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NOL4 Gene

protein-coding   GIFtS: 54
GCID: GC18M031465

Nucleolar Protein 4

  Search for NOL4
at  

(According to 1HGNC, 2Entrez Gene,
3UniProtKB/Swiss-Prot, 4UniProtKB/TrEMBL, 5OMIM, 6GeneLoc, 7Ensembl, 8DME, 9miRBase, 10fRNAdb, 12H-InvDB, 13NCBI, 14NONCODE, and/or 15RNAdb)
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Aliases
Nucleolar Protein 41 2
Cancer/Testis Antigen 1251 2
NOLP2 3
CT1252
Nucleolar Localized Protein2
Nucleolar-Localized Protein3

External Ids:    HGNC: 78701   Entrez Gene: 87152   Ensembl: ENSG000001017467   OMIM: 6035775   UniProtKB: O948183   

Export aliases for NOL4 gene to outside databases

Previous GC identifers: GC18M031251 GC18M029684 GC18M029686 GC18M028290


(According to Entrez Gene, GeneCards, Tocris Bioscience, Wikipedia's Gene Wiki, PharmGKB,
UniProtKB/Swiss-Prot, and/or UniProtKB/TrEMBL)
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GeneCards Summary for NOL4 Gene:
NOL4 (nucleolar protein 4) is a protein-coding gene. GO annotations related to this gene include RNA binding. An important paralog of this gene is C20orf112.

Gene Wiki entry for NOL4 Gene


(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 75), Regulatory elements and Epigenetics data according to QIAGEN, and/or SwitchGear Genomics)
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RefSeq DNA sequence at NCBI GenBank:
NC_000018.9  NT_010966.15  NC_018929.2  
Regulatory elements:
   Regulatory transcription factor binding sites in the NOL4 gene promoter:
         Max1   Nkx2-5   MIF-1   POU6F1 (c2)   S8   HSF2   Meis-1a   Pax-4a   c-Myc   Meis-1   
         Other transcription factors

SwitchGear Promoter luciferase reporter plasmidNOL4 promoter sequence
   Search Chromatin IP Primers for NOL4

Epigenetics:
DNA Methylation CpG Assay Predesigned for Pyrosequencing in human, mouse, rat NOL4


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

Entrez Gene cytogenetic band: 18q12   Ensembl cytogenetic band:  18q12.1   HGNC cytogenetic band: 18q12

NOL4 Gene in genomic location: bands according to Ensembl, locations according to (and/or Entrez Gene and/or Ensembl if different)
NOL4 gene location

GeneLoc information about chromosome 18         GeneLoc Exon Structure

GeneLoc location for GC18M031465:  view genomic region     (about GC identifiers)

Start:
31,431,064 bp from pter      End:
31,804,916 bp from pter
Size:
373,853 bases      Orientation:
minus strand

(According to 1UniProtKB, HORDE, 2neXtProt, Ensembl, and/or Reactome, Modification sites according to PhosphoSitePlus, Specific Peptides from DME, 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, Cloud-Clone Corp., and/or eBioscience,
Biochemical Assays by EMD Millipore, R&D Systems, OriGene, GenScript, Cell Signaling Technology, Enzo Life Sciences, Cloud-Clone Corp., and/or eBioscience, Antibodies by EMD Millipore, R&D Systems, Cell Signaling Technology, OriGene, Novus Biologicals, Thermo Fisher Scientific, LSBio, Abcam, Cloud-Clone Corp, and/or others.)
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UniProtKB/Swiss-Prot: NOL4_HUMAN, O94818 (See protein sequence)
Recommended Name: Nucleolar protein 4  
Size: 638 amino acids; 71357 Da
Sequence caution: Sequence=AAH00313.1; Type=Miscellaneous discrepancy; Note=Contaminating sequence. Sequence of
unknown origin in the N-terminal part; Sequence=BAA34576.1; Type=Erroneous termination; Positions=38;
Note=Translated as Gln; Sequence=BAA34576.1; Type=Frameshift; Positions=82;
Secondary accessions: B4DSQ0 B7Z3Z7 F5H1E3 Q6IBS2 Q9BWF1
Alternative splicing: 4 isoforms:  O94818-1   O94818-2   O94818-3   O94818-4   (No experimental confirmation available)

