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BabyScreen+ newborn screening v0.382 MSX2 Zornitza Stark Marked gene: MSX2 as ready
BabyScreen+ newborn screening v0.382 MSX2 Zornitza Stark Gene: msx2 has been classified as Red List (Low Evidence).
BabyScreen+ newborn screening v0.382 MSX2 Zornitza Stark Phenotypes for gene: MSX2 were changed from Parietal foramina 1 to Craniosynostosis 2 (MIM#604757); Parietal foramina 1 (MIM#168500); Parietal foramina with cleidocranial dysplasia (MIM#168550)
BabyScreen+ newborn screening v0.381 MSX2 Zornitza Stark Classified gene: MSX2 as Red List (low evidence)
BabyScreen+ newborn screening v0.381 MSX2 Zornitza Stark Gene: msx2 has been classified as Red List (Low Evidence).
BabyScreen+ newborn screening v0.380 MSX2 Zornitza Stark reviewed gene: MSX2: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Craniosynostosis 2 (MIM#604757), Parietal foramina 1 (MIM#168500), Parietal foramina with cleidocranial dysplasia (MIM#168550); Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
BabyScreen+ newborn screening v0.274 MSX2 David Amor reviewed gene: MSX2: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Craniosynostosis, parietal foramina; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
BabyScreen+ newborn screening v0.0 MSX2 Zornitza Stark gene: MSX2 was added
gene: MSX2 was added to gNBS. Sources: BabySeq Category A gene,Expert Review Green
Mode of inheritance for gene: MSX2 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes for gene: MSX2 were set to Parietal foramina 1