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Category   Symbol Source: HGNC EntrezGene Ensembl GeneCards RNA genes CroW21
GIFtS

NQO2 Gene

protein-coding   GIFtS: 60
GCID: GC06P003000

NAD(P)H dehydrogenase, quinone 2

(Previous names: NAD(P)H menadione oxidoreductase 2, dioxin-inducible )
(Previous symbol: NMOR2)
 Explore 22 diseases affiliated with
NQO2 via our new
 Human Malady Compendium 
Biological research products
for NQO2
    

(According to 1HGNC, 2Entrez Gene,
3UniProtKB/Swiss-Prot, 4UniProtKB/TrEMBL, 5OMIM, 6GeneLoc, 7Ensembl, 8DME, 9miRBase, and/or 10fRNAdb)
About This Section

Aliases
NAD(P)H Dehydrogenase, Quinone 21 2     NRH Dehydrogenase [Quinone] 22 3
NMOR21 2 3 5     NRH:Quinone Oxidoreductase 22 3
QR21 2 3     NAD(P)H Menadione Oxidoreductase-1, Dioxin-Inducible-22
DHQV1 2     Ribosyldihydronicotinamide Dehydrogenase2
DIA61 2     Ribosyldihydronicotinamide Dehydrogenase [Quinone]2
NAD(P)H Menadione Oxidoreductase 2, Dioxin-Inducible1 2     EC 1.10.99.23
Quinone Reductase 22 3     

External Ids:    HGNC: 78561   Entrez Gene: 48352   Ensembl: ENSG000001245887   OMIM: 1609985   UniProtKB: P160833   

Export aliases for NQO2 gene to outside databases

Previous GC identifers: GC06P002985 GC06P002945 GC06P002873


(According to Entrez Gene, Tocris Bioscience, Wikipedia's Gene Wiki, PharmGKB,
UniProtKB/Swiss-Prot, and/or UniProtKB/TrEMBL)
About This Section

Entrez Gene summary for NQO2:
NQO2 (EC 1.10.99.2) is a flavoprotein that catalyzes the 2-electron reduction of various quinones, redox dyes, and the
vitamin K menadione. NQO2 predominantly uses dihydronicotinamide riboside (NRH) as the electron donor (summary by Wu
et al., 1997 (PubMed 9367528)).(supplied by OMIM, Jul 2010)

UniProtKB/Swiss-Prot: NQO2_HUMAN, P16083
Function: The enzyme apparently serves as a quinone reductase in connection with conjugation reactions of hydroquinones
involved in detoxification pathways as well as in biosynthetic processes such as the vitamin K-dependent
gamma-carboxylation of glutamate residues in prothrombin synthesis

Gene Wiki entry for NQO2


(According to GeneLoc and/or HGNC, and/or
Entrez Gene (NCBI build 37),
and/or miRBase,
Genomic Views according to UCSC (hg19) and Ensembl (release 69), Regulatory elements and Epigenetics data according to QIAGEN, SABiosciences, and/or SwitchGear Genomics)
About This Section
RefSeq DNA sequence:
NC_000006.11  NC_018917.1  NT_007592.15  
Regulatory elements:
   SABiosciences Regulatory transcription factor binding sites in the NQO2 gene promoter:
         Sp1   AP-1   ATF-2   c-Jun   C/EBPalpha   
         Other transcription factors

SwitchGear Promoter luciferase reporter plasmidNQO2 promoter sequence
   Search SABiosciences Chromatin IP Primers for NQO2

Epigenetics:
QIAGEN PyroMark CpG Assay predesigned Pyrosequencing DNA Methylation assays in human, mouse, rat NQO2


Genomic Location:
Genomic View: UCSC Golden Path with GeneCards custom track

Entrez Gene cytogenetic band: 6p25.2   Ensembl cytogenetic band:  6p25.2   HGNC cytogenetic band: 6p25.2

NQO2 Gene in genomic location: bands according to Ensembl, locations according to (and/or Entrez Gene and/or Ensembl if different)
NQO2 gene location

