Primary immunodeficiency or monogenic inflammatory bowel disease
Gene: ISG15
agree with green geneCreated: 17 Sep 2019, 3:18 p.m. | Last Modified: 17 Sep 2019, 3:18 p.m.
Panel Version: 1.94
YES- this is covered on our targeted exomeCreated: 17 Sep 2019, 3:18 p.m. | Last Modified: 17 Sep 2019, 3:18 p.m.
Panel Version: 1.94
Mode of inheritance
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
MSMD; idiopathic basal ganglia calcification
Gene rating submitted by Kimberly Gilmour and Austen Worth on behalf of London North GLH for the GMS Immunology specialist test group. As discussed with the GMS Immunology Specialist Test Group during webex call 28th March 2019 and confirmed in follow up email 6th September the Specialist Test Group all agreed there is enough evidence to rate this gene Green.Created: 17 Sep 2019, 3:18 p.m. | Last Modified: 17 Sep 2019, 3:18 p.m.
Panel Version: 1.94
Gene rating submitted by Tracy Briggs, David Gokhale and Abigal Rousseau on behalf of North West GLH for the GMS Immunology specialist test group. As discussed with the GMS Immunology Specialist Test Group during webex call 28th March 2019 and confirmed in follow up email on 20th June the Specialist Test Group all agreed there is enough evidence to rate this gene Green.Created: 17 Sep 2019, 3:18 p.m. | Last Modified: 17 Sep 2019, 3:18 p.m.
Panel Version: 1.94
OriginaI Metadata from IUIS classification table (February, 2018) downloaded 20180614. IUIS Genetic defect (original gene symbol in IUIS download): ISG15 .PanelApp HGNC gene symbol check: ISG15 . IUIS Disease: ISG15 deficiency . IUIS Inheritance: AR .T cells: Nl number, poor proliferation, .B cells: N/A, .IUIS Other affected cells: Ubiquitously expressed. IUIS Associated features: Susceptibility to mycobacteria, brain calcifications. IUIS Major category: Defects in Intrinsic and Innate Immunity. IUIS Subcategory: Mendelian Susceptibility to mycobacterial disease (MSMD)Created: 2 Jul 2018, 10:35 a.m.
Comment on list classification: Changed Amber to Green from external expert review and further publications to support gene-disease associationCreated: 21 Jun 2018, 10:43 p.m.
Comment on publications: Added publications suggested from external expert review to support upgrading of the gene to GreenCreated: 21 Jun 2018, 10:42 p.m.
Comment on phenotypes: Added phenotypes suggested from external expert reviewCreated: 21 Jun 2018, 10:26 p.m.
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(s) GOSH or GRID. In this combined PID panel, this gene has been rated as AMBER and needs further curational review to assess pertinence prior to v1.Created: 20 Apr 2018, 12:25 p.m.
Original metadata downloaded from ESID Registry. ESID_Gene_original: ISG15, PanelApp HGNC gene symbol check: ISG15, ESID classification: Main_category/ Sub_category/ PID_Diagnosis Phagocytic disorders / Defects with susceptibility to mycobacterial infection (MSMD) / Defects with susceptibility to mycobacterial infection (MSMD)Created: 17 Apr 2018, 12:29 p.m.
Original metadata supplied by GRID. GRID Gene Symbol HGNC PanelApp check: ISG15, GRID_Gene_Symbol: ISG15, GRID_Transcript_ENS_Community submitted: ENST00000379389, GRID_Transcript_RefSeq: NM_005101.3, GRID_Transcript_ENS_used_on_Production: ENST00000379389Created: 17 Apr 2018, 12:12 p.m.
Source NHS GMS was added to ISG15.
Source North West GLH was added to ISG15.
Source London North GLH was added to ISG15.
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.
Phenotypes for gene ISG15 were set to Immunodeficiency 38, 616126, Defects with susceptibility to mycobacterial infection (MSMD), idiopathic basal ganglia calcification, Susceptibility to mycobacteria, brain calcifications, Defects in Intrinsic and Innate Immunity
IUIS Classification February 2018 was added to ISG15. Panel: Primary immunodeficiency disorders
Victorian Clinical Genetics Services was added to ISG15. Panel: Primary immunodeficiency disorders
Gene: isg15 has been classified as Green List (High Evidence).
Gene: isg15 has been classified as Green List (High Evidence).
Publications for gene: ISG15 were set to 22859821; 25307056; 23579383
Publications for gene: ISG15 were set to 22859821; 25307056; 23579383; 25307056
Phenotypes for gene: ISG15 were set to Immunodeficiency 38, 616126; Defects with susceptibility to mycobacterial infection (MSMD); idiopathic basal ganglia calcification
Expert Review Amber was added to ISG15. Panel: Primary immunodeficiency disorders
ESID Registry 20171117 was added to ISG15. Panel: Primary immunodeficiency disorders Phenotypes for gene ISG15 were set to Immunodeficiency 38, Defects with susceptibility to mycobacterial infection (MSMD)
Phenotypes for gene ISG15 were set to Immunodeficiency 38
ISG15 was added to Primary immunodeficiency disorders panel. Sources: GRID V2.0
ISG15 was created by Louise Daugherty