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Genomic newborn screening: BabyScreen+ v0.91 ANKH Zornitza Stark Marked gene: ANKH as ready
Genomic newborn screening: BabyScreen+ v0.91 ANKH Zornitza Stark Gene: ankh has been classified as Red List (Low Evidence).
Genomic newborn screening: BabyScreen+ v0.91 ANKH Zornitza Stark Phenotypes for gene: ANKH were changed from Craniometaphyseal dysplasia to Craniometaphyseal dysplasia MIM#123000
Genomic newborn screening: BabyScreen+ v0.90 ANKH Zornitza Stark Classified gene: ANKH as Red List (low evidence)
Genomic newborn screening: BabyScreen+ v0.90 ANKH Zornitza Stark Gene: ankh has been classified as Red List (Low Evidence).
Genomic newborn screening: BabyScreen+ v0.89 ANKH Zornitza Stark reviewed gene: ANKH: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Craniometaphyseal dysplasia MIM#123000; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Genomic newborn screening: BabyScreen+ v0.0 ANKH Zornitza Stark gene: ANKH was added
gene: ANKH was added to gNBS. Sources: BabySeq Category A gene,Expert Review Green
Mode of inheritance for gene: ANKH was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes for gene: ANKH were set to Craniometaphyseal dysplasia