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

NRAS Gene

protein-coding   GIFtS: 70
GCID: GC01M115247

neuroblastoma RAS viral (v-ras) oncogene homolog

 Explore 80 diseases affiliated with
NRAS via our new
 Human Malady Compendium 
Biological research products
for NRAS
    

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

Aliases
Neuroblastoma RAS Viral (V-Ras) Oncogene Homolog1 2     NRAS12
N-Ras1     GTPase NRas2
Transforming Protein N-Ras2 3     N-Ras Protein Part 42
ALPS42 5     V-Ras Neuroblastoma RAS Viral Oncogene Homolog2
NS62 5     HRAS13

External Ids:    HGNC: 79891   Entrez Gene: 48932   Ensembl: ENSG000002132817   OMIM: 1647905   UniProtKB: P011113   

Export aliases for NRAS gene to outside databases

Previous GC identifers: GC01M115662 GC01M114131 GC01M114349 GC01M114548 GC01M114961 GC01M115048 GC01M113105


(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 NRAS:
This is an N-ras oncogene encoding a membrane protein that shuttles between the Golgi apparatus and the plasma
membrane. This shuttling is regulated through palmitoylation and depalmitoylation by the ZDHHC9-GOLGA7 complex. The
encoded protein, which has intrinsic GTPase activity, is activated by a guanine nucleotide-exchange factor and
inactivated by a GTPase activating protein. Mutations in this gene have been associated with somatic rectal cancer,
follicular thyroid cancer, autoimmune lymphoproliferative syndrome, Noonan syndrome, and juvenile myelomonocytic
leukemia. (provided by RefSeq, Jun 2011)

UniProtKB/Swiss-Prot: RASN_HUMAN, P01111
Function: Ras proteins bind GDP/GTP and possess intrinsic GTPase activity

Gene Wiki entry for NRAS (Neuroblastoma RAS viral oncogene homolog)


(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_000001.10  NC_018912.1  NT_032977.9  
Regulatory elements:
   SABiosciences Regulatory transcription factor binding sites in the NRAS gene promoter:
         c-Fos   AP-1   ATF-2   STAT3   MyoD   c-Jun   
         Other transcription factors

SwitchGear Promoter luciferase reporter plasmidNRAS promoter sequence
   Search SABiosciences Chromatin IP Primers for NRAS

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


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

Entrez Gene cytogenetic band: 1p13.2   Ensembl cytogenetic band:  1p13.2   HGNC cytogenetic band: 1p13.2

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

GeneLoc information about chromosome 1         GeneLoc Exon Structure

GeneLoc location for GC01M115247:  view genomic region     (about GC identifiers)

Start:
115,247,078 bp from pter      End:
115,259,515 bp from pter
Size:
12,438 bases      Orientation:
minus 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: RASN_HUMAN, P01111 (See protein sequence)
Recommended Name: GTPase NRas precursor  
Size: 189 amino acids; 21229 Da
Subunit: Interacts (active GTP-bound form preferentially) with RGS14 (By similarity). Interacts (active GTP-bound form)
with RASSF7
Subcellular location: Cell membrane; Lipid-anchor; Cytoplasmic side. Golgi apparatus membrane; Lipid-anchor.
Note=Shuttles between the plasma membrane and the Golgi apparatus
Miscellaneous: Mutations which change AA 12, 13 or 61 activate the potential of Ras to transform cultured cells and are
implicated in a variety of human tumors
1 PDB 3D structure from and Proteopedia for NRAS:
3CON (3D)    
Secondary accessions: Q14971 Q15104 Q15282

Explore the universe of human proteins at neXtProt for NRAS: NX_P01111

Post-translational modifications:

  • Palmitoylated by the ZDHHC9-GOLGA7 complex. A continuous cycle of de- and re-palmitoylation regulates rapid exchange
  • between plasma membrane and Golgi1
  • Acetylation at Lys-104 prevents interaction with guanine nucleotide exchange factors (GEFs) (By similarity)1
  • View modification sites using PhosphoSitePlus2
  • View neXtProt modification sites for NX_P01111

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

    REFSEQ proteins: NP_002515.1  
    ENSEMBL proteins: 
     ENSP00000358548  
    Reactome Protein details: P01111
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    Uscn Proteins for NRAS

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

    GO IDQualified GO termEvidencePubMed IDs
    GO:0000139Golgi membrane IEA--
    GO:0005624membrane fraction ----
    GO:0005886plasma membrane TAS--


