1. Gene
  2. TECR - trans-2,3-enoyl-CoA reductase Gene

TECR - trans-2,3-enoyl-CoA reductase Gene

Homo sapiens

Also known as SC2; TER; GPSN2; MRT14

Gene ID: 9524 | Gene type: protein coding

About TECR

Cytogenetic location: 19p13.12 Genomic coordinates (GRCh38): 19:14,527,726-14,565,980 (from NCBI)

This gene has 26 transcripts (splice variants), 268 orthologues, 3 paralogues and is associated with 2 phenotypes. Ubiquitous expression in esophagus (RPKM 95.3), skin (RPKM 93.5) and 25 other tissues.

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 protein catalyzes the final step, reducing trans-2,3-enoyl-CoA to saturated acyl-CoA. Alternatively spliced transcript variants have been found for this gene.[provided by RefSeq, Apr 2011]

TECR Products(2)

mRNA Protein Name
NM_001321170.1 NP_001308099.1 very-long-chain enoyl-CoA reductase isoform 2
NM_138501.6 NP_612510.1 very-long-chain enoyl-CoA reductase isoform 1
Gene Ontology
  • Molecular Function
  • Biological Process
  • Cellular Component
Molecular Function GO Annotation Evidence Reference Source
enables protein binding IPI
IPI: Inferred from physical interaction
25416956 GOA
enables very-long-chain enoyl-CoA reductase activity IDA
IDA: Inferred from direct assay
12482854 GOA
enables very-long-chain enoyl-CoA reductase activity IMP
IMP: Inferred from mutant phenotype
24220030 GOA
Biological Process GO Annotation Evidence Reference Source
involved in fatty acid elongation IDA
IDA: Inferred from direct assay
12482854 GOA
involved in sphingolipid metabolic process IMP
IMP: Inferred from mutant phenotype
25049234 GOA
involved in very long-chain fatty acid biosynthetic process IDA
IDA: Inferred from direct assay
12482854 GOA
involved in very long-chain fatty acid biosynthetic process IMP
IMP: Inferred from mutant phenotype
24220030 GOA
Cellular Component GO Annotation Evidence Reference Source
located in endoplasmic reticulum IDA
IDA: Inferred from direct assay
24220030 GOA
located in endoplasmic reticulum membrane IDA
IDA: Inferred from direct assay
12482854 GOA
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern

TECR Protein Structure

Steroid_dh

Steroid_dh: 3-oxo-5-alpha-steroid 4-dehydrogenase (155 - 308)