GeneLoc information about chromosome 6         GeneLoc Exon Structure

GeneLoc location for GC06P003000:  view genomic region     (about GC identifiers)

Start:
2,988,221 bp from pter      End:
3,019,996 bp from pter
Size:
31,776 bases      Orientation:
plus strand

(According to 1UniProtKB, HORDE, neXtProt, Ensembl, and/or Reactome, Modification sites according to 2PhosphoSitePlus, Specific Peptides from DME, Protein expression images according to data from SPIRE MOPED and PaxDb, RefSeq according to NCBI, PDB rendering according to OCA and/or Proteopedia, Recombinant Proteins from EMD Millipore, R&D Systems, GenScript, Enzo Life Sciences, OriGene, Novus Biologicals, Sino Biological, ProSpec, and/or Uscn,
Biochemical Assays by EMD Millipore, R&D Systems, OriGene, GenScript, Cell Signaling Technology, Enzo Life Sciences, and/or Uscn, Ontologies according to Gene Ontology Consortium 01 Mar 2013 and Entrez Gene, Antibodies by EMD Millipore, R&D Systems, GenScript, Cell Signaling Technology, OriGene, Novus Biologicals, Thermo Fisher Scientific, Abcam, and/or Uscn)
About This Section

UniProtKB/Swiss-Prot: NQO2_HUMAN, P16083 (See protein sequence)
Recommended Name: Ribosyldihydronicotinamide dehydrogenase [quinone]  
Size: 231 amino acids; 25919 Da
Cofactor: Binds 1 zinc ion per subunit
Cofactor: FAD
Subunit: Homodimer
Subcellular location: Cytoplasm
Miscellaneous: Uses dihydronicotinamide riboside (NRH) rather than NAD(P)H as an electron donor
6/40 PDB 3D structures from and Proteopedia for NQO2 (see all 40):
1QR2 (3D)        1SG0 (3D)        1XI2 (3D)        1ZX1 (3D)        2BZS (3D)        2QMY (3D)    
Secondary accessions: B2R492 Q5TD04

Explore the universe of human proteins at neXtProt for NQO2: NX_P16083

Post-translational modifications:

  • View modification sites using PhosphoSitePlus2
  • View neXtProt modification sites for NX_P16083

  • NQO2 Protein expression data from MOPED and PaxDb:    About this image 
    Estimated protein expression log10 (pmol).

    REFSEQ proteins: NP_000895.2  
    ENSEMBL proteins: 
     ENSP00000406951   ENSP00000369839   ENSP00000380829   ENSP00000337773   ENSP00000369806  
     ENSP00000369822   ENSP00000369821   ENSP00000369795  

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    Uscn Proteins for NQO2

    Gene Ontology (GO): 3 cellular component terms (GO ID links to tree view):    About this table

    GO IDQualified GO termEvidencePubMed IDs
    GO:0005634nucleus IDA--
    GO:0005730NOT nucleolus IDA--
    GO:0005737cytoplasm IDA--


    NQO2 for ontologies           About GeneDecksing



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    (According to InterPro, ProtoNet, UniProtKB, and/or BLOCKS, Sets of similar genes according to GeneDecks)
    About This Section

    NQO2 for domains           About GeneDecksing

    1 InterPro domain/family:
     IPR003680 Flavodoxin_fold

    Graphical View of Domain Structure for InterPro Entry P16083

    ProtoNet protein and cluster: P16083

    1 Blocks protein family: IPB003680 NAD(P)H dehydrogenase (quinone)

    UniProtKB/Swiss-Prot: NQO2_HUMAN, P16083
    Similarity: Belongs to the NAD(P)H dehydrogenase (quinone) family