Explore the universe of human proteins at neXtProt for NOL4: NX_O94818

Explore proteomics data for NOL4 at MOPED

Post-translational modifications: 

  • Modification sites at neXtProt
  • Modification sites at PhosphoSitePlus

  • See NOL4 Protein Expression from SPIRE MOPED, PaxDB, and MaxQB

    REFSEQ proteins (6 alternative transcripts): 
    NP_001185475.1  NP_001185476.1  NP_001185477.1  NP_001185478.1  NP_001269456.1  NP_003778.2  

    ENSEMBL proteins: 
     ENSP00000261592   ENSP00000445733   ENSP00000464704   ENSP00000465450   ENSP00000443472  
     ENSP00000467629   ENSP00000467015   ENSP00000467326   ENSP00000464790   ENSP00000269185  
     ENSP00000438190  

    NOL4 Human Recombinant Protein Products:

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    (According to HGNC, IUPHAR, InterPro, ProtoNet, UniProtKB, and/or BLOCKS, Sets of similar genes according to GeneDecks)
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    1 InterPro protein domain:
     IPR026747 NOL4

    Graphical View of Domain Structure for InterPro Entry O94818

    ProtoNet protein and cluster: O94818


    Find genes that share domains with NOL4           About GenesLikeMe


    (According to 1UniProtKB, Genatlas, LifeMap Discovery™, IUBMB, and/or 2DME, Human phenotypes from GenomeRNAi, Animal models from MGI Mar 06 2013, inGenious Targeting Laboratory, genOway,
    transcription factor targeting from QIAGEN and/or HOMER, miRNA Gene Targets from miRTarBase, shRNA from OriGene, siRNAs from OriGene, QIAGEN, microRNA from QIAGEN, SwitchGear Genomics, Gene Editing from DNA2.0, Clones from OriGene, GenScript, Sino Biological, DNA2.0, Vector BioLabs and/or Addgene, Cell Lines from GenScript, ESI BIO, In Situ Hybridization Assays from Advanced Cell Diagnostics, Flow cytometry from eBioscience, Ontologies according to Gene Ontology Consortium 01 Apr 2014 via Entrez Gene.)
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    Molecular Function:
         Genatlas biochemistry entry for NOL4:
    nucleolar protein 4

         Gene Ontology (GO): 1 molecular function term:    About this table

    GO IDQualified GO termEvidencePubMed IDs
    GO:0003723RNA binding TAS9813152
         
    Find genes that share ontologies with NOL4           About GenesLikeMe


    Phenotypes:
         1 GenomeRNAi human phenotype for NOL4:
     Synthetic lethal with Ras 

    Animal Models:
       inGenious Targeting Laboratory: Let us create your new Knockout/Knockin mouse model for NOL4
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       genOway customized KO model: permanent, tissue-specific or time-controlled inactivation for NOL4
       genOway customized Knockin model: humanization, point mutation, expression monitoring, etc. for NOL4

    miRNA
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    miRTarBase miRNAs that target NOL4:
    hsa-mir-335-5p (MIRT016812), hsa-mir-181a-5p (MIRT025082)

    Block miRNA regulation of human, mouse, rat NOL4 using miScript Target Protectors
    Selected qRT-PCR Assays for microRNAs that regulate NOL4 (see all 81):
    hsa-miR-411* hsa-miR-323-3p hsa-miR-548j hsa-miR-106a hsa-miR-128 hsa-miR-219-5p hsa-miR-519a hsa-miR-10b*
    SwitchGear 3'UTR luciferase reporter plasmidNOL4 3' UTR sequence
    Inhib. RNA
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    Predesigned siRNA for gene silencing in human, mouse, rat NOL4

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    In Situ Assay
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    Advanced Cell Diagnostics RNAscope RNA in situ hybridization assays for NOL4


    (According to UniProtKB, COMPARTMENTS Subcellular localization database, Ontologies according to Gene Ontology Consortium 01 Apr 2014 via Entrez Gene.)
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    Subcellular locations from UniProtKB/Swiss-Prot
    NOL4_HUMAN, O94818: Nucleus, nucleolus
    Subcellular locations from COMPARTMENTS: 