  • 0
  • 100
  • 200
  • 308 a.a.
Protein Preferred Names Protein Names

very-long-chain enoyl-CoA reductase

epididymis secretory sperm binding protein

TECR Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method Reference
Intra
TECR Q9NZ01 RETREG3 Homo sapiens Q86VR2 32296183
Intra
TECR Q9NZ01 RETREG3 Homo sapiens Q86VR2 32296183
Intra
TECR Q9NZ01 JAGN1 Homo sapiens Q8N5M9 32296183
Intra
TECR Q9NZ01 JAGN1 Homo sapiens Q8N5M9 32296183
Intra
TECR Q9NZ01 TFAM Homo sapiens Q00059 32296183
Intra
TECR Q9NZ01 TFAM Homo sapiens Q00059 32296183
Intra
TECR Q9NZ01 PGRMC2 Homo sapiens O15173 32296183
Intra
TECR Q9NZ01 PGRMC2 Homo sapiens O15173 32296183
Intra
TECR Q9NZ01 VMA21 Homo sapiens Q3ZAQ7 32296183
Intra
TECR Q9NZ01 VMA21 Homo sapiens Q3ZAQ7 32296183
Intra
TECR Q9NZ01 ARL13B Homo sapiens Q3SXY8 32296183
Intra
TECR Q9NZ01 ARL13B Homo sapiens Q3SXY8 32296183
Intra
TECR Q9NZ01 HACD1 Homo sapiens B0YJ81 32296183
Intra
TECR Q9NZ01 HACD1 Homo sapiens B0YJ81 32296183
Intra
TECR Q9NZ01 STOM Homo sapiens P27105 32296183
Intra
TECR Q9NZ01 STOM Homo sapiens P27105 32296183
Intra
TECR Q9NZ01 GOLT1A Homo sapiens Q6ZVE7 32296183
Intra
TECR Q9NZ01 GOLT1A Homo sapiens Q6ZVE7 32296183
Intra
TECR Q9NZ01 CRB3 Homo sapiens Q9BUF7-2 32296183
Intra
TECR Q9NZ01 CRB3 Homo sapiens Q9BUF7-2 32296183
Intra
TECR Q9NZ01 MUC1 Homo sapiens P15941-11 32296183
Intra
TECR Q9NZ01 MUC1 Homo sapiens P15941-11 32296183
Intra
TECR Q9NZ01 SLC10A6 Homo sapiens Q3KNW5 32296183
Intra
TECR Q9NZ01 SLC10A6 Homo sapiens Q3KNW5 32296183
Intra
TECR Q9NZ01 FAM209A Homo sapiens Q5JX71 32296183
Intra
TECR Q9NZ01 FAM209A Homo sapiens Q5JX71 32296183
Intra
TECR Q9NZ01 CLDN5 Homo sapiens O00501 32296183
Intra
TECR Q9NZ01 CLDN5 Homo sapiens O00501 32296183
Intra
TECR Q9NZ01 ELOVL4 Homo sapiens Q9GZR5 32296183
Intra
TECR Q9NZ01 ELOVL4 Homo sapiens Q9GZR5 32296183
Intra
TECR Q9NZ01 GET1 Homo sapiens O00258 32296183
Intra
TECR Q9NZ01 GET1 Homo sapiens O00258 32296183
Intra
TECR Q9NZ01 STING1 Homo sapiens Q86WV6 32296183
Intra
TECR Q9NZ01 STING1 Homo sapiens Q86WV6 32296183
Intra
TECR Q9NZ01 MFSD14B Homo sapiens Q5SR56 32296183
Intra
TECR Q9NZ01 MFSD14B Homo sapiens Q5SR56 32296183
Intra
TECR Q9NZ01 SLC7A14 Homo sapiens Q8TBB6 32296183
Intra
TECR Q9NZ01 SLC7A14 Homo sapiens Q8TBB6 32296183
Intra
TECR Q9NZ01 HACD2 Homo sapiens Q6Y1H2 30021884
Intra
TECR Q9NZ01 HACD2 Homo sapiens Q6Y1H2 25416956
Intra
TECR Q9NZ01 HACD2 Homo sapiens Q6Y1H2 25416956
Intra
TECR Q9NZ01 HACD2 Homo sapiens Q6Y1H2 25416956
Intra
TECR Q9NZ01 MMGT1 Homo sapiens Q8N4V1 32296183
Intra
TECR Q9NZ01 MMGT1 Homo sapiens Q8N4V1 32296183
Intra
TECR Q9NZ01 CREB3L1 Homo sapiens Q96BA8 32296183
Intra
TECR Q9NZ01 CREB3L1 Homo sapiens Q96BA8 32296183
Intra
TECR Q9NZ01 CD79A Homo sapiens P11912 32296183
Intra
TECR Q9NZ01 CD79A Homo sapiens P11912 32296183
Intra
TECR Q9NZ01 ERGIC3 Homo sapiens Q9Y282 32296183
Intra
TECR Q9NZ01 ERGIC3 Homo sapiens Q9Y282 32296183
Intra
TECR Q9NZ01 ERGIC3 Homo sapiens Q9Y282 32296183
Cross: Cross-species interaction Intra: Intraspecies interaction

Related Diseases

Diseases Alias
Intellectual Developmental Disorder, Autosomal Recessive 14

MRT14

Mental Retardation, Autosomal Recessive 14

Autosomal Recessive Intellectual Developmental Disorder 14

Mental Retardation, Autosomal Recessive, Type 14

Autosomal Recessive Non-Syndromic Intellectual Disability

Ar-Nsid

Ns-Arid

Seborrheic Infantile Dermatitis

Cradle Cap

Infantile Seborrhoeic Dermatitis

Seborrhoea Capitis

Seborrhoeic Dermatitis Of Scalp

Seborrhoeic Eczema Of Scalp

Complement 5 Dysfunction

Generalized Seborrheic Dermatitis Of Infants

Infantile Seborrheic Dermatitis

Pityriasis Capitis

Seborrhea Capitis

Seborrhea Sicca

Dandruff

Complement Component 5 Deficiency

Seborrheic Dermatitis

Seborrheic Dermatitis Of Scalp

Scurfiness Of Scalp

Seborrheic Dermatitis Of Infancy

Infantile Seborrhoeic Eczema

Neonatal Seborrhoeic Dermatitis

Infantile Seborrhoeic Dermatitis Of The Scalp

Cataract 24

CTRCT24

Cataract 24, Anterior Polar

Cataract, Anterior Polar, 2

Ctaa2

Anterior Polar Cataract 2

Early-Onset Anterior Polar Cataract

Early-Onset Anterior Subcapsular Cataract

Anterior Polar Cataract 24

Cataract Anterior Polar

Cataract, Anterior Polar-2

Cataract, Anterior Polar

Tongue Carcinoma

Tongue Cancer

Malignant Neoplasm Of Tongue

Tongue Neoplasms

Tongue Neoplasm

Oral Mucosa Leukoplakia

Leukoplakia, Oral

Leukoplakia Of Buccal Mucosa

Spindle Cell Hemangioma

Sch

Spindle Cell Hemangioendothelioma

Autosomal Recessive Intellectual Developmental Disorder

Mental Retardation, Autosomal Recessive

Autosomal Recessive Mental Retardation

Autosomal Recessive Non-Syndromic Mental Retardation

Autosomal Recessive Non-Syndromic Intellectual Disability

Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Orthologs Information

Species Symbol Source ID
Felis catus TECR VGNC VGNC:80732
Macaca mulatta TECR VGNC VGNC:103877
Canis familiaris TECR VGNC VGNC:47234
Rattus norvegicus TECR RGD RGD:620376
Bos taurus TECR VGNC VGNC:35730
Mus musculus TECR MGD MGI:1915408