1. Gene
  2. VKORC1L1 - vitamin K epoxide reductase complex subunit 1 like 1 Gene

VKORC1L1 - vitamin K epoxide reductase complex subunit 1 like 1 Gene

Homo sapiens
Gene ID: 154807 | Gene type: protein coding

About VKORC1L1

Cytogenetic location: 7q11.21 Genomic coordinates (GRCh38): 7:65,865,772-65,959,558 (from NCBI)

This gene has 4 transcripts (splice variants), 205 orthologues and 1 paralogue. Ubiquitous expression in fat (RPKM 25.2), lung (RPKM 7.7) and 23 other tissues.

Summary

This gene encodes an Enzyme important in the vitamin K cycle, which is involved in the carboxylation of glutamate residues present in vitamin K-dependent proteins. The encoded Enzyme catalyzes the de-epoxidation of vitamin K 2,3-epoxide. Oxidative stress may upregulate expression of this gene and the encoded protein may protect cells and membrane proteins form oxidative damage. This gene and a related gene (Gene ID: 79001) may have arisen by gene duplication of an ancestral gene. [provided by RefSeq, Oct 2016]

VKORC1L1 Products(2)

mRNA Protein Name
NM_001284342.3 NP_001271271.1 vitamin K epoxide reductase complex subunit 1-like protein 1 isoform 2
NM_173517.6 NP_775788.2 vitamin K epoxide reductase complex subunit 1-like protein 1 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
32296183 GOA
enables vitamin-K-epoxide reductase (warfarin-sensitive) activity EXP
EXP: Inferred from Experiment
21367861 GOA
enables vitamin-K-epoxide reductase (warfarin-sensitive) activity IDA
IDA: Inferred from direct assay
21367861 GOA
Biological Process GO Annotation Evidence Reference Source
involved in cellular response to oxidative stress IMP
IMP: Inferred from mutant phenotype
21367861 GOA
involved in peptidyl-glutamic acid carboxylation IMP
IMP: Inferred from mutant phenotype
24532791 GOA
involved in vitamin K metabolic process IDA
IDA: Inferred from direct assay
21367861 GOA
Cellular Component GO Annotation Evidence Reference Source
located in endoplasmic reticulum membrane IDA
IDA: Inferred from direct assay
21367861 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

VKORC1L1 Protein Structure

VKOR

VKOR: Vitamin K epoxide reductase family (16 - 159)