    (According to 1UniProtKB, Genatlas, LifeMap Discovery™, IUBMB, and/or 2DME, Human phenotypes from GenomeRNAi, Animal models from MGI Mar 06 2013,
    bound targets from SABiosciences, miRNA Gene Targets from miRTarBase shRNA from OriGene, RNAi from EMD Millipore, siRNAs from OriGene, QIAGEN, microRNA from QIAGEN, Gene Editing from DNA2.0, Clones from EMD Millipore, OriGene, SwitchGear Genomics, GenScript, Sino Biological, DNA2.0, and Vector BioLabs, Cell Lines from GenScript, LifeMap BioReagents, In Situ Hybridization Assays from Advanced Cell Diagnostics, Ontologies according to Gene Ontology Consortium 01 Mar 2013 via Entrez Gene.)
    About This Section

    Function Summary:

         UniProtKB/Swiss-Prot: NQO2_HUMAN, P16083
    Function: The enzyme apparently serves as a quinone reductase in connection with conjugation reactions of hydroquinones
    involved in detoxification pathways as well as in biosynthetic processes such as the vitamin K-dependent
    gamma-carboxylation of glutamate residues in prothrombin synthesis
    Catalytic activity: 1-(beta-D-ribofuranosyl)-1,4-dihydronicotinamide + a quinone = 1-(beta-D-ribofuranosyl)nicotinamide
    + a hydroquinone
    Enzyme regulation: Inhibited by melatonin, resveratrol and 5-hydroxytryptamine
    Biophysicochemical properties: Kinetic parameters: KM=28 uM for NRH; KM=11.6 uM for menadione; KM=252 uM for NADH;

    Enzyme Number (IUBMB): EC 1.10.99.21

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    Gene Ontology (GO): 4 molecular function terms (GO ID links to tree view):    About this table

    GO IDQualified GO termEvidencePubMed IDs
    GO:0001512dihydronicotinamide riboside quinone reductase activity IEA--
    GO:0008753NADPH dehydrogenase (quinone) activity TAS1691923
    GO:0009055electron carrier activity TAS1691923
    GO:0046872metal ion binding IEA--


    NQO2 for ontologies           About GeneDecksing


    1 GenomeRNAi human phenotype for NQO2:
     Synthetic lethal with Ras 

    Animal Models:
         Mouse knock-outs for NQO2: Nqo2tm1Akj Nqo2tm1Bout
         7 MGI mutant phenotypes (inferred from 2 alleles(MGI details for Nqo2):
     behavior/neurological  cellular  hematopoietic system  homeostasis/metabolism  immune system 
     integument  tumorigenesis 

    NQO2 for phenotypes           About GeneDecksing


    (Pathways according to EMD Millipore, R&D Systems, Cell Signaling Technology, KEGG, PharmGKB, BioSystems, Reactome, Tocris Bioscience, GeneGo (Thomson Reuters), QIAGEN, and/or UniProtKB, Sets of similar genes according to GeneDecks, Interaction Networks according to SABiosciences, and/or STRING, Interactions according to 1UniProtKB, 2MINT, 3I2D, and/or 4STRING, with links to IntAct and Ensembl, Ontologies according to Gene Ontology Consortium 01 Mar 2013 via Entrez Gene).
    About This Section



    Interactions:

        SABiosciences Gene Network CentralTM Interacting Genes and Proteins Network for NQO2

    STRING Interaction Network Preview (showing 5 interactants - click image to see more details)

    5/7 Interacting proteins for NQO2 (P160832, 3 ENSP000003377734) via UniProtKB, MINT, STRING, and/or I2D (see all 7)
    InteractantInteraction Details
    GeneCardExternal ID(s)
    RELBQ012012, 3MINT-49032 I2D: score=2 
    RHOBP627453, ENSP000002722334I2D: score=2 STRING: ENSP00000272233
    TP53P046373, ENSP000002693054I2D: score=1 STRING: ENSP00000269305
    GORASP2Q9H8Y83, ENSP000002341604I2D: score=4 STRING: ENSP00000234160
    MAGEA11P433643I2D: score=1 
    About this table

    Gene Ontology (GO): 1 biological process term (GO ID links to tree view):    About this table

