Dilated Cardiomyopathy (DCM)
Gene: TMPOEnsemblGeneIds (GRCh38): ENSG00000120802
EnsemblGeneIds (GRCh37): ENSG00000120802
OMIM: 188380, Gene2Phenotype
TMPO is in 3 panels
2 reviews
Rebecca Foulger (Genomics England curator)
Comment on list classification: Changed rating from Amber to Red based on new evidence in OMIM: The variant R690C, formerly designated CARDIOMYOPATHY, DILATED, 1T, has been reclassified as a VARIANT OF UNKNOWN SIGNIFICANCE.Created: 11 May 2017, 9:40 a.m.
Oxford Medical Genetics Laboratory (OUH NHS Foundation Trust)
Details
- Mode of Inheritance
- MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
- Sources
-
- Expert Review Red
- UKGTN
- Expert list
- Illumina TruGenome Clinical Sequencing Services
- Phenotypes
-
- Dilated Cardiomyopathy, Dominant
- OMIM
- 188380
- Clinvar variants
- Variants in TMPO
- Penetrance
- Complete
- Panels with this gene
History Filter Activity
Gene classified by Genomics England curator
Rebecca Foulger (Genomics England curator)This gene has been classified as Red List (Low Evidence).
Added New Source
Ellen McDonagh (Genomics England Curator)TMPO was added to Dilated Cardiomyopathy (DCM)panel. Sources: UKGTN
Set Mode of Inheritance
Ellen McDonagh (Genomics England Curator)Model of inheritance for gene TMPO was changed to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Added New Source
Ellen McDonagh (Genomics England Curator)TMPO was added to Dilated Cardiomyopathy (DCM)panel. Sources: Illumina TruGenome Clinical Sequencing Services,Expert list
Added New Source
Ellen McDonagh (Genomics England Curator)TMPO was added to Dilated Cardiomyopathy (DCM)panel. Sources: Illumina TruGenome Clinical Sequencing Services,Expert list