    NRAS for ontologies           About GeneDecksing



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    Uscn ELISAs and CLIAs for NRAS


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

    NRAS for domains           About GeneDecksing

    3 InterPro domains/families:
     IPR005225 Small_GTP-bd_dom
     IPR001806 Small_GTPase
     IPR020849 Small_GTPase_Ras

    Graphical View of Domain Structure for InterPro Entry P01111

    ProtoNet protein and cluster: P01111

    2 Blocks protein families:
    IPB001806 Transforming protein P21 RAS signature
    IPB003577 Ras small GTPase


    UniProtKB/Swiss-Prot: RASN_HUMAN, P01111
    Similarity: Belongs to the small GTPase superfamily. Ras 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: RASN_HUMAN, P01111
    Function: Ras proteins bind GDP/GTP and possess intrinsic GTPase activity
    Enzyme regulation: Alternate between an inactive form bound to GDP and an active form bound to GTP. Activated by a
    guanine nucleotide-exchange factor (GEF) and inactivated by a GTPase-activating protein (GAP)

         Genatlas biochemistry entry for NRAS:
    neuroblastoma Ras viral (v-ras) oncogene homolog

    miRNA
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    miRTarBase miRNAs that target NRAS:
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    OriGene 3'-UTR Clone: NRAS
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    8/81 QIAGEN miScript miRNA Assays for microRNAs that regulate NRAS (see all 81):
    hsa-miR-146a hsa-miR-218-1* hsa-miR-1304 hsa-miR-3150b-3p hsa-miR-510 hsa-miR-3148 hsa-miR-27a hsa-let-7i
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    Gene Ontology (GO): 3 molecular function terms (GO ID links to tree view):    About this table

    GO IDQualified GO termEvidencePubMed IDs
    GO:0003924GTPase activity IEA--
    GO:0005515protein binding ----
    GO:0005525GTP binding IEA--


    NRAS for ontologies           About GeneDecksing


    2 GenomeRNAi human phenotypes for NRAS:
     Decreased Wnt reporter activit  Decreased focal adhesion (FA)  

    Animal Models:
         Mouse knock-outs for NRAS: Nrastm1Rak Nrastm1Mok
         15 MGI mutant phenotypes (inferred from 5 alleles(MGI details for Nras):
     cardiovascular system  cellular  digestive/alimentary  embryogenesis  growth/size 
     hematopoietic system  homeostasis/metabolism  immune system  integument  limbs/digits/tail 
     liver/biliary system  mortality/aging  normal  tumorigenesis  vision/eye 

    NRAS 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

    Unified GeneCards pathways - 5/92 super-pathways (see all 92About this table 
    See pathways by source

    Super-pathwaycontained gene-specific pathways
    1SHC-mediated signalling
    8/13 pathways (see all 13)
    SHC-mediated signalling1.00
    MEK activation0.47
    SHC-related events0.88
    RAF phosphorylates MEK0.47
    SHC-related events triggered by IGF1R0.83
    RAF activation0.33
    SHC1 events in EGFR signaling0.76
    EGFR Transactivation by Gastrin0.26
    2Signaling by FGFR
    8/12 pathways (see all 12)
    Signaling by FGFR1.00
    DAP12 signaling0.83
    Downstream signaling of activated FGFR0.92
    Signaling by EGFR in Cancer0.83
    Signaling by FGFR in disease0.91
    DAP12 interactions0.76
    Signaling by ERBB20.89
    Signaling by PDGF0.72
    3ErbB4 Pathway
    8/12 pathways (see all 12)
    ErbB4 Pathway1.00
    Thrombopoietin Pathway0.43
    ErbB Family Pathway0.59
    LPS Stimulated MAPK Signaling0.36
    Prolactin Signaling0.54
    VEGF Signaling Pathway0.35
    ErbB2-ErbB3 Heterodimers0.47
    TREM1 Pathway0.32
    4IRS-related events
    IRS-related events1.00
    Signaling by Type 1 Insulin-like Growth Factor 1 Receptor (IGF1R)0.90
    IRS-mediated signalling0.98
    IGF1R signaling cascade0.90
    Insulin receptor signalling cascade0.94
    Signaling by Insulin receptor0.74
    IRS-related events triggered by IGF1R0.93
    5GPCR Pathway
    GPCR Pathway1.00
    Estrogen Pathway0.55
    Ras Pathway0.62
    Paxillin Interactions0.53
    Breast Cancer Regulation by Stathmin10.58
    P2Y Receptor Signaling0.38

