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

NGRN Gene

protein-coding   GIFtS: 47
GCID: GC15P090808

neugrin, neurite outgrowth associated
 Explore 10 diseases affiliated with
NGRN via
MalaCards
our new
 Human Malady Compendium 
Biological research products
for NGRN    

Aliases
for NGRN gene

(According to 1HGNC, 2Entrez Gene,
3UniProtKB/Swiss-Prot, 4UniProtKB/TrEMBL, 5OMIM, 6GeneLoc, 7Ensembl, 8DME, 9miRBase, and/or 10fRNAdb)
About This Section
This gene clusters with an RNA gene
Subcategory (RNA class): lncRNA

Quality score for the ORGUL clustered with this gene is 3

Aliases
Neugrin, Neurite Outgrowth Associated1 2     Spinal Cord-Derived Protein FI58G2 3
DSC921 2     Neugrin1
Mesenchymal Stem Cell Protein DSC922 3     Neurite Outgrowth Associated Protein2
Neurite Outgrowth-Associated Protein2 3     FI58G3

External Ids:    HGNC: 180771   Entrez Gene: 513352   Ensembl: ENSG000001827687   UniProtKB: Q9NPE23   
ORGUL members:         
NONCODE:n408119    

Export aliases for NGRN gene to outside databases

Previous GC identifers: GC15P088596 GC15P088609 GC15P066920


Summaries
for NGRN gene

(According to Entrez Gene, Tocris Bioscience, Wikipedia's Gene Wiki, PharmGKB,
UniProtKB/Swiss-Prot, and/or UniProtKB/TrEMBL)
About This Section
UniProtKB/Swiss-Prot: NGRN_HUMAN, Q9NPE2
Function: May be involved in neuronal differentiation




Genomic Views
for NGRN 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 69), Regulatory elements and Epigenetics data according to QIAGEN, SABiosciences, and/or SwitchGear Genomics)
About This Section
RefSeq DNA sequence:
NC_000015.9  NC_018926.1  NT_010274.17  
Regulatory elements:
   SABiosciences Regulatory transcription factor binding sites in the NGRN gene promoter:
         HOXA3   Brachyury   YY1   CREB   CP2   POU2F1   deltaCREB   c-Myb   NF-Y   CBF(2)   
         Other transcription factors

SwitchGear Promoter luciferase reporter plasmid: NGRN promoter sequence
   Search SABiosciences Chromatin IP Primers for NGRN

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


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

Entrez Gene cytogenetic band: 15q26.1   Ensembl cytogenetic band:  15q26.1   HGNC cytogenetic band: 15q26.1

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

GeneLoc information about chromosome 15         GeneLoc Exon Structure

GeneLoc location for GC15P090808:  view genomic region     (about GC identifiers)

Start:
 90,808,891 bp from pter      End:
 90,816,463 bp from pter
Size:
 7,573 bases      Orientation:
 plus strand

Proteins
for NGRN gene

(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: NGRN_HUMAN, Q9NPE2 (See protein sequence)
Recommended Name: Neugrin precursor  
Size: 291 amino acids; 32408 Da
Subcellular location: Nucleus. Secreted (Potential)
Sequence caution: Sequence=AAF65447.1; Type=Erroneous translation; Note=Wrong choice of CDS; Sequence=AAG09725.1;
Type=Erroneous translation; Note=Wrong choice of CDS; Sequence=AAG09725.1; Type=Frameshift; Positions=47;
Sequence=AAH01682.1; Type=Erroneous translation; Note=Wrong choice of CDS; Sequence=AAH07222.1; Type=Erroneous
translation; Note=Wrong choice of CDS; Sequence=AAH09389.1; Type=Erroneous translation; Note=Wrong choice of CDS;
Sequence=AAH17192.1; Type=Erroneous translation; Note=Wrong choice of CDS; Sequence=BAB21533.1; Type=Erroneous
translation; Note=Wrong choice of CDS; Sequence=BAB21533.1; Type=Frameshift; Positions=47; Sequence=BAG35525.1;
Type=Erroneous translation; Note=Wrong choice of CDS; Sequence=BAG35525.1; Type=Miscellaneous discrepancy;
Note=N-terminus does not match isoform 2; Sequence=CAB96088.1; Type=Erroneous translation; Note=Wrong choice of CDS;
Sequence=CAD39160.1; Type=Erroneous translation; Note=Wrong choice of CDS;
Secondary accessions: B2R6M8 Q4V9L7 Q9HBL4
Alternative splicing: 2 isoforms:  Q9NPE2-2   Q9NPE2-3   (May be produced at very low levels due to a premature stop codon in the mRNA, leading to nonsense-mediated mRNA decay)

