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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
trans-2,3-enoyl-CoA reductase
Summary
- Gene Symbol
-
- TECR
- Aliases
-
- MRT14
- TER
- very-long-chain enoyl-CoA reductase
- Organism
- Homo sapiens (human)
Annotation
- Keyword
-
- 3D-structure
- Acetylation
- Alternative splicing
- Disease variant
- Endoplasmic reticulum
- Fatty acid biosynthesis
- Glycoprotein
- Intellectual disability
- NADP
- Oxidoreductase
- Phosphoprotein
- Reference proteome
- Sphingolipid metabolism
- Transmembrane helix
- Proteins
Gene Ontology (GO)
| GO Term | Evidence Code | PMID |
|---|---|---|
| fatty acid elongation | ||
| sphingolipid metabolic process | ||
| very long-chain fatty acid biosynthetic process | ||
| long-chain fatty-acyl-CoA biosynthetic process |
|
GO Hierarchy
biological process
metabolic process [inference]
nitrogen compound metabolic process [inference]
cellular nitrogen compound metabolic process [inference]
nucleobase-containing compound metabolic process [inference]
cellular nitrogen compound biosynthetic process [inference]
organonitrogen compound metabolic process [inference]
biosynthetic process [inference]
cellular metabolic process [inference]
organic acid metabolic process [inference]
cellular aromatic compound metabolic process [inference]
nucleobase-containing compound metabolic process [inference]
aromatic compound biosynthetic process [inference]
phosphorus metabolic process [inference]
phosphate-containing compound metabolic process [inference]
organophosphate metabolic process [inference]
cellular nitrogen compound metabolic process [inference]
nucleobase-containing compound metabolic process [inference]
cellular nitrogen compound biosynthetic process [inference]
cellular biosynthetic process [inference]
heterocycle metabolic process [inference]
nucleobase-containing compound metabolic process [inference]
heterocycle biosynthetic process [inference]
primary metabolic process [inference]
small molecule metabolic process [inference]
organic substance metabolic process [inference]
organic acid metabolic process [inference]
lipid metabolic process [inference]
organophosphate metabolic process [inference]
carbohydrate derivative metabolic process [inference]
organic cyclic compound metabolic process [inference]
nucleobase-containing compound metabolic process [inference]
purine-containing compound metabolic process [inference]
organonitrogen compound metabolic process [inference]
organic substance biosynthetic process [inference]
cellular process [inference]
cellular metabolic process [inference]
organic acid metabolic process [inference]
cellular aromatic compound metabolic process [inference]
nucleobase-containing compound metabolic process [inference]
aromatic compound biosynthetic process [inference]
phosphorus metabolic process [inference]
phosphate-containing compound metabolic process [inference]
organophosphate metabolic process [inference]
cellular nitrogen compound metabolic process [inference]
nucleobase-containing compound metabolic process [inference]
cellular nitrogen compound biosynthetic process [inference]
cellular biosynthetic process [inference]
heterocycle metabolic process [inference]
nucleobase-containing compound metabolic process [inference]
heterocycle biosynthetic process [inference]
| GO Term | Evidence Code | PMID |
|---|---|---|
| nucleus | ||
| endoplasmic reticulum | ||
| endoplasmic reticulum membrane |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| oxidoreductase activity | ||
| very-long-chain-acyl-CoA dehydrogenase activity |
|
|
| protein binding | ||
| very-long-chain enoyl-CoA reductase activity |
GO Hierarchy
Human Protein Atlas
Tissue with high expression from Human Protein Atlas. Tissues that are highly expressed are highlighted.
KEGG BRITE Database
Rhea
Disease
- Disease Ontology
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0050889 | non-syndromic intellectual disability | |
| DOID:0060308 | autosomal recessive intellectual developmental disorder | |
| DOID:0060810 | syndromic X-linked intellectual disability type 10 | |
| DOID:0060823 | syndromic X-linked intellectual disability 94 | |
| DOID:0081188 | autosomal recessive intellectual developmental disorder 14 | |
| DOID:1059 | intellectual disability | |
| DOID:10907 | microcephaly | |
| DOID:114 | heart disease | |
| DOID:11832 | visual epilepsy | |
| DOID:12139 | dysthymic disorder |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0000007 | Autosomal recessive inheritance |
| HP:0000189 | Narrow palate |
| HP:0000750 | Delayed speech and language development |
| HP:0001249 | Intellectual disability |
| HP:0002080 | Intention tremor |
| HP:0003593 | Infantile onset |
| Disease ID | Disease Name |
|---|---|
| OMIM:614020 |
|
PubChem Disease
- MedGen Diseases
- OMIM Phenotypes
- KEGG Diseases
Ortholog
| Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
|---|---|---|---|
| 174140 | WB:WBGene00000198 | ||
| 38457 | FB:FBgn0035471 | ||
| 326954 | ZFIN:ZDB-GENE-030131-5154 | DANRE17169 | |
| 566085 | ZFIN:ZDB-GENE-090930-1 | ||
| 103047753 | ASTMX18469 | ||
| 100528865 | ICTPU21582 | ||
| 113592021 | ELEEL47763 | ||
| 115178551 | SALTR67782 | ||
| 115183312 | SALTR50872 | ||
| 100701654 | ORENI62395 |