    Pathway sources
    See GeneCards unified pathways
    Show all pathways

    4 EMD Millipore Pathways for NRAS
        Development EGFR signaling via small GTPases
    G-protein signaling N-RAS regulation pathway
    Development EPO-induced MAPK pathway
    G-protein signaling Ras family GTPases in kinase cascades (scheme)

    5/109 Downloadable PowerPoint Slides of QIAGEN Pathway Central Maps for NRAS (see all 109)
        Fc-GammaR Pathway
    Molecular Mechanisms of Cancer
    eIF2 Pathway
    Intracellular Calcium Signaling
    CDK5 Pathway

    5 Tocris Bioscience Pathways for NRAS
        Insulin Pathway
    Apoptosis Pathway
    TGF-beta Pathway
    NF-kappaB Pathway
    VEGF Pathway

    4 GeneGo (Thomson Reuters) Pathways for NRAS
        Development EPO-induced MAPK pathway
    G-protein signaling Ras family GTPases in kinase cascades (scheme)
    Development EGFR signaling via small GTPases
    G-protein signaling N-RAS regulation pathway

    5/7 BioSystems Pathways for NRAS (see all 7
        G Protein Signaling Pathways
    MAPK signaling pathway
    Signaling Pathways in Glioblastoma
    EGFR1 Signaling Pathway
    Regulation of Actin Cytoskeleton

    5/65        Reactome Pathways for NRAS (see all 65)
        SHC-related events
    EGFR Transactivation by Gastrin
    p38MAPK events
    SHC-mediated signalling
    IRS-mediated signalling

    5 PharmGKB Pathways for NRAS
        Bisphosphonate Pathway, Pharmacodynamics
    EGFR Inhibitor Pathway, Pharmacodynamics
    Sorafenib Pharmacodynamics
    VEGF Signaling Pathway
    Vemurafenib Pathway, Pharmacodynamics

    5/31         Kegg Pathways  (Kegg details for NRAS) (see all 31):
        MAPK signaling pathway
    ErbB signaling pathway
    Chemokine signaling pathway
    Axon guidance
    VEGF signaling pathway


    NRAS for pathways           About GeneDecksing

    Interactions:

        SABiosciences Gene Network CentralTM Interacting Genes and Proteins Network for NRAS

    STRING Interaction Network Preview (showing 5 interactants - click image to see 25)

    5/165 Interacting proteins for NRAS (P011112, 3 ENSP000003585484) via UniProtKB, MINT, STRING, and/or I2D (see all 165)
    InteractantInteraction Details
    GeneCardExternal ID(s)
    PLCE1Q9P2122, 3, ENSP000002607664MINT-65550 I2D: score=5 STRING: ENSP00000260766
    BCL2P104153, ENSP000003296234I2D: score=2 STRING: ENSP00000329623
    DNAJB1P256853, ENSP000002543224I2D: score=2 STRING: ENSP00000254322
    PIK3CAP423363, ENSP000002639674I2D: score=2 STRING: ENSP00000263967
    RASSF5Q8WWW03, ENSP000003474434I2D: score=2 STRING: ENSP00000347443
    About this table

    Gene Ontology (GO): 5/19 biological process terms (GO ID links to tree view) (see all 19):    About this table

    GO IDQualified GO termEvidencePubMed IDs
    GO:0000165MAPK cascade TAS--
    GO:0000186activation of MAPKK activity TAS--
    GO:0007173epidermal growth factor receptor signaling pathway TAS--
    GO:0007264small GTPase mediated signal transduction TAS--
    GO:0007265Ras protein signal transduction TAS--


    NRAS 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

    NRAS for compounds           About GeneDecksing

    Browse Small Molecules at EMD Millipore
    Browse drugs & compounds from Enzo Life Sciences

    Browse Tocris compounds for NRAS

    1 HMDB Compound for NRAS    About this table
    CompoundSynonyms CAS #PubMed Ids
    Guanosine triphosphate5'-GTP (see all 10)86-01-1--
    3 Novoseek chemical compound relationships for NRAS gene    About this table
    Compound   -log (P-Val)   Hits   PubMed IDs for Articles with Shared Sentences (# sentences)
    tyrosine 16.1 5 18450602 (2), 16467864 (1), 16281072 (1)
    oligonucleotide 0 1 8255093 (1)
    agar 0 1 16462768 (1)

    Search CenterWatch for drugs/clinical trials and news about NRAS / RASN 

    (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,
    siRNAs from OriGene, QIAGEN, shRNA from OriGene, microRNA from QIAGEN,
    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 NRAS gene: 
    NM_002524.4  

