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Red cell disorders v2.0 BPGM Gene migrated from ENSG00000172331 to ENSG00000172331 (gene set migration)
Red cell disorders v1.52 BPGM Bryony Thompson Publications for gene: BPGM were set to 1421379; 27651169; 25015942
Red cell disorders v1.51 BPGM Bryony Thompson Mode of inheritance for gene: BPGM was changed from BOTH monoallelic and biallelic, autosomal or pseudoautosomal to BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal
Red cell disorders v1.50 BPGM Bryony Thompson Classified gene: BPGM as Green List (high evidence)
Red cell disorders v1.50 BPGM Bryony Thompson Gene: bpgm has been classified as Green List (High Evidence).
Red cell disorders v1.49 Bryony Thompson Added reviews for gene BPGM from panel Mendeliome
Red cell disorders v0.145 BPGM Zornitza Stark Marked gene: BPGM as ready
Red cell disorders v0.145 BPGM Zornitza Stark Gene: bpgm has been classified as Amber List (Moderate Evidence).
Red cell disorders v0.145 BPGM Zornitza Stark Classified gene: BPGM as Amber List (moderate evidence)
Red cell disorders v0.145 BPGM Zornitza Stark Gene: bpgm has been classified as Amber List (Moderate Evidence).
Red cell disorders v0.144 BPGM Zornitza Stark gene: BPGM was added
gene: BPGM was added to Red cell disorders. Sources: Expert list
Mode of inheritance for gene: BPGM was set to BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Publications for gene: BPGM were set to 1421379; 27651169; 25015942
Phenotypes for gene: BPGM were set to Erythrocytosis, familial, 8, MIM# 222800
Review for gene: BPGM was set to AMBER
Added comment: Mixture of mono-allelic and bi-allelic variants reported, MOI uncertain.
Sources: Expert list