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Craniosynostosis v0.147 ZEB2 Bryony Thompson Marked gene: ZEB2 as ready
Craniosynostosis v0.147 ZEB2 Bryony Thompson Gene: zeb2 has been classified as Amber List (Moderate Evidence).
Craniosynostosis v0.147 ZEB2 Bryony Thompson Classified gene: ZEB2 as Amber List (moderate evidence)
Craniosynostosis v0.147 ZEB2 Bryony Thompson Gene: zeb2 has been classified as Amber List (Moderate Evidence).
Craniosynostosis v0.146 ZEB2 Bryony Thompson Mode of inheritance for gene: ZEB2 was changed from BIALLELIC, autosomal or pseudoautosomal to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Craniosynostosis v0.145 ZEB2 Bryony Thompson edited their review of gene: ZEB2: Changed mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Craniosynostosis v0.145 ZEB2 Bryony Thompson gene: ZEB2 was added
gene: ZEB2 was added to Craniosynostosis. Sources: Literature
Mode of inheritance for gene: ZEB2 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: ZEB2 were set to 25123255; 18076118
Phenotypes for gene: ZEB2 were set to Mowat-Wilson syndrome MIM#235730
Review for gene: ZEB2 was set to AMBER
Added comment: Identified 3 unrelated cases with cranionsynostosis as a prominent feature of the condition. However, the last report was in 2014.
Sources: Literature