Identity
HGNC
LOCATION
4q13.1
LOCUSID
ALIAS
CPVT3,GPSN2L,SRD5A2L2,TERL
FUSION GENES
Non-annotated gene. Preliminary data : if you are an author who wish to write a full paper/card on this gene, contribute in submission tool
Other Information
Locus ID:
NCBI: 253017
MIM: 617242
HGNC: 27365
Ensembl: ENSG00000205678
Variants:
dbSNP: 253017
ClinVar: 253017
TCGA: ENSG00000205678
COSMIC: TECRL
RNA/Proteins
| Gene ID | Transcript ID | Uniprot |
|---|---|---|
| ENSG00000205678 | ENST00000381210 | Q5HYJ1 |
| ENSG00000205678 | ENST00000507440 | E9PD39 |
| ENSG00000205678 | ENST00000509536 | D6RBZ3 |
| ENSG00000205678 | ENST00000511997 | H0Y9F0 |
Expression (GTEx)
Pathways
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 35577932 | 2022 | TECRL deficiency results in aberrant mitochondrial function in cardiomyocytes. | 5 |
| 35577932 | 2022 | TECRL deficiency results in aberrant mitochondrial function in cardiomyocytes. | 5 |
| 32173957 | 2020 | Novel variants in TECRL cause recessive inherited CPVT type 3 with severe and variable clinical symptoms. | 13 |
| 32173957 | 2020 | Novel variants in TECRL cause recessive inherited CPVT type 3 with severe and variable clinical symptoms. | 13 |
| 30790670 | 2019 | A compound heterozygosity of Tecrl gene confirmed in a catecholaminergic polymorphic ventricular tachycardia family. | 14 |
| 30790670 | 2019 | A compound heterozygosity of Tecrl gene confirmed in a catecholaminergic polymorphic ventricular tachycardia family. | 14 |
| 27861123 | 2016 | TECRL, a new life-threatening inherited arrhythmia gene associated with overlapping clinical features of both LQTS and CPVT. | 57 |
| 27861123 | 2016 | TECRL, a new life-threatening inherited arrhythmia gene associated with overlapping clinical features of both LQTS and CPVT. | 57 |
| 20379614 | 2010 | Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score. | 78 |
| 20628086 | 2010 | Variation at the NFATC2 locus increases the risk of thiazolidinedione-induced edema in the Diabetes REduction Assessment with ramipril and rosiglitazone Medication (DREAM) study. | 15 |
| 20379614 | 2010 | Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score. | 78 |
| 20628086 | 2010 | Variation at the NFATC2 locus increases the risk of thiazolidinedione-induced edema in the Diabetes REduction Assessment with ramipril and rosiglitazone Medication (DREAM) study. | 15 |
| 19913121 | 2009 | Gene-centric association signals for lipids and apolipoproteins identified via the HumanCVD BeadChip. | 105 |
| 19913121 | 2009 | Gene-centric association signals for lipids and apolipoproteins identified via the HumanCVD BeadChip. | 105 |
Citation
Dessen P
TECRL (trans-2,3-enoyl-CoA reductase like)
Atlas Genet Cytogenet Oncol Haematol. 2014-11-01
Online version: http://atlasgeneticsoncology.org/gene/74611/tecrl-(trans-2-3-enoyl-coa-reductase-like)