    Unigene Cluster for NRAS:

    Neuroblastoma RAS viral (v-ras) oncogene homolog
    Hs.486502  [show with all ESTs]
    Unigene Representative Sequence: NM_002524
    1 Ensembl transcript including schematic representation, and UCSC links where relevant:
    ENST00000369535(uc009wgu.3)

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      QIAGEN QuantiFast Probe-based Assays in human, mouse, rat NRAS

    Additional cDNA sequence: 

    AF493919.1 AY941100.1 AY941101.1 BC005219.1 BC013214.1 BT019734.1 BT019735.1 X02751.1 

    11 DOTS entries:

    DT.40115049  DT.100693486  DT.100811463  DT.121460043  DT.92360379  DT.100693463  DT.121460084  DT.121459944 
    DT.121460006  DT.91838834  DT.92474389 

    24/1776 AceView cDNA sequences (see all 1776):

    BE858061 BP365024 AW304909 BU509480 AA780939 AI339397 BF979096 AW028940 
    BE748331 AA665567 AI475111 BP358982 BM667890 AU123547 CB177844 BQ433939 
    CA394488 AA034186 BP359705 BX352858 BM696520 BG504488 AA916152 BF969612 

    GeneLoc Exon Structure


    (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

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

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

    About this image

    NRAS expression in embryonic tissues and stem cells
    Expression by the Database of Embryonic development, Stem cell research, and Regenerative medicine    About this table
    1 LifeMap In Vivo Development Anatomical Compartment/Cell 
    Tissue Anatomical Compartment CellCategory (developmental path)
    LungLung BudLung
    Expression: Positive    Negative     Selective marker
    Experimental details: Curated     Microarrays     In-situ hybridization

    See NRAS Protein Expression from SPIRE MOPED and PaxDB
    Genevestigator expression for NRAS

    SOURCE GeneReport for Unigene cluster: Hs.486502
        SABiosciences Expression via Pathway-Focused PCR Arrays including NRAS (see all 8): 
              mTOR Signaling in human mouse rat
              Oncogenes & Tumor Suppressor Genes in human mouse rat
              VEGF Signaling in human mouse rat
              Liver Cancer in human mouse rat
              Cancer Drug Targets 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 common ancestor of animals.

    Orthologs for NRAS gene from 6/23 species (see all 23)    About this table
    Organism Taxonomic
    classification
    Gene Description Human
    Similarity
    Orthology
    Type
    Details
    chicken
    (Gallus gallus)
    Aves NRAS1 neuroblastoma RAS viral (v-ras) oncogene homolog 81.13(n)
    96.83(a)
      419885  NM_001012549.1  NP_001012567.1 
    lizard
    (Anolis carolinensis)
    Reptilia NRAS6
    --
    94(a)
    1 ↔ 1
    4(130382670-130387371)
    African clawed frog
    (Xenopus laevis)
    Amphibia Xl.8952 African clawed frog N-ras mRNA, complete cds 79.19(n)    M97960.1 
    zebrafish
    (Danio rerio)
    Actinopterygii NM_131145.12   -- 79.79(n)   30380  NM_131145.1 
    fruit fly
    (Drosophila melanogaster)
    Insecta Ras85D3 eggshell pattern formation RAS small
    monomeric more
    85(a)   3 85D21   --
    worm
    (Caenorhabditis elegans)
    Secernentea C08F8.73 RAS-related protein 45(a)   IV(11177461-11178071)   --


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

    (Paralogs according to 1HomoloGene,
    2Ensembl, and 3SIMAP, Pseudogenes according to 4Pseudogene.org Build 68)
    About This Section
    Paralogs for NRAS gene
    REM12  RALA2  RIT22  RIT12  RRAS2  ERAS2  RALB2  RRAD2  
    REM22  KRAS2  GEM2  RRAS22  HRAS2  MRAS2  
    18/97 SIMAP similar genes for NRAS using alignment to 2 protein entries:     RASN_HUMAN (see all proteins) (see all similar genes):
    N-ras    c-bas/has    HRAS    KRAS    RALA    RAP1B
    RAP2A    RIT2    RALB    RAP1A    RIT1    RRAS2
    RAB1C    RAP2C    RAB1B    DKFZp547A0616    RAP2B    RRAS