Explore the universe of human proteins at neXtProt for NGRN: NX_Q9NPE2

Post-translational modifications:

  • View modification sites using PhosphoSitePlus2
  • View neXtProt modification sites for NX_Q9NPE2

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

    REFSEQ proteins: NP_001028260.2  
    ENSEMBL proteins: 
     ENSP00000368389  

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    Uscn Proteins for NGRN

    Gene Ontology (GO): 2 cellular component terms (GO ID links to tree view):    About this table

    GO IDQualified GO termEvidencePubMed IDs
    GO:0005576extracellular region IEA--
    GO:0005634nucleus NAS11118320


    NGRN for ontologies           About GeneDecksing



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    Uscn ELISAs and CLIAs for NGRN

    Protein Domains /
    Families
    for NGRN gene

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

    1 InterPro domain/family:
     IPR010487 Neugrin-related

    Graphical View of Domain Structure for InterPro Entry Q9NPE2

    ProtoNet protein and cluster: Q9NPE2

    UniProtKB/Swiss-Prot: NGRN_HUMAN, Q9NPE2
    Similarity: Belongs to the neugrin family


    Function
    for NGRN gene

    (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: NGRN_HUMAN, Q9NPE2
    Function: May be involved in neuronal differentiation
    Induction: Highly up-regulated in neuroblastostoma cells by retinoic acid treatment inducing neurite outgrowth

    miRNA
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    2 QIAGEN miScript miRNA Assays for microRNAs that regulate NGRN:
    hsa-miR-124* hsa-miR-4255
    SwitchGear 3'UTR luciferase reporter plasmid: NGRN 3' UTR sequence
    Inhib. RNA
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    OriGene shRNA RFP: NGRN
    OriGene siRNA: NGRN
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    Gene Editing
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    Clone
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    In Situ Assay
    Products:       
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    Gene Ontology (GO): 1 molecular function term (GO ID links to tree view):    About this table

    GO IDQualified GO termEvidencePubMed IDs
    GO:0003674molecular_function ND--


    NGRN for ontologies           About GeneDecksing


    1 GenomeRNAi human phenotype for NGRN:
     Increased HPV18 LCR reporter a 

    Animal Models:
         1 MGI mutant phenotype (inferred from 1 allele) (MGI details for Ngrn):
     mortality/aging 

    NGRN for phenotypes           About GeneDecksing


    Pathways & Interactions
    for NGRN gene

    (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:

        Search SABiosciences Gene Network CentralTM Interacting Genes and Proteins Networks for NGRN

    STRING Interaction Network Preview (showing 3 interactants - click image to see more details)

    5/233 Interacting proteins for NGRN (Q9NPE22, 3 ENSP000003683894) via UniProtKB, MINT, STRING, and/or I2D (see all 233)
    InteractantInteraction Details
    GeneCardExternal ID(s)
    ICT1Q141972, 3, ENSP000003015854MINT-8079030 I2D: score=1 STRING: ENSP00000301585
    E2F1Q010943I2D: score=1 
    AARS2Q5JTZ92MINT-8079030
    AASSQ9UDR52MINT-8079030
    ABCB7O750272MINT-8079030
    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:0030182neuron differentiation NAS11118320


    NGRN for ontologies           About GeneDecksing



    Drugs & Compounds
    for NGRN gene

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

    Browse Tocris compounds for NGRN
    Search CenterWatch for drugs/clinical trials and news about NGRN 

    Transcripts
    for NGRN gene

    (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 NGRN gene (2 alternative transcripts): 
    NM_016645.2  NM_001033088.1  

    Unigene Cluster for NGRN:

    Neugrin, neurite outgrowth associated
    Hs.743961  [show with all ESTs]
    Unigene Representative Sequence: AB029315
    2 Ensembl transcripts including schematic representations, and UCSC links where relevant:
    ENST00000331497(uc002bpf.1 uc002bpg.1) ENST00000379095

    miRNA
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    2 QIAGEN miScript miRNA Assays for microRNAs that regulate NGRN:
    hsa-miR-124* hsa-miR-4255
    SwitchGear 3'UTR luciferase reporter plasmid: NGRN 3' UTR sequence
    Inhib. RNA
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    Clone
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    Primer
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    Additional cDNA sequence: 

    AB029315.1 AF225423.1 AF242770.1 AK312641.1 AL355699.1 AL355700.1 AL360142.1 AL834503.1 
    AY049780.1 BC001682.2 BC007222.1 BC009389.2 BC017192.2 BC019023.2 BC096824.1 NR_028052.1 

