: ACVR1 was added to gNBS. Sources: BabySeq Category A gene,Expert Review Green
Mode of inheritance for gene: ACVR1 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes for gene: ACVR1 were set to Fibrodysplasia ossificans progressiva