Activity

Filter

Cancel
Date Panel Item Activity
7 actions
Skeletal ciliopathies v3.23 CENPF Arina Puzriakova Phenotypes for gene: CENPF were changed from Stromme syndrome, 243605; Lethal fetal brain malformation-duodenal atresia-bilateral renal hypoplasia syndrome to Stromme syndrome, OMIM:243605; Lethal fetal brain malformation-duodenal atresia-bilateral renal hypoplasia syndrome
Skeletal ciliopathies v1.10 CENPF Arina Puzriakova Tag curated_removed tag was added to gene: CENPF.
Skeletal ciliopathies v0.16 CENPF Eleanor Williams Classified gene: CENPF as No list
Skeletal ciliopathies v0.16 CENPF Eleanor Williams Added comment: Comment on list classification: After consultation with the Genomics England clinical team, removing this gene from the skeletal ciliopathies panel as the phenotype is polydactyly only.
Skeletal ciliopathies v0.16 CENPF Eleanor Williams Gene: cenpf has been removed from the panel.
Skeletal ciliopathies v0.15 CENPF Eleanor Williams commented on gene: CENPF
Skeletal ciliopathies v0.1 CENPF Eleanor Williams gene: CENPF was added
gene: CENPF was added to Skeletal ciliopathies. Sources: Radboud University Medical Center, Nijmegen,Orphanet,Expert Review Green
Mode of inheritance for gene: CENPF was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: CENPF were set to 26820108
Phenotypes for gene: CENPF were set to Stromme syndrome, 243605; Lethal fetal brain malformation-duodenal atresia-bilateral renal hypoplasia syndrome