    NRAS for paralogs           About GeneDecksing



    (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

    10/245 NCBI SNPs in NRAS are shown (see all 245    About this table
    Genomic DataTranscription Related DataAllele Frequencies
    SNP IDValidClinical
    significance
    Chr 1 posSequence#AA
    Chg
    TypeMore#Allele
    freq
    PopTotal
    sample
    More
    ----------
    rs115542901,2
    C,Hother113114988(-) TGGACA/C/G/
            
    AGAAG
    4 Q P R L mis16NS EA NA 408
    rs1219132481,2
    C,other113117189(-) AAAGCA/C/GCACTG 3 T P A mis10--------
    rs1214345961,2
    Cother113117203(-) AGGTGA/C/G/
            
    TGTTG
    4 D A G V mis10--------
    rs1214345951,2
    Cother113117204(-) CAGGTA/C/G/
            
    GTGTT
    4 S R G C mis10--------
    rs1219132371,2
    Cother113117206(-) AGCAGA/C/G/
            
    TGGTG
    4 D A G V mis10--------
    rs1219132501,2
    Cother113117207(-) GAGCAA/C/G/
            
    GTGGT
    4 S R G C mis10--------
    rs729944401,2
    C,--113105823(+) TCCCTC/ACAGAG 1 -- ut312Minor allele frequency- A:0.05WA 120
    rs115529811,2
    C--113105837(+) AGTTCA/GTACAA 1 -- ut312Minor allele frequency- G:0.00NA 4
    rs558131391,2
    C--113105889(+) ACGTTC/TTGAAA 1 -- ut310--------
    rs729944411,2
    C,--113105970(+) ATTGTG/CTGGCA 1 -- ut312Minor allele frequency- C:0.05WA 120

    HapMap Linkage Disequilibrium report for NRAS (115247078 - 115259515 bp)
    Structural Variations (Copy Number Variations, Insertions/Deletions, Inversions)
    Database of Genomic Variants (DGV): 3 variations for NRAS
         3 CNVs: 2322 3306 64651
    Human Gene Mutation Database (HGMD): NRAS

    5/19 SABiosciences Cancer Mutation PCR Assays for NRAS (see all 19):
    Cosmic IdAA Change
    581p.Q61E
    577p.A18T
    570p.G13C
    583p.Q61L
    575p.G13A
    5/32 SABiosciences Cancer Mutation PCR Arrays containing NRAS (see all 32):
    Breast Cancer
    Cancer Comprehensive Panel 384HT
    Lung Cancer
    Liver Cancer
    2 SABiosciences qBiomarker Copy Number PCR Arrays containing NRAS:
    Oncogenes & Tumor Suppressor Genes 384HC
    Prostate Cancer
    QIAGEN SeqTarget long-range PCR primers in human, mouse, rat for resequencing NRAS
    DNA2.0 Custom Variant and Variant Library Synthesis for NRAS

    (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

    NRAS for disorders           About GeneDecksing

    OMIM gene information: 164790   
    OMIM disorders: 114500  188470  613224  
    UniProtKB/Swiss-Prot: RASN_HUMAN, P01111
  • Defects in NRAS are a cause of juvenile myelomonocytic leukemia (JMML) [MIM:607785]. JMML is a pediatric
  • myelodysplastic syndrome that constitutes approximately 30% of childhood cases of myelodysplastic syndrome (MDS) and
    2% of leukemia
  • Defects in NRAS are the cause of Noonan syndrome type 6 (NS6) [MIM:613224]. A syndrome characterized by facial
  • dysmorphic features such as hypertelorism, a downward eyeslant and low-set posteriorly rotated ears. Other features
    can include short stature, a short neck with webbing or redundancy of skin, cardiac anomalies, deafness, motor delay
    and variable intellectual deficits
  • Defects in NRAS are the cause of autoimmune lymphoproliferative syndrome type 4 (ALPS4) [MIM:614470]. A
  • disorder of apoptosis, characterized by chronic accumulation of non-malignant lymphocytes, defective lymphocyte
    apoptosis, and an increased risk for the development of hematologic malignancies

    20/80 diseases for NRAS (see all 80):    About MalaCards
    juvenile myelomonocytic leukemia    autoimmune lymphoproliferative syndrome    myelomonocytic leukemia    lymphoproliferative syndrome
    noonan syndrome    malignant peripheral nerve sheath tumor    leukemia    autoimmune lymphoproliferative syndrome type iv
    thyroid cancer    paroxysmal nocturnal hemoglobinuria    thyroiditis    spitz nevus
    neuroblastoma    noonan syndrome 6    bone marrow cancer    familial adenomatous polyposis
    soft tissue sarcoma    nevus    gastrointestinal stromal tumor    plasma cell leukemia

