Primary immunodeficiency or monogenic inflammatory bowel disease
Gene: FBF1
Comment on list classification: Changed from Amber to Red, no published cases of immunodeficiency to date. Red review from external expert review. Referred back to Victorian Clinical Genetics Services for evidences.Created: 3 Jul 2018, 12:24 p.m.
Comment on list classification: This gene was absent from the original PanelApp PID panel dataset (review April 2018). However it was listed in external expert immunodeficiency diagnostic gene list from Victorian Clinical Genetics Services. In this combined PID panel, this gene has been rated as AMBER and needs further curational review to assess pertinence prior to v1. No disorder or MOI was listed in the submitted list.Created: 26 Jun 2018, 12:46 p.m.
2018-07-12 Louise Daugherty (Genomics England Curator) promoted panel to v1.0. Reviews were assessed, and panel was revised according to expert reviews and further in-house curation based on PanelApp guidelines. Previous panels (A- or hypo-gammaglobulinaemia, Congenital neutropaenia, Agranulocytosis, Combined B and T cell defect, Inherited complement deficiency and SCID panels) that were merged with this panel, were checked again for any changes/new reviews prior to versioning of this panel, these merged panels are now retired/made internal.
Gene: fbf1 has been classified as Red List (Low Evidence).
Gene: fbf1 has been classified as Red List (Low Evidence).
Gene: fbf1 has been classified as Amber List (Moderate Evidence).
FBF1 was added to Primary immunodeficiency disorders panel. Sources: Victorian Clinical Genetics Services
FBF1 was created by Louise Daugherty