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Bleeding and Platelet Disorders v0.272 GP9 Zornitza Stark Marked gene: GP9 as ready
Bleeding and Platelet Disorders v0.272 GP9 Zornitza Stark Gene: gp9 has been classified as Green List (High Evidence).
Bleeding and Platelet Disorders v0.272 GP9 Zornitza Stark Phenotypes for gene: GP9 were changed from to Bernard-Soulier syndrome, type C, MIM# 231200
Bleeding and Platelet Disorders v0.271 GP9 Zornitza Stark Publications for gene: GP9 were set to
Bleeding and Platelet Disorders v0.270 GP9 Zornitza Stark Mode of inheritance for gene: GP9 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Bleeding and Platelet Disorders v0.269 GP9 Zornitza Stark edited their review of gene: GP9: Added comment: Bernard-Soulier syndrome is a bleeding disorder caused by a defect in or deficiency of the platelet membrane von Willebrand factor receptor complex, glycoprotein Ib (GP Ib). GP Ib is composed of 4 subunits encoded by 4 separate genes: GP1BA, GP1BB, GP9, and GP5.

At least 3 unrelated families reported, animal model.; Changed publications: 8049428, 33553065, 32030720, 31484196
Bleeding and Platelet Disorders v0.269 GP9 Zornitza Stark reviewed gene: GP9: Rating: GREEN; Mode of pathogenicity: None; Publications: 8049428; Phenotypes: Bernard-Soulier syndrome, type C, MIM# 231200; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Bleeding and Platelet Disorders v0.0 GP9 Zornitza Stark gene: GP9 was added
gene: GP9 was added to Bleeding Disorders_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services
Mode of inheritance for gene: GP9 was set to Unknown