    GO IDQualified GO termEvidencePubMed IDs
    GO:0007613memory IEA--


    NQO2 for ontologies           About GeneDecksing



    (Chemical Compounds according to UniProtKB, Enzo Life Sciences, EMD Millipore, Tocris Bioscience HMDB, BitterDB, and/or Novoseek, and Drugs according to DrugBank, Enzo Life Sciences, and/or PharmGKB, with drugs/clinical trials/news search links to CenterWatch)
    About This Section

    NQO2 for compounds           About GeneDecksing

    Browse Small Molecules at EMD Millipore
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    Browse Tocris compounds for NQO2

    7 HMDB Compounds for NQO2    About this table
    CompoundSynonyms CAS #PubMed Ids
    1-(beta-D-Ribofuranosyl)-1,4-dihydronicotinamideReduced nicotinamide riboside (see all 3)----
    FAD1H-Purin-6-amine flavin dinucleotide (see all 21)146-14-5--
    Hydroquinone1,4-Benzenediol (see all 35)123-31-9--
    MenadioneVitamin K3: 1,4-Dihydro-1,4-dioxo-2-methylnaphthalene (see all 49)58-27-5--
    NAD3-Carbamoyl-1-D-ribofuranosylpyridinium hydroxide 5'-ester with adenosine 5'-pyrophosphate (see all 28)53-84-9--
    Nicotinamide riboside1-b-D-ribosyl-3-Pyridinecarboxamide (see all 12)1341-23-7--
    Quinone1,4-Benzoquine (see all 25)106-51-4--

    10/12 DrugBank Compounds for NQO2 (see all 12)    About this table
    CompoundSynonyms CAS #TypeActionsPubMed Ids
    Menadione2-Methyl-1,4-Naphthalenedione (see all 7)58-27-5target--15078100 12351651 16765324 15733542 10433694
    Flavin-Adenine Dinucleotide-- 146-14-5target--17139284 17016423
    NADHbeta-DPNH (see all 18)606-68-8target--17031400 16905546
    Resveratrol(E)-5-(2-(4-hydroxyphenyl)ethenyl)-1,3-benzenediol (see all 9)501-36-0target--15350128 15381063
    (3S)-3-hydroxy-1-methyl-2,3-dihydro-1H-indole-5,6-dione-- --target--10592235
    10-Propargyl-5,8-Dideazafolic Acid-- --target--10592235
    5,8-dimethoxy-1,4-dimethylquinolin-2(1H)-one-- --target--10592235
    6-methoxy-9-methyl[1,3]dioxolo[4,5-h]quinolin-8(9H)-one-- --target--10592235
    CB1954-- --target--10592235
    MelatoninMEL (see all 4)73-31-4target--19463840

    10/21 Novoseek chemical compound relationships for NQO2 gene (see all 21)    About this table
    Compound   -log (P-Val)   Hits   PubMed IDs for Articles with Shared Sentences (# sentences)
    quinone 91.6 99 18579530 (7), 15733542 (5), 15350128 (3), 18254726 (3) (see all 52)
    cb1954 87.4 6 16129418 (2), 18062662 (2), 9367528 (1)
    menadione 75.7 7 18374191 (1), 15733542 (1), 1691923 (1), 18254726 (1) (see all 6)
    melatonin 68.7 46 18254726 (5), 17910598 (4), 16293234 (3), 18502195 (2) (see all 14)
    2[125i]iodomelatonin 68.1 3 18254726 (1)
    dicoumarol 63 3 11154737 (1), 9367528 (1)
    tbhq 57.6 3 16545679 (2)
    resveratrol 54.8 30 18671725 (7), 15350128 (5), 15993843 (3), 19767760 (2)
    beta-naphthoflavone 45 2 8182056 (1)
    nadph 44.5 6 11154737 (1), 18538895 (1), 9050836 (1), 17031400 (1) (see all 6)