    CompartmentConfidence
    nucleus5

    Gene Ontology (GO): 1 cellular component term:    About this table

    GO IDQualified GO termEvidencePubMed IDs
    GO:0005730nucleolus IEA--

    Find genes that share ontologies with NOL4           About GenesLikeMe


    (SuperPaths according to PathCards, Pathways according to R&D Systems, Cell Signaling Technology, KEGG, PharmGKB, BioSystems, Sino Biological, Reactome, Tocris Bioscience, GeneGo (Thomson Reuters), QIAGEN, and/or UniProtKB, Sets of similar genes according to GeneDecks, Interaction Networks according to QIAGEN, 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 Apr 2014 via Entrez Gene).
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        Custom Pathway & Disease-focused RT2 Profiler PCR Arrays for NOL4
    Interactions:

        Search GeneGlobe Interaction Network for NOL4

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

    Selected Interacting proteins for NOL4 (O948182, 3 ENSP000002615924) via UniProtKB, MINT, STRING, and/or I2D (see all 9)
    InteractantInteraction Details
    GeneCardExternal ID(s)
    SNAPC5O759712, 3, ENSP000003195974MINT-68388 I2D: score=5 STRING: ENSP00000319597
    PRMT1Q998732, 3MINT-63240 I2D: score=4 
    MAPK6Q166592, 3MINT-8261549 I2D: score=2 
    MAGEA11P433642, 3, ENSP000003473584MINT-66423 I2D: score=5 STRING: ENSP00000347358
    CTBP2P565453, ENSP000003118254I2D: score=4 STRING: ENSP00000311825
    About this table

    (Chemical Compounds according to UniProtKB, Enzo Life Sciences, EMD Millipore, Tocris Bioscience, ApexBio, HMDB, BitterDB, and/or Novoseek, Ligands according to IUPHAR, and Drugs according to DrugBank, Enzo Life Sciences, and/or PharmGKB)
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    Browse Small Molecules at EMD Millipore
       Browse drugs & compounds from Enzo Life Sciences
      Browse compounds at ApexBio 

    Browse Tocris compounds for NOL4



    (Secondary structures according to fRNAdb,
    GenBank/EMBL/DDBJ Accessions according to
    Unigene (Build 236 Homo sapiens; Apr 25 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,
    siRNAs from OriGene, QIAGEN, shRNA from OriGene, microRNA from QIAGEN, SwitchGear Genomics,
    Tagged/untagged cDNA clones from OriGene, GenScript, DNA2.0, Vector BioLabs, and/or Addgene, Primers from OriGene, and/or QIAGEN, Flow cytometry from eBioscience )
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    REFSEQ mRNAs for NOL4 gene (6 alternative transcripts): 
    NM_001198546.1  NM_001198547.1  NM_001198548.1  NM_001198549.1  NM_001282527.1  NM_003787.4  

    Unigene Cluster for NOL4:

    Nucleolar protein 4
    Hs.514795  [show with all ESTs]
    Unigene Representative Sequence: NM_003787
    16 Ensembl transcripts including schematic representations, and UCSC links where relevant:
    ENST00000261592(uc010xbs.2 uc002kxr.4 uc010xbt.2 uc010dmh.3 uc010dmi.3 uc010xbu.2)
    ENST00000535384(uc010xbv.1) ENST00000586314 ENST00000589544 ENST00000538587
    ENST00000590712 ENST00000586553 ENST00000588280 ENST00000591917 ENST00000587971
    ENST00000587953 ENST00000586309 ENST00000590846 ENST00000588355 ENST00000269185(uc002kxt.4)
    ENST00000535475
    miRNA
    Products:
         
