Cardiac arrhythmias - previous panel
Gene: TRPM4EnsemblGeneIds (GRCh38): ENSG00000130529
EnsemblGeneIds (GRCh37): ENSG00000130529
OMIM: 606936, Gene2Phenotype
TRPM4 is in 4 panels
1 review
Eleanor Williams (Genomics England Curator)
Comment on phenotypes: Added phenotype from OMIM that was missing from source panel Brugada syndromeCreated: 16 Jan 2019, 11:57 a.m.
Details
- Mode of Inheritance
- MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
- Sources
-
- Expert Review Green
- Phenotypes
-
- Progressive familial heart block, type IB 604559
- OMIM
- 606936
- Clinvar variants
- Variants in TRPM4
- Penetrance
- None
- Publications
-
- http://www.ncbi.nlm.nih.gov/pubmed/23382873
- Panels with this gene
History Filter Activity
Panel promoted to version 1.0
Ellen McDonagh (Genomics England Curator)Eleanor Williams: Comment on phenotypes: Added p
Set Phenotypes
Eleanor Williams (Genomics England Curator)Phenotypes for gene: TRPM4 were changed from to Progressive familial heart block, type IB 604559
Created, Added New Source, Set mode of inheritance, Set publications
Rebecca Foulger (Genomics England curator)gene: TRPM4 was added gene: TRPM4 was added to Cardiac arrythmias. Sources: Expert Review Green Mode of inheritance for gene: TRPM4 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown Publications for gene: TRPM4 were set to http://www.ncbi.nlm.nih.gov/pubmed/23382873