    Search CenterWatch for drugs/clinical trials and news about NQO2 

    (Secondary structures according to fRNAdb,
    GenBank/EMBL/DDBJ Accessions according to
    Unigene (Build 235 Homo sapiens; Mar 10 2013) or GenBank,
    RefSeq according to Entrez Gene,
    DOTS (version 10), and/or AceView, transcript ids from Ensembl with links to UCSC,
    exon structure from GeneLoc, alternative splicing isoforms according to ASD and/or ECgene,
    RNAi Products from EMD Millipore,
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    Tagged/untagged cDNA clones from OriGene, SwitchGear Genomics, GenScript, DNA2.0, Vector BioLabs, Primers from OriGene, SABiosciences, and/or QIAGEN )
    About This Section

    REFSEQ mRNAs for NQO2 gene: 
    NM_000904.3  

    Unigene Clusters for NQO2:

    NAD(P)H dehydrogenase, quinone 2
    Hs.145597  [show with all ESTs], Hs.533050  [show with all ESTs]
    Unigene Representative Sequences: AK097187, AK056981
    8 Ensembl transcripts including schematic representations, and UCSC links where relevant:
    ENST00000426637 ENST00000380472(uc003mup.1) ENST00000397717 ENST00000338130(uc003mus.2 uc003mut.2)
    ENST00000380441 ENST00000380455 ENST00000380454 ENST00000380430

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    Additional cDNA sequence: 

    AK056981.1 AK311746.1 BC006096.2 J02888.1 

    17 DOTS entries:

    DT.452875  DT.100797292  DT.100017506  DT.65284171  DT.97847745  DT.95173411  DT.100797286  DT.102827444 
    DT.121352982  DT.216153  DT.100683819  DT.92426442  DT.92426448  DT.98083451  DT.99997381  DT.65284170 
    DT.91654768 

    24/260 AceView cDNA sequences (see all 260):

    BU607941 BQ184931 AK056981 BQ185566 CA310341 BF689694 CN479098 BM683654 
    CK300956 BX280672 CD369046 BQ226005 BU626474 BQ025114 AI216650 CD366005 
    CR600371 BM683688 BM824959 CA308279 BM798996 BM984758 AW005149 AI492470 

    GeneLoc Exon Structure

    5/8 Alternative Splicing Database (ASD) splice patterns (SP) for NQO2 (see all 8)    About this scheme

    ExUns: 1a · 1b · 1c ^ 2 ^ 3 ^ 4a · 4b ^ 5 ^ 6 ^ 7a · 7b ^ 8a · 8b ^ 9a · 9b ^ 10 ^ 11a · 11b
    SP1:                    -                 -                                                                     
    SP2:                    -     -     -     -     -                                                               
    SP3:                    -     -     -     -     -                                   -     -                     
    SP4:                          -     -     -     -                                                               
    SP5:                    -     -     -     -     -           -     -                                             


    ECgene alternative splicing isoforms for NQO2

    (RNA expression data according to H-InvDB, NONCODE, miRBase, and RNAdb, Expression images according to data from BioGPS, Illumina Human BodyMap, and CGAP SAGE, Sets of similar genes according to GeneDecks, in vivo and in vitro expression data from LifeMap Discovery™, plus additional links to Genevestigator, and/or SOURCE, and/or BioGPS, and/or UniProtKB,
    PCR Arrays from SABiosciences, Primers from OriGene, SABiosciences, and/or QIAGEN, In Situ Hybridization Assays from Advanced Cell Diagnostics)
    About This Section

    NQO2 expression in normal human tissues (normalized intensities)
    See probesets specificity/sensitivity at GeneAnnot
    About this imageBioGPS
    CGAP TAG: CAGAGACTTT

    Microarray
    RNAseq (Illumina Body Map)
    (100×FPKM)½
    SAGE (Serial Analysis of Gene Expression)

    About this image
    See NQO2 Protein Expression from SPIRE MOPED and PaxDB
    Genevestigator expression for NQO2

    SOURCE GeneReport for Unigene clusters: Hs.145597 Hs.533050
        SABiosciences Expression via Pathway-Focused PCR Array including NQO2: 
              Drug Metabolism: Phase II Enzymes in human mouse rat

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    In Situ
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    (Orthologs according to 1,2HomoloGene (2older version, for species not in 1newer version), 3euGenes, 4SGD , 5MGI Mar 06 2013, with possible further links to Flybase and/or WormBase, and/or 6Ensembl pan taxonomic compara , Gene Trees according to Ensembl and TreeFam)
    About This Section

    This gene was present in the last universal common ancestor (LUCA).