    24/25 DOTS entries (see all 25):

    DT.95200729  DT.100880913  DT.101985414  DT.449823  DT.91772111  DT.100880916  DT.100038836  DT.100880912 
    DT.100801763  DT.100880910  DT.95362694  DT.100034260  DT.100813545  DT.100880908  DT.121026743  DT.100880906 
    DT.91772117  DT.100679017  DT.100830045  DT.102833461  DT.121026730  DT.91772122  DT.95200724  DT.121026781 

    24/864 AceView cDNA sequences (see all 864):

    BU615938 BQ000028 AI161434 BQ636817 AJ713069 BC009389 AI375357 AI356517 
    AV706815 BU069409 BU579797 W76636 AW615611 CR595022 BM876152 BU075739 
    NM_016645 AF242770 AA643075 AA856733 AI760542 BI829570 AI692848 BG113801 

    GeneLoc Exon Structure

    5/6 Alternative Splicing Database (ASD) splice patterns (SP) for NGRN (see all 6)    About this scheme

    ExUns: 1 ^ 2 ^ 3 ^ 4 ^ 5 ^ 6 ^ 7a · 7b ^ 8a · 8b ^ 9a · 9b ^ 10a · 10b ^ 11 ^ 12 ^ 13 ^ 14a · 14b · 14c ^ 15 ^ 16a · 16b · 16c
    SP1:                          -     -                       -     -                 -                       -     -     -                           
    SP2:                                                        -                                                                                       
    SP3:                                                                                                                                                
    SP4:                                                                                                                                                
    SP5:                                                                                                                                                


    ECgene alternative splicing isoforms for NGRN

    Expression
    for NGRN gene

    (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

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

    Microarray
    RNAseq (Illumina Body Map)
    (100×FPKM)½
    SAGE (Serial Analysis of Gene Expression)
    About this image
    See NGRN Protein Expression from SPIRE MOPED and PaxDB
    Genevestigator expression for NGRN

    SOURCE GeneReport for Unigene cluster: Hs.743961

    UniProtKB/Swiss-Prot: NGRN_HUMAN, Q9NPE2
    Tissue specificity: Expressed at high levels in heart, brain and skeletal muscle. In brain, mainly expressed in neurons
    rather than glial cells

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    In Situ
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    Orthologs
    for NGRN gene

    (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 chordates.

    Orthologs for NGRN gene from 2/7 species (see all 7)    About this table
    Organism Taxonomic
    classification    		 Gene Description Human
    Similarity    		 Orthology
    Type    		 Details
    mouse
    (Mus musculus)    		 Mammalia Ngrn1 , 5 neugrin, neurite outgrowth associated1, 5 79.31(n)1
    72.07(a)1    		   7 (45.58 cM)5
    834851  NM_031375.41  NP_113552.31 
     802612155 
    zebrafish
    (Danio rerio)    		 Actinopterygii si:ch211-199o1.51 si:ch211-199o1.5 48.69(n)
    41.2(a)    		   569275  NM_001045253.1  NP_001038718.1 


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

    Paralogs
    for NGRN gene

    (Paralogs according to 1HomoloGene,
    2Ensembl, and 3SIMAP, Pseudogenes according to 4Pseudogene.org Build 68)
    About This Section
    Paralogs for NGRN gene

    NGRN for paralogs           About GeneDecksing


    5 Pseudogenes.org Pseudogenes for NGRN
    PGOHUM00000247168 PGOHUM00000257064 PGOHUM00000250169 PGOHUM00000243243 PGOHUM00000260197


    Genomic Variants
    for NGRN gene

    (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

    10/171 NCBI SNPs in NGRN are shown (see all 171)     About this table
    Genomic DataTranscription Related DataAllele Frequencies
    SNP IDValidClinical
    significance    		Chr 15 posSequence#AA
    Chg    		TypeMore#Allele
    freq    		PopTotal
    sample    		More
    ----------
    rs1885548391,2
    		--90806918(+) TCCAAC/TGCTCC 2 -- us2k10--------
    rs1448723341,2
    		--90807138(+) AAGCAG/TGAATG 2 -- us2k10--------
    rs1490340421,2
    		--90807208(+) GAGCCA/GGCAGC 2 -- us2k10--------
    rs1927618961,2
    		--90807289(+) ACTAGC/TCGTAA 2 -- us2k10--------
    rs1429607881,2
    		--90807291(+) TAGCCC/GTAAGT 2 -- us2k10--------
    rs1166334351,2
    		C,F,--90807335(+) TAAATC/TCCACT 2 -- us2k11Minor allele frequency- T:0.02WA 118
    rs1511213951,2
    		--90807352(+) CATAGA/GGCTTG 2 -- us2k10--------
    rs752462931,2
    		--90807470(+) CAAGGC/ATGAAG 2 -- us2k11Minor allele frequency- A:0.50CSA 2
    rs1118052951,2
    		--90807691(+) AGCCAC/TCGCAC 2 -- us2k12Minor allele frequency- T:0.13CSA WA 120
    rs1164286521,2
    		--90807720(+) TCTGTA/GCACTA 2 -- us2k11Minor allele frequency- G:0.01WA 118