    Block miRNA regulation of human, mouse, rat NOL4 using miScript Target Protectors
    Selected qRT-PCR Assays for microRNAs that regulate NOL4 (see all 81):
    hsa-miR-411* hsa-miR-323-3p hsa-miR-548j hsa-miR-106a hsa-miR-128 hsa-miR-219-5p hsa-miR-519a hsa-miR-10b*
    SwitchGear 3'UTR luciferase reporter plasmidNOL4 3' UTR sequence
    Inhib. RNA
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    GenScript: all cDNA clones in your preferred vector (see all 5): NOL4 (NM_001198547)
    DNA2.0 Custom Codon Optimized Gene Synthesis Service for NOL4
    Vector BioLabs ready-to-use adenovirus/AAV for human, mouse, rat NOL4
    Primer
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    OriGene qPCR primer pairs and template standards for NOL4
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    Pre-validated RT2 qPCR Primer Assay in human, mouse, rat NOL4
      QuantiTect SYBR Green Assays in human, mouse, rat NOL4
      QuantiFast Probe-based Assays in human, mouse, rat NOL4

    Additional mRNA sequence: 

    AB015339.1 AB017800.1 AK091463.1 AK296539.1 AK297185.1 AK299850.1 AK312562.1 BC000313.2 
    BT006763.1 CR456730.1 NR_036752.1 

    9 DOTS entries:

    DT.412647  DT.121090082  DT.100708122  DT.91712623  DT.100746870  DT.121084267  DT.40127323  DT.91712622 
    DT.100746869 

    Selected AceView cDNA sequences (see all 89):

    H09988 AW248833 CR608782 BI755747 BI830078 AA430033 AI243344 BM973283 
    BP370892 AK091463 BF219730 BX424616 BE791757 AV704251 T16121 BM312832 
    CA865772 BM505405 BP369540 BX281610 BE793687 CA865522 BE252468 AI468245 

    GeneLoc Exon Structure

    3 Alternative Splicing Database (ASD) splice patterns (SP) for NOL4    About this scheme

    ExUns: 1a · 1b ^ 2 ^ 3 ^ 4 ^ 5 ^ 6 ^ 7 ^ 8 ^ 9 ^ 10 ^ 11 ^ 12 ^ 13
    SP1:              -           -                                                         
    SP2:                                                              -                     
    SP3:              -           -                                   -     -               


    ECgene alternative splicing isoforms for NOL4

    (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™, Protein expression images according to data from SPIRE 1MOPED, 2PaxDb, and 3MaxQB, plus additional links to SOURCE, and/or BioGPS, and/or UniProtKB,
    PCR Arrays from QIAGEN, Primers from OriGene, and/or QIAGEN, In Situ Hybridization Assays from Advanced Cell Diagnostics)
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    NOL4 expression in normal human tissues (normalized intensities)
    See probesets specificity/sensitivity at GeneAnnot
    About this imageBioGPS <intensity>2/3
    CGAP TAG: TAAAATTTAT
    NOL4 Expression
    About this image


    NOL4 expression in embryonic tissues and stem cells    About this table
    Data from LifeMap, the Embryonic Development and Stem Cells Database
     selected tissues (see all 6) fully expand
     
     Eye (Sensory Organs)    fully expand to see all 2 entries
             Glycinergic Amacrine Cells Inner Nuclear Layer
             Retina
     
     Pancreas (Endocrine System)    fully expand to see all 2 entries
             Endocrine Progenitor Cells Ventral Pancreatic Bud
     
     Neurons
             Glycinergic Amacrine Cells Inner Nuclear Layer
     
     Testis (Reproductive System)
     
     Spinal Cord (Nervous System)
    NOL4 Protein expression data from MOPED1, PaxDb2 and MaxQB3    About this image

    NOL4 Protein Expression

    SOURCE GeneReport for Unigene cluster: Hs.514795

    UniProtKB/Swiss-Prot: NOL4_HUMAN, O94818
    Tissue specificity: Expressed predominantly in fetal brain, adult brain and testis

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    In Situ
    Assay Products:
     

     
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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)
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    This gene was present in the common ancestor of animals.