  • 0
  • 100
  • 176 a.a.
Protein Preferred Names Protein Names

vitamin K epoxide reductase complex subunit 1-like protein 1

VKORC1-like protein 1

VKORC1L1 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method Reference
Intra
VKORC1L1 Q8N0U8 KLKB1 Homo sapiens P03952 32814053
Intra
VKORC1L1 Q8N0U8 KLKB1 Homo sapiens P03952 32814053
Intra
VKORC1L1 Q8N0U8 KLKB1 Homo sapiens P03952 32814053
Intra
VKORC1L1 Q8N0U8 CISD2 Homo sapiens Q8N5K1 32296183
Intra
VKORC1L1 Q8N0U8 CISD2 Homo sapiens Q8N5K1 32296183
Intra
VKORC1L1 Q8N0U8 CISD2 Homo sapiens Q8N5K1 32296183
Intra
VKORC1L1 Q8N0U8 GPX8 Homo sapiens Q8TED1 32296183
Intra
VKORC1L1 Q8N0U8 GPX8 Homo sapiens Q8TED1 32296183
Intra
VKORC1L1 Q8N0U8 GPX8 Homo sapiens Q8TED1 32296183
Intra
VKORC1L1 Q8N0U8 TMEM80 Homo sapiens Q96HE8 32296183
Intra
VKORC1L1 Q8N0U8 TMEM80 Homo sapiens Q96HE8 32296183
Intra
VKORC1L1 Q8N0U8 TMEM80 Homo sapiens Q96HE8 32296183
Intra
VKORC1L1 Q8N0U8 VHL Homo sapiens P40337-2 32814053
Intra
VKORC1L1 Q8N0U8 VHL Homo sapiens P40337-2 32814053
Intra
VKORC1L1 Q8N0U8 VHL Homo sapiens P40337-2 32814053
Intra
VKORC1L1 Q8N0U8 PCYT1B Homo sapiens Q9Y5K3-3 32296183
Intra
VKORC1L1 Q8N0U8 PCYT1B Homo sapiens Q9Y5K3-3 32296183
Intra
VKORC1L1 Q8N0U8 PCYT1B Homo sapiens Q9Y5K3-3 32296183
Intra
VKORC1L1 Q8N0U8 MS4A3 Homo sapiens Q96HJ5 32296183
Intra
VKORC1L1 Q8N0U8 MS4A3 Homo sapiens Q96HJ5 32296183
Intra
VKORC1L1 Q8N0U8 MS4A3 Homo sapiens Q96HJ5 32296183
Intra
VKORC1L1 Q8N0U8 AQP6 Homo sapiens Q13520 32296183
Intra
VKORC1L1 Q8N0U8 AQP6 Homo sapiens Q13520 32296183
Intra
VKORC1L1 Q8N0U8 PCYT1A Homo sapiens P49585 33961781
Intra
VKORC1L1 Q8N0U8 PCYT1A Homo sapiens P49585 32296183
Intra
VKORC1L1 Q8N0U8 PCYT1A Homo sapiens P49585 32296183
Intra
VKORC1L1 Q8N0U8 CCT2 Homo sapiens P78371 32814053
Intra
VKORC1L1 Q8N0U8 CCT2 Homo sapiens P78371 32814053
Intra
VKORC1L1 Q8N0U8 CCT2 Homo sapiens P78371 32814053
Intra
VKORC1L1 Q8N0U8 GORAB Homo sapiens Q5T7V8 32296183
Intra
VKORC1L1 Q8N0U8 GORAB Homo sapiens Q5T7V8 32296183
Intra
VKORC1L1 Q8N0U8 MTIF3 Homo sapiens Q9H2K0 32296183
Intra
VKORC1L1 Q8N0U8 MTIF3 Homo sapiens Q9H2K0 32296183
Intra
VKORC1L1 Q8N0U8 MTIF3 Homo sapiens Q9H2K0 32296183
Intra
VKORC1L1 Q8N0U8 MRM1 Homo sapiens Q6IN84 32296183
Intra
VKORC1L1 Q8N0U8 MRM1 Homo sapiens Q6IN84 32296183
Intra
VKORC1L1 Q8N0U8 LPL Homo sapiens P06858 32814053
Intra
VKORC1L1 Q8N0U8 LPL Homo sapiens P06858 32814053
Intra
VKORC1L1 Q8N0U8 LPL Homo sapiens P06858 32814053
Intra
VKORC1L1 Q8N0U8 AGT Homo sapiens P01019 32814053
Intra
VKORC1L1 Q8N0U8 AGT Homo sapiens P01019 32814053
Intra
VKORC1L1 Q8N0U8 AGT Homo sapiens P01019 32814053
Intra
VKORC1L1 Q8N0U8 ERGIC3 Homo sapiens Q9Y282 32296183
Intra
VKORC1L1 Q8N0U8 ERGIC3 Homo sapiens Q9Y282 32296183
Intra
VKORC1L1 Q8N0U8 ERGIC3 Homo sapiens Q9Y282 32296183
Cross: Cross-species interaction Intra: Intraspecies interaction

Related Diseases

Diseases Alias
Coumarin Resistance

Warfarin Resistance

Warfarin Sensitivity

Coumadin Sensitivity

Warfarin Response

Poor Metabolism Of Coumarin

Coumarin, Poor Metabolism Of

CMRES

Hereditary Combined Deficiency Of Vitamin K-Dependent Clotting Factors

Hereditary Combined Deficiency Of Factors Ii, Vii, Ix And X

Vkcfd

Vitamin K-Dependent Clotting Factors, Combined Deficiency Of, 2

VKCFD2

Combined Deficiency Of Vitamin K-Dependent Clotting Factors 2

Vitamin K-Dependent Clotting Factors, Combined Deficiency Of, Type 2

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
Mus musculus VKORC1L1 MGD MGI:1916818
Canis familiaris VKORC1L1 VGNC VGNC:82304
Rattus norvegicus VKORC1L1 RGD RGD:1303249
Bos taurus VKORC1L1 VGNC VGNC:58426
Macaca mulatta VKORC1L1 VGNC VGNC:79322