Gene Details | GeDiPNet - Complete Gene Info, Disease Associations & Pathways

Gene Gene SNPs miRNA Gene ontology Other IDs Protein Pathways Associated diseases
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.	9524
Gene name Gene Name - the full gene name approved by the HGNC.	Trans-2,3-enoyl-CoA reductase
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.	TECR
Synonyms (NCBI Gene) Gene synonyms aliases	GPSN2, MRT14, SC2, TER
Chromosome Chromosome number	19
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.	19p13.12
Summary Summary of gene provided in NCBI Entrez Gene.	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

Show/Hide all(1)

SNP ID	Visualize variation	Clinical significance	Consequence
rs199469705	C>T	Pathogenic	Missense variant, coding sequence variant, non coding transcript variant

Show/Hide all(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
MIRT1417786	hsa-miR-486-3p	CLIP-seq
MIRT2125403	hsa-miR-3184	CLIP-seq
MIRT2125404	hsa-miR-423-5p	CLIP-seq
MIRT2125405	hsa-miR-4656	CLIP-seq
MIRT2125406	hsa-miR-4663	CLIP-seq
MIRT2125407	hsa-miR-4715-3p	CLIP-seq
MIRT2347688	hsa-miR-1287	CLIP-seq
MIRT2347689	hsa-miR-185	CLIP-seq
MIRT2347690	hsa-miR-296-5p	CLIP-seq
MIRT2347691	hsa-miR-3135b	CLIP-seq
MIRT2347692	hsa-miR-361-3p	CLIP-seq
MIRT2347693	hsa-miR-4265	CLIP-seq
MIRT2347694	hsa-miR-4286	CLIP-seq
MIRT2347695	hsa-miR-4296	CLIP-seq
MIRT2347696	hsa-miR-4306	CLIP-seq
MIRT2347697	hsa-miR-4322	CLIP-seq
MIRT2347698	hsa-miR-4417	CLIP-seq
MIRT2347699	hsa-miR-4497	CLIP-seq
MIRT2347700	hsa-miR-4644	CLIP-seq
MIRT2347701	hsa-miR-4758-3p	CLIP-seq
MIRT2347702	hsa-miR-483-3p	CLIP-seq
MIRT2640570	hsa-miR-1909	CLIP-seq
MIRT2640571	hsa-miR-214	CLIP-seq
MIRT2125403	hsa-miR-3184	CLIP-seq
MIRT2640572	hsa-miR-339-3p	CLIP-seq
MIRT2640573	hsa-miR-3619-5p	CLIP-seq
MIRT2125404	hsa-miR-423-5p	CLIP-seq
MIRT2640574	hsa-miR-4291	CLIP-seq
MIRT2125405	hsa-miR-4656	CLIP-seq
MIRT2125406	hsa-miR-4663	CLIP-seq
MIRT2125407	hsa-miR-4715-3p	CLIP-seq
MIRT2640575	hsa-miR-4792	CLIP-seq
MIRT2640576	hsa-miR-761	CLIP-seq
MIRT2640577	hsa-miR-922	CLIP-seq
MIRT2640570	hsa-miR-1909	CLIP-seq
MIRT2640571	hsa-miR-214	CLIP-seq
MIRT2125403	hsa-miR-3184	CLIP-seq
MIRT2640572	hsa-miR-339-3p	CLIP-seq
MIRT2640573	hsa-miR-3619-5p	CLIP-seq
MIRT2125404	hsa-miR-423-5p	CLIP-seq
MIRT2640574	hsa-miR-4291	CLIP-seq
MIRT2125405	hsa-miR-4656	CLIP-seq
MIRT2125406	hsa-miR-4663	CLIP-seq
MIRT2125407	hsa-miR-4715-3p	CLIP-seq
MIRT2640575	hsa-miR-4792	CLIP-seq
MIRT2640576	hsa-miR-761	CLIP-seq
MIRT2640577	hsa-miR-922	CLIP-seq

Show/Hide all(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
GO:0005789	Component	Endoplasmic reticulum membrane	IDA	12482854
GO:0005789	Component	Endoplasmic reticulum membrane	IEA
GO:0005789	Component	Endoplasmic reticulum membrane	TAS
GO:0006629	Process	Lipid metabolic process	IEA
GO:0006631	Process	Fatty acid metabolic process	IEA
GO:0006633	Process	Fatty acid biosynthetic process	IEA
GO:0006665	Process	Sphingolipid metabolic process	IBA
GO:0006665	Process	Sphingolipid metabolic process	IEA
GO:0006665	Process	Sphingolipid metabolic process	IMP	25049234
GO:0016020	Component	Membrane	IEA
GO:0016491	Function	Oxidoreductase activity	IEA
GO:0016627	Function	Oxidoreductase activity, acting on the CH-CH group of donors	IEA
GO:0017099	Function	Very-long-chain fatty acyl-CoA dehydrogenase activity	TAS
GO:0030497	Process	Fatty acid elongation	IDA	12482854
GO:0035338	Process	Long-chain fatty-acyl-CoA biosynthetic process	TAS
GO:0042761	Process	Very long-chain fatty acid biosynthetic process	IBA
GO:0042761	Process	Very long-chain fatty acid biosynthetic process	IDA	12482854
GO:0042761	Process	Very long-chain fatty acid biosynthetic process	IMP	24220030
GO:0102758	Function	Very-long-chain enoyl-CoA reductase activity	IBA
GO:0102758	Function	Very-long-chain enoyl-CoA reductase activity	IDA	12482854
GO:0102758	Function	Very-long-chain enoyl-CoA reductase activity	IEA
GO:0102758	Function	Very-long-chain enoyl-CoA reductase activity	IMP	24220030

MIM	HGNC	e!Ensembl
610057	4551	ENSG00000099797

Protein

UniProt ID

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

	KEGG		Reactome
	Fatty acid elongation Biosynthesis of unsaturated fatty acids Metabolic pathways Fatty acid metabolism		Synthesis of very long-chain fatty acyl-CoAs

Show/Hide Unknown Diseases (2)

Disease merge term	Disease name	Evidence	References	Source
Unknown Includes: (1) ClinVar NON-pathogenic variants (Uncertain, Benign, Conflicting, VUS), (2) GenCC associations, (3) GWAS associations, (4) CBGDA evidence-based associations. NOTE: Diseases with pathogenic evidence are excluded to avoid conflicts.
Mental retardation	Intellectual disability, autosomal recessive 14, intellectual disability, autosomal recessive 14, intellectual disability	N/A	N/A	ClinVar, GenCC
Non-Syndromic Intellectual Disability	autosomal recessive non-syndromic intellectual disability	N/A	N/A	GenCC

Show/Hide Text Mining Associations (11)

Disease Name	Relationship Type	References
Associations from Text Mining Disease associations identified through Pubtator
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
Small Cell Lung Carcinoma	Associate	1645569

TECR (trans-2,3-enoyl-CoA reductase)