    Orthologs for NOL4 gene from Selected species (see all 11)    About this table
    Organism Taxonomic
    classification
    Gene Description Human
    Similarity
    Orthology
    Type
    Details
    mouse
    (Mus musculus)
    Mammalia Nol41 , 5 nucleolar protein 41, 5 89.68(n)1
    93.81(a)1
      18 (11.96 cM)5
    3192111  NM_001161483.11  NP_001154955.11 
     226931815 
    chicken
    (Gallus gallus)
    Aves NOL41 nucleolar protein 4 88.3(n)
    93.64(a)
      769466  XM_001232141.3  XP_001232142.2 
    lizard
    (Anolis carolinensis)
    Reptilia NOL46
    nucleolar protein 4
    87(a)
    1 ↔ 1
    GL343207.1(2437151-2583695)
    tropical clawed frog
    (Xenopus tropicalis)
    Amphibia nol41 nucleolar protein 4 80.75(n)
    85.47(a)
      100494971  XM_002934128.2  XP_002934174.2 
    fruit fly
    (Drosophila melanogaster)
    Insecta BG:DS01523.13   -- 75(a)   35A1   --


    ENSEMBL Gene Tree for NOL4 (if available)
    TreeFam Gene Tree for NOL4 (if available)

    (Paralogs according to 1HomoloGene,
    2Ensembl, and 3SIMAP, Pseudogenes according to 4Pseudogene.org Build 68)
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    Paralogs for NOL4 gene
    C20orf1122  
    2 SIMAP similar genes for NOL4 using alignment to 7 protein entries:     NOL4_HUMAN (see all proteins):
    C20orf112    LOC284804

    Find genes that share paralogs with NOL4           About GenesLikeMe



    (SNPs/Variants according to the 1NCBI SNP Database, 2Ensembl, 3PupaSUITE, 4UniProtKB, 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), the Human Cytochrome P450 Allele Nomenclature Database, and the Locus Specific Mutation Databases (LSDB), Blood group antigen gene mutations by BGMUT, Resequencing Primers, Cancer Mutation PCR Arrays and Assays, and Copy Number PCR Arrays from QIAGEN)
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    Selected SNPs for NOL4 (see all 6233)    About this table                                 

    Genomic DataTranscription Related DataAllele Frequencies
    SNP IDValidClinical
    significance
    Chr 18 posSequence#AA
    Chg
    TypeMore#Allele
    freq
    PopTotal
    sample
    More
    ----------
    rs28527451,2
    H--31430695(+) AAGGCA/CAAGTA 6 -- int14Minor allele frequency- C:0.00NS EA 394
    rs752718111,2
    F--31430714(+) GCACTT/CAAAAC 6 -- int11Minor allele frequency- C:0.01NA 120
    rs1814406031,2
    --31430772(+) AACAGA/GTTACT 6 -- int10--------
    rs1858770011,2
    --31430928(+) CTTAGA/GATATT 6 -- int10--------
    rs1147404491,2
    F--31430972(+) CTAAAC/TGTAGG 6 -- int11Minor allele frequency- T:0.02WA 118
    rs1912593741,2
    --31431371(+) TTACTC/TGGTCA 6 -- ut31 nc-transcript-variant0--------
    rs1814293941,2
    --31431402(+) AAAACC/TATATG 6 -- ut31 nc-transcript-variant0--------
    rs1860657901,2
    --31431466(+) AATGAC/TATAAA 6 -- ut31 nc-transcript-variant0--------
    rs1908831981,2
    --31431472(+) ATAAAC/TTTTAC 6 -- ut31 nc-transcript-variant0--------
    rs10459541,2
    C,F,H--31431529(-) TTTAGC/ATTTGG 6 -- nc-transcript-variantut3117Minor allele frequency- A:0.11MN NS EA NA WA 2142

    HapMap Linkage Disequilibrium report for NOL4 (31431064 - 31681064 bp, first 250kb of NOL4)

    Structural Variations
         Database of Genomic Variants (DGV) Selected variations for NOL4 (see all 20):    About this table    
    Variant IDTypeSubtypePubMed ID
    esv3222CNV Deletion18987735
    esv2019786CNV Deletion18987734
    esv2716952CNV Deletion23290073
    esv1694854CNV Deletion17803354
    esv2670669CNV Deletion23128226
    esv2663858CNV Deletion23128226
    esv1010069CNV Deletion20482838
    esv2668525CNV Deletion23128226
    esv267479CNV Insertion20981092
    nsv132109CNV Insertion16902084

    Site Specific Mutation Identification with PCR Assays
    SeqTarget long-range PCR primers for resequencing NOL4
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    (in which this Gene is Involved, According to MalaCards, OMIM, UniProtKB, the University of Copenhagen DISEASES database, Genatlas, GeneTests, GAD, HuGE Navigator, and/or TGDB.)
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    OMIM gene information: 603577    OMIM disorders: --