    Orthologs for NQO2 gene from 6/12 species (see all 12)    About this table
    Organism Taxonomic
    classification
    Gene Description Human
    Similarity
    Orthology
    Type
    Details
    mouse
    (Mus musculus)
    Mammalia Nqo21 , 5 NAD(P)H dehydrogenase, quinone 21, 5 82.68(n)1
    81.66(a)1
      13 (14.01 cM)5
    181051  NM_001163241.11  NP_001156713.11 
     339646595 
    chicken
    (Gallus gallus)
    Aves NQO21 NAD(P)H dehydrogenase, quinone 2 71.62(n)
    71.18(a)
      420886  XM_418973.3  XP_418973.1 
    lizard
    (Anolis carolinensis)
    Reptilia NQO26
    --
    62(a)
    1 ↔ 1
    GL343247.1(945747-950320)
    zebrafish
    (Danio rerio)
    Actinopterygii nqo16
    NAD(P)H dehydrogenase, quinone 1
    41(a)
    1 ↔ 1
    7(57966520-57985583)
    honey bee
    (Apis mellifera)
    Insecta --
    --
    24(a)
    possible ortholog
    GroupUn.6733(491-1051)
    E. coli
    (Escherichia coli)
    Gamma proteobacteria kefG6
    kefF6
    (see all 3)
    potassium-efflux system ancillary protein for KefB...
    potassium-efflux system ancillary protein for KefC...
    (see all 3)
    33(a)
    32(a)
    (see all 3)
    possible ortholog
    possible ortholog
    (see all 3)
    Chromosome(3478629-3479183)
    Chromosome(47246-47776)


    ENSEMBL Gene Tree for NQO2 (if available)
    TreeFam Gene Tree for NQO2 (if available) 

    (Paralogs according to 1HomoloGene,
    2Ensembl, and 3SIMAP, Pseudogenes according to 4Pseudogene.org Build 68)
    About This Section
    Paralogs for NQO2 gene
    NQO12  
    1 SIMAP similar gene for NQO2 using alignment to 4 protein entries:     NQO2_HUMAN (see all proteins):
    NQO1

    NQO2 for paralogs           About GeneDecksing


    1 Pseudogenes.org Pseudogene for NQO2
    PGOHUM00000243468


    (SNPs/Variants according to the 1NCBI SNP Database, 2Ensembl, 3PupaSUITE, UniProtKB, and DNA2.0, Linkage Disequilibrium by HapMap, Structural Variations(CNVs/InDels/Inversions) from the Database of Genomic Variants, Mutations from the Human Gene Mutation Database (HGMD) and the Locus Specific Mutation Databases (LSDB), Blood group antigen gene mutations by BGMUT, Resequencing Primers from QIAGEN, Cancer Mutation PCR Arrays and Assays and Copy Number PCR Arrays from SABiosciences)
    About This Section

