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Genomic newborn screening: BabyScreen+ v0.515 WFS1 Zornitza Stark Marked gene: WFS1 as ready
Genomic newborn screening: BabyScreen+ v0.515 WFS1 Zornitza Stark Gene: wfs1 has been classified as Red List (Low Evidence).
Genomic newborn screening: BabyScreen+ v0.515 WFS1 Zornitza Stark Phenotypes for gene: WFS1 were changed from Wolfram syndrome to Wolfram syndrome MIM#222300
Genomic newborn screening: BabyScreen+ v0.514 WFS1 Zornitza Stark Publications for gene: WFS1 were set to
Genomic newborn screening: BabyScreen+ v0.513 WFS1 Zornitza Stark Classified gene: WFS1 as Red List (low evidence)
Genomic newborn screening: BabyScreen+ v0.513 WFS1 Zornitza Stark Gene: wfs1 has been classified as Red List (Low Evidence).
Genomic newborn screening: BabyScreen+ v0.503 WFS1 Lilian Downie reviewed gene: WFS1: Rating: RED; Mode of pathogenicity: None; Publications: PMID: 20301750, PMID: 11317350, PMID: 20738327, PMID: 31337416; Phenotypes: Wolfram syndrome MIM#222300; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Genomic newborn screening: BabyScreen+ v0.0 WFS1 Zornitza Stark gene: WFS1 was added
gene: WFS1 was added to gNBS. Sources: BabySeq Category A gene,Expert Review Green
Mode of inheritance for gene: WFS1 was set to BIALLELIC, autosomal or pseudoautosomal
Phenotypes for gene: WFS1 were set to Wolfram syndrome