Gene Gene information from NCBI Gene database.
Entrez ID 9524
Gene name Trans-2,3-enoyl-CoA reductase
Gene symbol TECR
Synonyms (NCBI Gene)
GPSN2MRT14SC2TER
Chromosome 19
Chromosome location 19p13.12
Summary This gene encodes a multi-pass membrane protein that resides in the endoplasmic reticulum, and belongs to the steroid 5-alpha reductase family. The elongation of microsomal long and very long chain fatty acid consists of 4 sequential reactions. This prote
SNPs SNP information provided by dbSNP.
1
SNP ID Visualize variation Clinical significance Consequence
rs199469705 C>T Pathogenic Missense variant, coding sequence variant, non coding transcript variant
miRNA miRNA information provided by mirtarbase database.
52
miRTarBase ID miRNA Experiments Reference
MIRT016309 hsa-miR-193b-3p Proteomics 21512034
MIRT040058 hsa-miR-615-3p CLASH 23622248
MIRT040058 hsa-miR-615-3p CLASH 23622248
MIRT037695 hsa-miR-744-5p CLASH 23622248
MIRT1417785 hsa-miR-3937 CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
27
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 25416956, 30021884, 32296183, 38422897
GO:0005634 Component Nucleus HDA 21630459
GO:0005783 Component Endoplasmic reticulum IBA
GO:0005783 Component Endoplasmic reticulum IDA 24220030
GO:0005783 Component Endoplasmic reticulum IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
610057 4551 ENSG00000099797
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q9NZ01
Protein name Very-long-chain enoyl-CoA reductase (EC 1.3.1.93) (Synaptic glycoprotein SC2) (Trans-2,3-enoyl-CoA reductase) (TER)
Protein function Involved in both the production of very long-chain fatty acids for sphingolipid synthesis and the degradation of the sphingosine moiety in sphingolipids through the sphingosine 1-phosphate metabolic pathway (PubMed:25049234). Catalyzes the last
PDB 2DZJ
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF02544 Steroid_dh 154 308 3-oxo-5-alpha-steroid 4-dehydrogenase Family
Tissue specificity TISSUE SPECIFICITY: Expressed in most tissues tested. Highly expressed in skeletal muscle. {ECO:0000269|PubMed:12482854}.
Sequence
MKHYEVEILDAKTREKLCFLDKVEPHATIAEIKNLFTKTHPQWYPARQSLRLDPKGKSLK
DEDVLQKLPVGTTATLYFRDLGAQISWVTVFLTEYAGPLFIYLLFYFRVPFIYGHKYDFT
SSRHTVVHLACICHSFHYIKRLLETLFVHRFSHGTMPLRNIFKNCTYYWGFAAWMAYYIN
HPLYTPPTYGAQQVKLALAIFVICQLGNFSIHMALRDLRPAGSKTRKIPYPTKNPFTWLF
LLVSCPNYTYEVGSWIGFAIMTQCLPVALFSLVGFTQMTIWAKGKHRSYLKEFRDYPPLR
MPIIPFLL
Sequence length 308
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG  Reactome
  Fatty acid elongation
Biosynthesis of unsaturated fatty acids
Metabolic pathways
Fatty acid metabolism
  Synthesis of very long-chain fatty acyl-CoAs
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
13
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Colon adenocarcinoma Uncertain significance rs767614261 RCV005937404
Gastric cancer Uncertain significance rs767614261 RCV005937405
Intellectual disability, autosomal recessive 14 Uncertain significance; Benign; Likely benign; no classifications from unflagged records rs772297819, rs113855270, rs753690636, rs199469705 RCV001330353
RCV002500596
RCV001335398
RCV000023795
TECR-related disorder Likely benign; Benign rs563957558, rs76484116, rs59273619, rs10405483, rs1220920046, rs776703090 RCV003952092
RCV003925159
RCV003915175
RCV003925160
RCV003981989
RCV003957192
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
Carcinoma Non Small Cell Lung Associate 1645569
Colorectal Neoplasms Associate 35779418
COVID 19 Associate 36941056
Hemolysis Associate 31246487
Intellectual Disability Associate 21212097, 22419660
Mental Retardation Autosomal Recessive 4 Associate 21212097
Mental Retardation X Linked Nonsyndromic Associate 24220030
Neoplasms Associate 18593932
Obesity Associate 35779418
Sarcoma Kaposi Associate 40016701