    10/585 NCBI SNPs in NQO2 are shown (see all 585    About this table
    Genomic DataTranscription Related DataAllele Frequencies
    SNP IDValidClinical
    significance
    Chr 6 posSequence#AA
    Chg
    TypeMore#Allele
    freq
    PopTotal
    sample
    More
    ----------
    rs77467241,2
    C,F,--2998075(+) CTTTAT/CGTTAT 1 -- us2k15Minor allele frequency- C:0.18WA CSA NA 244
    rs1119739551,2
    C,--2998116(+) GATGCT/GGGTAG 1 -- us2k12Minor allele frequency- G:0.06WA 120
    rs77601371,2
    C,F,A,H,--2998124(+) TAGCAG/CAAGGG 1 -- us2k1 trp311Minor allele frequency- C:0.46NA WA CSA EA 374
    rs77428131,2
    C,F,A,H,--2998164(+) CAATGA/TCCTCT 1 -- us2k111Minor allele frequency- T:0.40NA WA CSA EA 374
    rs77603271,2
    C,--2998248(+) GGGGCG/TTTGGG 1 -- us2k10--------
    rs65969271,2
    C,F,A,H,--2998319(+) CTTGCA/TTTCCA 1 -- us2k14Minor allele frequency- T:0.38WA NA 8
    rs65969281,2
    C,F,A,H,--2998349(+) GAAAAG/TTGAGA 1 -- us2k15Minor allele frequency- T:0.13NA WA 244
    rs1403879341,2
    --2998384(+) TTTGTC/TGTTGG 1 -- us2k10--------
    rs1142094581,2
    F,--2998416(+) GTAGCA/GTGACC 1 -- us2k11Minor allele frequency- G:0.03NA 120
    rs1448298241,2
    --2998452(+) ATGGTC/TAATCT 1 -- us2k10--------

    HapMap Linkage Disequilibrium report for NQO2 (2988221 - 3019996 bp)
    Structural Variations (Copy Number Variations, Insertions/Deletions, Inversions)
    Database of Genomic Variants (DGV): 1 variation for NQO2
         1 CNV: 2617
    Human Gene Mutation Database (HGMD): NQO2

    SABiosciences Cancer Mutation PCR Assays
    QIAGEN SeqTarget long-range PCR primers in human, mouse, rat for resequencing NQO2
    DNA2.0 Custom Variant and Variant Library Synthesis for NQO2

    (in which this Gene is Involved, According to MalaCards, OMIM, UniProtKB, the University of Copenhagen DISEASES database, Novoseek, Genatlas, GeneTests, GAD, HuGE Navigator, and/or TGDB.)
    About This Section

    NQO2 for disorders           About GeneDecksing

    OMIM gene information: 160998   
    OMIM disorders: 114480  
    20/22 diseases for NQO2 (see all 22):    About MalaCards
    substance dependence    breast cancer susceptibility    acute myeloid leukemia    herpes simplex
    myeloid leukemia    hepatoblastoma    parkinson's disease    alcoholic pancreatitis
    rubella    myelodysplastic syndrome    breast cancer    schizophrenia
    alcoholism    pancreatitis    ovarian cancer    gastric cancer
    influenza    pancreatic cancer    leukemia    melanoma

    7 Novoseek disease relationships for NQO2 gene    About this table

    Disease   -log (P-Val)   Hits   PubMed IDs for Articles with Shared Sentences (# sentences)
    hepatoblastoma 48.9 4 1691923 (1), 8182056 (1)
    agranulocytosis 32.1 1 14617031 (1)
    parkinson disease 30 6 18314446 (2), 11688992 (1), 15451063 (1), 18579530 (1) (see all 5)
    cancer 13 6 10945627 (1), 16129418 (1), 17643990 (1), 18062662 (1)
    melanoma 9.46 2 15993843 (2)
    schizophrenia 8.78 6 14639047 (4), 16955993 (1)
    tumors 0.903 7 18794327 (3), 14529407 (2), 11809856 (1), 16955993 (1)

    Genetic Association Database (GAD): NQO2
    Human Genome Epidemiology (HuGE) Navigator: NQO2 (20 documents)

    Export disorders for NQO2 gene to outside databases

    (in PubMed. Associations of this gene to articles via 1Entrez Gene, 2UniProtKB/Swiss-Prot, 3HGNC, 4GAD, 5PharmGKB, 6HMDB, 7DrugBank, 8UniProtKB/TrEMBL, 9 Novoseek, and/or 10fRNAdb)
    About This Section

