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Bleeding and Platelet Disorders v0.208 MPI Zornitza Stark Marked gene: MPI as ready
Bleeding and Platelet Disorders v0.208 MPI Zornitza Stark Gene: mpi has been classified as Green List (High Evidence).
Bleeding and Platelet Disorders v0.208 MPI Zornitza Stark Classified gene: MPI as Green List (high evidence)
Bleeding and Platelet Disorders v0.208 MPI Zornitza Stark Gene: mpi has been classified as Green List (High Evidence).
Bleeding and Platelet Disorders v0.207 MPI Zornitza Stark gene: MPI was added
gene: MPI was added to Bleeding and Platelet Disorders. Sources: Expert Review
Mode of inheritance for gene: MPI was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: MPI were set to 12414827; 9585601; 10980531; 33098580; 33204592; 32905087; 32266963; 30242110
Phenotypes for gene: MPI were set to Congenital disorder of glycosylation, type Ib, MIM# 602579; MPI-CDG MONDO:0011257
Review for gene: MPI was set to GREEN
Added comment: CDG Ib is clinically distinct from most other CDGs by the lack of significant central nervous system involvement. The predominant symptoms are chronic diarrhoea with failure to thrive and protein-losing enteropathy with coagulopathy. Both bleeding and thrombosis reported. Some individuals develop hepatic fibrosis. CDG Ib is also different from other CDGs in that it can be treated effectively with oral mannose supplementation, but can be fatal if untreated.

Well established gene-disease association, numerous families reported.
Sources: Expert Review
Bleeding and Platelet Disorders v0.118 MPIG6B Zornitza Stark Marked gene: MPIG6B as ready
Bleeding and Platelet Disorders v0.118 MPIG6B Zornitza Stark Gene: mpig6b has been classified as Green List (High Evidence).
Bleeding and Platelet Disorders v0.118 MPIG6B Zornitza Stark Classified gene: MPIG6B as Green List (high evidence)
Bleeding and Platelet Disorders v0.118 MPIG6B Zornitza Stark Gene: mpig6b has been classified as Green List (High Evidence).
Bleeding and Platelet Disorders v0.117 MPIG6B Zornitza Stark gene: MPIG6B was added
gene: MPIG6B was added to Bleeding Disorders. Sources: Expert list
Mode of inheritance for gene: MPIG6B was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: MPIG6B were set to 31276734; 29898956; 27743390
Phenotypes for gene: MPIG6B were set to Thrombocytopenia, anemia, and myelofibrosis, MIM# 617441
Review for gene: MPIG6B was set to GREEN
Added comment: Six families reported.
Sources: Expert list