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Genomic newborn screening: BabyScreen+ v0.359 ZEB2 Zornitza Stark Marked gene: ZEB2 as ready
Genomic newborn screening: BabyScreen+ v0.359 ZEB2 Zornitza Stark Gene: zeb2 has been classified as Red List (Low Evidence).
Genomic newborn screening: BabyScreen+ v0.359 ZEB2 Zornitza Stark Phenotypes for gene: ZEB2 were changed from Mowat-Wilson syndrome to Mowat-Wilson syndrome MIM# 235730
Genomic newborn screening: BabyScreen+ v0.358 ZEB2 Zornitza Stark Publications for gene: ZEB2 were set to
Genomic newborn screening: BabyScreen+ v0.357 ZEB2 Zornitza Stark Classified gene: ZEB2 as Red List (low evidence)
Genomic newborn screening: BabyScreen+ v0.357 ZEB2 Zornitza Stark Gene: zeb2 has been classified as Red List (Low Evidence).
Genomic newborn screening: BabyScreen+ v0.274 ZEB2 Lilian Downie reviewed gene: ZEB2: Rating: RED; Mode of pathogenicity: None; Publications: PMID: 20301585; Phenotypes: Mowat-Wilson syndrome MIM# 235730; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Genomic newborn screening: BabyScreen+ v0.0 ZEB2 Zornitza Stark gene: ZEB2 was added
gene: ZEB2 was added to gNBS. Sources: BabySeq Category A gene,Expert Review Green
Mode of inheritance for gene: ZEB2 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes for gene: ZEB2 were set to Mowat-Wilson syndrome