Identity
HGNC
LOCATION
19p13.12
LOCUSID
ALIAS
GPSN2,MRT14,SC2,TER
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: 9524
MIM: 610057
HGNC: 4551
Ensembl: ENSG00000099797
Variants:
dbSNP: 9524
ClinVar: 9524
TCGA: ENSG00000099797
COSMIC: TECR
RNA/Proteins
Expression (GTEx)
Pathways
Protein levels (Protein atlas)
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 38224948 | 2024 | Catalytic mechanism of trans-2-enoyl-CoA reductases in the fatty acid elongation cycle and its cooperative action with fatty acid elongases. | 0 |
| 38422897 | 2024 | The 3-hydroxyacyl-CoA dehydratase 1/2 form complex with trans-2-enoyl-CoA reductase involved in substrates transfer in very long chain fatty acid elongation. | 1 |
| 38224948 | 2024 | Catalytic mechanism of trans-2-enoyl-CoA reductases in the fatty acid elongation cycle and its cooperative action with fatty acid elongases. | 0 |
| 38422897 | 2024 | The 3-hydroxyacyl-CoA dehydratase 1/2 form complex with trans-2-enoyl-CoA reductase involved in substrates transfer in very long chain fatty acid elongation. | 1 |
| 25049234 | 2014 | Dual functions of the trans-2-enoyl-CoA reductase TER in the sphingosine 1-phosphate metabolic pathway and in fatty acid elongation. | 23 |
| 25049234 | 2014 | Dual functions of the trans-2-enoyl-CoA reductase TER in the sphingosine 1-phosphate metabolic pathway and in fatty acid elongation. | 23 |
| 24220030 | 2013 | Mutation for nonsyndromic mental retardation in the trans-2-enoyl-CoA reductase TER gene involved in fatty acid elongation impairs the enzyme activity and stability, leading to change in sphingolipid profile. | 14 |
| 24220030 | 2013 | Mutation for nonsyndromic mental retardation in the trans-2-enoyl-CoA reductase TER gene involved in fatty acid elongation impairs the enzyme activity and stability, leading to change in sphingolipid profile. | 14 |
| 21212097 | 2011 | Exome sequencing reveals a novel mutation for autosomal recessive non-syndromic mental retardation in the TECR gene on chromosome 19p13. | 41 |
| 21212097 | 2011 | Exome sequencing reveals a novel mutation for autosomal recessive non-syndromic mental retardation in the TECR gene on chromosome 19p13. | 41 |
| 15847654 | 2005 | A flexible array format for large-scale, rapid blood group DNA typing. | 35 |
| 15847654 | 2005 | A flexible array format for large-scale, rapid blood group DNA typing. | 35 |
Citation
Dessen P
TECR (trans-2,3-enoyl-CoA reductase)
Atlas Genet Cytogenet Oncol Haematol. 2014-07-01
Online version: http://atlasgeneticsoncology.org/gene/54061/tecr-(trans-2-3-enoyl-coa-reductase)
