Entity Details

Primary name TECRL
Entity type gene
Source Source Link

Details

PrimaryID253017
RefseqGeneNG_053152
SymbolTECRL
Nametrans-2,3-enoyl-CoA reductase like
Chromosome4
Location4q13.1
TaxID9606
Statuslive
SourceGenomegenomic
SourceOriginnatural
CreationDate2002-07-27
ModificationDate2021-06-11

Ontological Relatives

UniProt IDsTECRL_HUMAN

GO terms

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GOName
GO:0005783 endoplasmic reticulum
GO:0016021 integral component of membrane
GO:0016491 oxidoreductase activity
GO:0016627 oxidoreductase activity, acting on the CH-CH group of donors
GO:0042761 very long-chain fatty acid biosynthetic process

Diseases

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Disease IDSourceNameDescription
614021 OMIMVentricular tachycardia, catecholaminergic polymorphic, 3 (CPVT3)An arrhythmogenic disorder characterized by stress-induced, bidirectional ventricular tachycardia that may degenerate into cardiac arrest and cause sudden death. Patients present with recurrent syncope, or sudden death after physical activity or emotional stress. CPVT3 is an autosomal recessive disorder with onset at early age and associated with sudden death in childhood. Patients manifest QT prolongation on adrenergic stimulation. The disease is caused by variants affecting the gene represented in this entry.

Interactions

1 interaction

InteractorPartnerSourcesPublicationsLink
TECRLFBXO7BioGRID27503909 details