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Congenital Disorders of Glycosylation v0.84 PAPSS2 Zornitza Stark Marked gene: PAPSS2 as ready
Congenital Disorders of Glycosylation v0.84 PAPSS2 Zornitza Stark Gene: papss2 has been classified as Red List (Low Evidence).
Congenital Disorders of Glycosylation v0.83 PAPSS2 Zornitza Stark Phenotypes for gene: PAPSS2 were changed from to Brachyolmia 4 with mild epiphyseal and metaphyseal changes MIM#612847
Congenital Disorders of Glycosylation v0.82 PAPSS2 Zornitza Stark Publications for gene: PAPSS2 were set to
Congenital Disorders of Glycosylation v0.81 PAPSS2 Zornitza Stark Mode of inheritance for gene: PAPSS2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Congenital Disorders of Glycosylation v0.80 PAPSS2 Zornitza Stark Classified gene: PAPSS2 as Red List (low evidence)
Congenital Disorders of Glycosylation v0.80 PAPSS2 Zornitza Stark Gene: papss2 has been classified as Red List (Low Evidence).
Congenital Disorders of Glycosylation v0.57 PAPSS2 Naomi Baker reviewed gene: PAPSS2: Rating: RED; Mode of pathogenicity: None; Publications: PMID: 22791835, 25594860, 31461705, 23633440, 9771708, 19474428.; Phenotypes: Brachyolmia 4 with mild epiphyseal and metaphyseal changes MIM#612847; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Congenital Disorders of Glycosylation v0.0 PAPSS2 Zornitza Stark gene: PAPSS2 was added
gene: PAPSS2 was added to Congenital Disorders of Glycosylation_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services
Mode of inheritance for gene: PAPSS2 was set to Unknown