Brugada syndrome and cardiac sodium channel disease
Gene: DLG1EnsemblGeneIds (GRCh38): ENSG00000075711
EnsemblGeneIds (GRCh37): ENSG00000075711
OMIM: 601014, Gene2Phenotype
DLG1 is in 4 panels
3 reviews
Rebecca Whittington (South West GLH)
No links to phenotypes on OMIMCreated: 25 Mar 2019, 4:30 p.m.
No strong evidence for this geneCreated: 25 Mar 2019, 4:27 p.m.
Mode of inheritance
Unknown
Caroline Wright (Genomics England Curator)
Comment when marking as ready: Not on Manchester diagnostic panelCreated: 11 Feb 2016, 12:22 p.m.
Oxford Medical Genetics Laboratory (OUH NHS Foundation Trust)
Details
- Mode of Inheritance
- Unknown
- Sources
-
- Expert Review Red
- South West GLH
- Phenotypes
-
- Brugada syndrome, MONDO:0015263
- OMIM
- 601014
- Clinvar variants
- Variants in DLG1
- Penetrance
- Complete
- Panels with this gene
History Filter Activity
Set Phenotypes
Ivone Leong (Genomics England Curator)Phenotypes for gene: DLG1 were changed from to Brugada syndrome, MONDO:0015263
Entity classified by Genomics England curator
Ellen McDonagh (Genomics England Curator)Gene: dlg1 has been classified as Red List (Low Evidence).
Added New Source, Set mode of inheritance, Status Update
Ellen McDonagh (Genomics England Curator)Source South West GLH was added to DLG1. Mode of inheritance for gene DLG1 was changed from to Unknown Rating Changed from Red List (low evidence) to No List (delete)
Approved Gene
Caroline Wright (Genomics England Curator)This proposed gene was validated and added to this panel
Gene classified by Genomics England curator
Caroline Wright (Genomics England Curator)This gene has been removed from the panel.
Added New Source
Oxford Medical Genetics Laboratory (OUH NHS Foundation Trust)DLG1 was added to Brugada syndromepanel. Sources: Oxford Medical Genetics Laboratory
Created
Oxford Medical Genetics Laboratory (OUH NHS Foundation Trust)DLG1 was created by OxfordGenetics