Long QT syndrome

Gene: TECRL

Red List (low evidence)

TECRL (trans-2,3-enoyl-CoA reductase like)
EnsemblGeneIds (GRCh38): ENSG00000205678
EnsemblGeneIds (GRCh37): ENSG00000205678
OMIM: 617242, Gene2Phenotype
TECRL is in 2 panels

1 review

Ivone Leong (Genomics England Curator)

I don't know

New gene submitted on behalf of the GMS Cardiology specialist group. The group has agreed that this gene should be Amber on this panel.
Sources: NHS GMS
Created: 18 Nov 2019, 2:07 p.m.

Mode of inheritance
BIALLELIC, autosomal or pseudoautosomal

Phenotypes
Ventricular tachycardia, catecholaminergic polymorphic, 3, 614021

Details

Mode of Inheritance
BIALLELIC, autosomal or pseudoautosomal
Sources
  • NHS GMS
Phenotypes
  • Ventricular tachycardia, catecholaminergic polymorphic, 3, 614021
OMIM
617242
Clinvar variants
Variants in TECRL
Penetrance
None
Panels with this gene

History Filter Activity

18 Nov 2019, Gel status: 1

Created, Added New Source, Set mode of inheritance, Set Phenotypes

Ivone Leong (Genomics England Curator)

gene: TECRL was added gene: TECRL was added to Long QT syndrome. Sources: NHS GMS Mode of inheritance for gene: TECRL was set to BIALLELIC, autosomal or pseudoautosomal Phenotypes for gene: TECRL were set to Ventricular tachycardia, catecholaminergic polymorphic, 3, 614021 Review for gene: TECRL was set to AMBER