    15 diseases from the University of Copenhagen DISEASES database for NRAS:
    Colorectal cancer     Carcinoma     Lung cancer     Pancreatic cancer
    Adenoma     Melanoma     Noonan syndrome     Leukemia
    Pancreatitis     Endometrial cancer     Gallbladder cancer     Familial adenomatous polyposis
    Lynch syndrome     Ovarian cancer     Bone marrow cancer

    10/21 Novoseek disease relationships for NRAS gene (see all 21)    About this table

    Disease   -log (P-Val)   Hits   PubMed IDs for Articles with Shared Sentences (# sentences)
    juvenile myelomonocytic leukemia 84.9 1 20471511 (1)
    melanoma 77.3 114 15917418 (5), 18227705 (5), 18375819 (4), 19509136 (4) (see all 41)
    preleukemia 73 1 7949098 (1)
    somatic mutations 65.4 6 15188009 (1), 10216104 (1), 20096196 (1), 17507627 (1) (see all 6)
    myelodysplastic syndromes 64.7 4 15257941 (2), 15474158 (1), 9379676 (1)
    nevi 61.6 8 16845322 (2), 17518771 (1), 17507627 (1)
    leukemogenesis 59.3 1 9680114 (1)
    nevi melanocytic 55 2 16845322 (1), 15009714 (1)
    uveal melanoma 53.3 1 14522897 (1)
    metastatic melanoma 51.6 2 14695152 (1), 17518771 (1)

    Genetic Association Database (GAD): NRAS
    Human Genome Epidemiology (HuGE) Navigator: NRAS (62 documents)
    Tumor Gene Database (TGDB): NRAS

    Export disorders for NRAS 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 NRAS gene, integrated from 9 sources (see all 305):
    (articles sorted by number of sources associating them with NRAS)
        Utopia: connect your pdf to the dynamic
    world of online information

    1. BRAF and NRAS mutations are frequent in nodular melanoma but are not associated with tumor cell proliferation or patient survival. (PubMed id 16098042)1, 4, 9 Akslen L.A....Kumar R. (2005)
    2. A restricted spectrum of NRAS mutations causes Noonan syndrome. (PubMed id 19966803)1, 2 Cirstea I.C.... Zenker M. (2010)
    3. NRAS mutation causes a human autoimmune lymphoproliferative syndrome. (PubMed id 17517660)1, 2 Oliveira J.B.... Lenardo M.J. (2007)
    4. DHHC9 and GCP16 constitute a human protein fatty acyltransferase with specificity for H- and N-Ras. (PubMed id 16000296)1, 2 Swarthout J.T.... Linder M.E. (2005)
    5. An acylation cycle regulates localization and activity of palmitoylated Ras isoforms. (PubMed id 15705808)1, 2 Rocks O....Bastiaens P.I.H. (2005)
    6. Nucleophosmin gene mutations are predictors of favorable prognosis in acute myelogenous leukemia with a normal karyotype. (PubMed id 16076867)1, 4 Schnittger S....Falini B. (2005)
    7. Ras gene mutations in patients with acute myeloid leukaemia and exposure to chemical agents. (PubMed id 14688017)1, 4 Barletta E....Costantini A.S. (2004)
    8. 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. (2004)
    9. Transforming genes from familial adenomatous polyposis patient cells detected by a tumorigenicity assay. (PubMed id 1970154)1, 2 Yuasa Y.... Tonomura A. (1990)
    10. All ras proteins are polyisoprenylated but only some are palmitoylated. (PubMed id 2661017)1, 2 Hancock J.F.... Marshall C.J. (1989)

    (in PubMed, OMIM, and NCBI Bookshelf)
    About This Section
     ANDOR
    Aliases
    Disorders
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      Query String
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      (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: 4893 HGNC: 7989 AceView: NRASandUNR Ensembl:ENSG00000213281 euGenes: HUgn4893
    ECgene: NRAS Kegg: 4893 H-InvDB: NRAS

    (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 NRAS Pharmacogenomics, SNPs, Pathways
    ATLAS Chromosomes in Cancer entry for NRAS Genetics and Cytogenetics in Oncology and Haematology
    NRASbasehttp://bioinf.uta.fi/NRASbase/
    NIEHS-SNPshttp://egp.gs.washington.edu/data/nras/
    Wikipedia http://en.wikipedia.org/wiki/RAS_proteins

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

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



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     Regulatory tfbs in NRAS promoter
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