    PubMed articles for NQO2 gene, integrated from 9 sources (see all 116):
    (articles sorted by number of sources associating them with NQO2)
        Utopia: connect your pdf to the dynamic
    world of online information

    1. Crystal structure of quinone reductase 2 in complex with resveratrol. (PubMed id 15350128)1, 2, 7, 9 Buryanovskyy L....Zhang Z. (2004)
    2. Nucleotide and deduced amino acid sequence of a human cDNA (NQO2) corresponding to a second member of the NAD(P)H:quinone oxidoreductase gene family. Extensive polymorphism at the NQO2 gene locus on chromosome 6. (PubMed id 1691923)1, 2, 3, 9 Jaiswal A.K.... McBride O.W. (1990)
    3. Kinetic mechanism of quinone oxidoreductase 2 and its inhibition by the antimalarial quinolines. (PubMed id 15078100)1, 2, 7, 9 Kwiek J.J.... Rudolph J. (2004)
    4. Crystal structure of human quinone reductase type 2, a metalloflavoprotein. (PubMed id 10433694)1, 2, 7, 9 Foster C.E.... Amzel L.M. (1999)
    5. Catalytic properties of NAD(P)H:quinone oxidoreductase-2 (NQO2), a dihydronicotinamide riboside dependent oxidoreductase. (PubMed id 9367528)1, 2, 9 Wu K.... Chen S. (1997)
    6. Kinetic, thermodynamic and X-ray structural insights into the interaction of melatonin and analogues with quinone reductase 2. (PubMed id 18254726)1, 2, 9 Calamini B.... Mesecar A.D. (2008)
    7. Human NAD(P)H:quinone oxidoreductase 2. Gene structure, activity, and tissue-specific expression. (PubMed id 8182056)1, 2, 9 Jaiswal A.K. (1994)
    8. Quinone reductase 2 is a catechol quinone reductase. (PubMed id 18579530)1, 2, 9 Fu Y.... Zhang Z. (2008)
    9. A possible association between an insertion/deletion polymorphism of the NQO2 gene and schizophrenia. (PubMed id 14639047)1, 4, 9 Harada S....Kawanishi Y. (2003)
    10. Association analyses between polymorphisms of the phase II detoxification enzymes (GSTM1, NQO1, NQO2) and alcohol withdrawal symptoms. (PubMed id 12960511)1, 4, 9 Okubo T....Matsushita S. (2003)

    (in PubMed, OMIM, and NCBI Bookshelf)
    About This Section
     ANDOR
    Aliases
    Disorders
    Free Text  

      Query String
    PubMed
    OMIM
    NCBI Bookshelf
      (Note: In FireFox, select the above section and copy using Ctrl-C)

    (According to Entrez Gene, HGNC, AceView, euGenes, Ensembl, miRBase, ECgene, Kegg, and/or H-InvDB)
    About This Section
    Entrez Gene: 4835 HGNC: 7856 AceView: NQO2andDKFZp686I15217 Ensembl:ENSG00000124588 euGenes: HUgn4835
    ECgene: NQO2 H-InvDB: NQO2

    (According to HUGE)
    About This Section
      --

    (According to PharmGKB, ATLAS, HORDE, IMGT, LEIDEN, UniProtKB/Swiss-Prot, and/or UniProtKB/TrEMBL,
    Wikipedia and/or GeneReviews via UniProtKB/Swiss-Prot)
    About This Section
    NameDescription
    PharmGKB entry for NQO2 Pharmacogenomics, SNPs, Pathways
    NIEHS-SNPshttp://egp.gs.washington.edu/data/nqo2/

    (Patent information from GeneIP,
    Licensable technologies from WIS Yeda, Salk, Tufts,
    IP news from LifeMap Sciences, Inc.)
    About This Section
    Patent Information for NQO2 gene:
    Search GeneIP for patents involving NQO2

    GeneCards and IP:
    Japan Patent Office Licenses GeneCards     European Patent Office Licenses GeneCards     Improving the IP Search



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