    Find genes that share disorders with NOL4           About GenesLikeMe

    Genetic Association Database (GAD): NOL4
    Human Genome Epidemiology (HuGE) Navigator: NOL4 (1 document)

    Export disorders for NOL4 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)
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    PubMed articles for NOL4 gene, integrated from 10 sources (see all 18):
    (articles sorted by number of sources associating them with NOL4)
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    1. NOLP: identification of a novel human nucleolar protein and determination of sequence requirements for its nucleolar localization. (PubMed id 9813152)1, 2, 3 Ueki N....Muramatsu M.-A. (Biochem. Biophys. Res. Commun. 1998)
    2. Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score. (PubMed id 20379614)1, 4 Rose J.E....Uhl G.R. (Mol. Med. 2010)
    3. A genomewide association study of citalopram response in major depressive disorder. (PubMed id 19846067)1, 4 Garriock H.A....Hamilton S.P. (Biol. Psychiatry 2010)
    4. The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC). (PubMed id 15489334)1, 2 Gerhard D.S.... Malek J. (Genome Res. 2004)
    5. Complete sequencing and characterization of 21,243 full-length human cDNAs. (PubMed id 14702039)1, 2 Ota T.... Sugano S. (Nat. Genet. 2004)
    6. Selection system for genes encoding nuclear-targeted proteins. (PubMed id 9853615)1, 2 Ueki N.... Muramatsu M.-A. (Nat. Biotechnol. 1998)
    7. Genetic variants associated with breast size also influence breast cancer risk. (PubMed id 22747683)1 Eriksson N....Tung J.Y. (BMC Med. Genet. 2012)
    8. A directed protein interaction network for investigating intracellular signal transduction. (PubMed id 21900206)1 Vinayagam A....Wanker E.E. (Sci Signal 2011)
    9. Genome-wide association to body mass index and waist circumference: the Framingham Heart Study 100K project. (PubMed id 17903300)4 Fox C.S....Atwood L.D. (BMC Med. Genet. 2007)
    10. Genome-wide association of echocardiographic dimensions, brachial artery endothelial function and treadmill exercise responses in the Framingham Heart Study. (PubMed id 17903301)4 Vasan R.S....Benjamin E.J. (BMC Med. Genet. 2007)

    (in PubMed, OMIM, and NCBI Bookshelf)
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    (According to Entrez Gene, HGNC, AceView, euGenes, Ensembl, miRBase, ECgene, Kegg, and/or H-InvDB)
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    Entrez Gene: 8715 HGNC: 7870 AceView: NOL4 Ensembl:ENSG00000101746 euGenes: HUgn8715
    ECgene: NOL4 H-InvDB: NOL4

    (According to HUGE)
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    (According to PharmGKB, ATLAS, HORDE, IMGT, LEIDEN, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL, and/or others, e.g. Wikipedia and GeneReviews, via UniProtKB/Swiss-Prot)
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    NameDescription
    PharmGKB entry for NOL4 Pharmacogenomics, SNPs, Pathways

    (Patent information from GeneIP,
    Licensable technologies from WIS Yeda, Salk, Tufts,
    IP news from LifeMap Sciences, Inc.)
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    Patent Information for NOL4 gene:
    Search GeneIP for patents involving NOL4

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



    (Antibodies, recombinant proteins, and assays from EMD Millipore, R&D Systems, OriGene, QIAGEN, GenScript, Cell Signaling Technology, Novus Biologicals, Sino Biological, Enzo Life Sciences, Abcam, ProSpec, Cloud-Clone Corp., Thermo Fisher Scientific, LSBio, eBioscience, and/or others, Gene Editing from DNA2.0. Clones from OriGene, GenScript, Sino Biological, DNA2.0, SwitchGear Genomics, Vector BioLabs, Addgene, Cell lines from GenScript, and ESI BIO, Flow cytometery from eBioscience, PCR Arrays from QIAGEN, Drugs and/or compounds from EMD Millipore, Tocris Bioscience, Enzo Life Sciences, and/or ApexBio, In Situ Hybridization Assays from
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