Activity

Filter

Cancel
Date Panel Item Activity
14 actions
Renal Ciliopathies and Nephronophthisis v1.40 B9D1 Zornitza Stark Phenotypes for gene: B9D1 were changed from Meckel syndrome 9, OMIM #614209; Joubert syndrome 27, OMIM #617120 to Ciliopathy, MONDO:0005308, B9D1-related
Renal Ciliopathies and Nephronophthisis v1.39 B9D1 Zornitza Stark Publications for gene: B9D1 were set to
Renal Ciliopathies and Nephronophthisis v1.38 B9D1 Zornitza Stark Classified gene: B9D1 as Green List (high evidence)
Renal Ciliopathies and Nephronophthisis v1.38 B9D1 Zornitza Stark Gene: b9d1 has been classified as Green List (High Evidence).
Renal Ciliopathies and Nephronophthisis v1.37 B9D1 Zornitza Stark edited their review of gene: B9D1: Added comment: Lumped by ClinGen. Additional families reported, upgrade to Green.; Changed rating: GREEN; Changed publications: 24886560, 21493627, 25920555, 40565534, 40933483; Changed phenotypes: Ciliopathy, MONDO:0005308, B9D1-related
Renal Ciliopathies and Nephronophthisis v0.90 B9D1 Zornitza Stark Marked gene: B9D1 as ready
Renal Ciliopathies and Nephronophthisis v0.90 B9D1 Zornitza Stark Gene: b9d1 has been classified as Red List (Low Evidence).
Renal Ciliopathies and Nephronophthisis v0.90 B9D1 Zornitza Stark Phenotypes for gene: B9D1 were changed from Meckel syndrome 9, OMIM #614209; Joubert syndrome 27, OMIM #617120 to Meckel syndrome 9, OMIM #614209; Joubert syndrome 27, OMIM #617120
Renal Ciliopathies and Nephronophthisis v0.89 B9D1 Zornitza Stark Phenotypes for gene: B9D1 were changed from to Meckel syndrome 9, OMIM #614209; Joubert syndrome 27, OMIM #617120
Renal Ciliopathies and Nephronophthisis v0.89 B9D1 Zornitza Stark Mode of inheritance for gene: B9D1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Renal Ciliopathies and Nephronophthisis v0.32 B9D1 Chirag Patel Classified gene: B9D1 as Red List (low evidence)
Renal Ciliopathies and Nephronophthisis v0.32 B9D1 Chirag Patel Gene: b9d1 has been classified as Red List (Low Evidence).
Renal Ciliopathies and Nephronophthisis v0.31 B9D1 Chirag Patel reviewed gene: B9D1: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ?Meckel syndrome 9, OMIM #614209, Joubert syndrome 27, OMIM #617120; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Renal Ciliopathies and Nephronophthisis v0.0 B9D1 Zornitza Stark gene: B9D1 was added
gene: B9D1 was added to Renal ciliopathies and nephronophthisis_KidGen. Sources: Expert Review Green,KidGen_CilioNephronop v38.1.0
Mode of inheritance for gene: B9D1 was set to Unknown