    HapMap Linkage Disequilibrium report for NGRN (90808891 - 90816463 bp)
    Structural Variations (Copy Number Variations, Insertions/Deletions, Inversions)
    Database of Genomic Variants (DGV): 2 variations for NGRN
         2 CNVs: 3094 8804

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    QIAGEN SeqTarget long-range PCR primers in human, mouse, rat for resequencing NGRN
    DNA2.0 Custom Variant and Variant Library Synthesis for NGRN

    Disorders / Diseases
    for NGRN gene

    (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
    NGRN for disorders           About GeneDecksing

    10 diseases for NGRN:    About MalaCards
    amyotrophic lateral sclerosis    lateral sclerosis    differentiating neuroblastoma    pancreatic ductal adenocarcinoma
    neuroblastoma    nasopharyngitis    adenocarcinoma    pancreatitis
    neuronitis    carcinoma

    1 Novoseek disease relationship for NGRN gene    About this table

    Disease   -log (P-Val)   Hits   PubMed IDs for Articles with Shared Sentences (# sentences)
    inflammation 16.1 2 15477757 (1)


    Export disorders for NGRN gene to outside databases

    Publications
    for NGRN gene

    (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 NGRN gene, integrated from 9 sources (see all 14):
    (articles sorted by number of sources associating them with NGRN)    		    Utopia: connect your pdf to the dynamic
    world of online information

    1. Two novel genes, human neugrin and mouse m-neugrin, are upregulated with neuronal differentiation in neuroblastoma cells. (PubMed id 11118320)1, 2, 3, 9 Ishigaki S.... Sobue G. (2000)
    2. A functional peptidyl-tRNA hydrolase, ICT1, has been recruited into the human mitochondrial ribosome. (PubMed id 20186120)1 Richter R....Chrzanowska-Lightowlers Z.M. (2010)
    3. Quantitative phosphoproteomics reveals widespread full phosphorylation site occupancy during mitosis. (PubMed id 20068231)2 Olsen J.V....Mann M. (2010)
    4. Two-hybrid analysis identifies PSMD11, a non-ATPase s ubunit of the proteasome, as a novel interaction partner of AMP-activated prote in kinase. (PubMed id 19616115)1 Moreno D....Sanz P. (2009)
    5. A quantitative atlas of mitotic phosphorylation. (PubMed id 18669648)2 Dephoure N.... Gygi S.P. (2008)
    6. The full-ORF clone resource of the German cDNA consortium. (PubMed id 17974005)2 Bechtel S.... Schupp I. (2007)
    7. Analysis of the DNA sequence and duplication history of human chromosome 15. (PubMed id 16572171)2 Zody M.C....Nusbaum C. (2006)
    8. The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC). (PubMed id 15489334)2 Gerhard D.S....Malek J. (2004)
    9. Complete sequencing and characterization of 21,243 full-length human cDNAs. (PubMed id 14702039)2 Ota T.... Sugano S. (2004)
    10. Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences. (PubMed id 12477932)1 Strausberg R.L....Marra M.A. (2002)

    External Searches for NGRN gene

    (in PubMed, OMIM, and NCBI Bookshelf)
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    Genome Databases showing NGRN gene

    (According to Entrez Gene, HGNC, AceView, euGenes, Ensembl, miRBase, ECgene, Kegg, and/or H-InvDB)
    About This Section
    Entrez Gene: 51335 HGNC: 18077 AceView: NEUGRIN Ensembl:ENSG00000182768 euGenes: HUgn51335
    ECgene: NGRN H-InvDB: NGRN

    Other Databases showing NGRN gene

    (According to HUGE)
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    Specialized Databases showing NGRN gene

    (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 NGRN Pharmacogenomics, SNPs, Pathways

    Intellectual Property
    for NGRN gene

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

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