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

NTNG1 Gene

protein-coding   GIFtS: 59
GCID: GC01P107682

netrin G1

 Explore 8 diseases affiliated with
NTNG1 via our new
 Human Malady Compendium 
Biological research products
for NTNG1
    

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

Aliases
Netrin G11 2     Laminet 12
KIAA09761 3 5     Laminet-13
Lmnt11 2     Netrin G1f2
LMNT13 5     Netrin-G11
YLSR5712     Laminet-13
Axon Guidance Molecule2     

External Ids:    HGNC: 233191   Entrez Gene: 228542   Ensembl: ENSG000001626317   OMIM: 6088185   UniProtKB: Q9Y2I23   

Export aliases for NTNG1 gene to outside databases

Previous GC identifers: GC00U990862 GC09P128391 GC01P107038 GC01P107395 GC01P107484 GC01P105628


(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 NTNG1:
Netrin G1 (NTNG1) belongs to a conserved family of proteins that act as axon guidance cues during vertebrate nervous
system development (Nakashiba et al., 2000 (PubMed 10964959)).(supplied by OMIM, Mar 2008)

UniProtKB/Swiss-Prot: NTNG1_HUMAN, Q9Y2I2
Function: Promotes neurite outgrowth of both axons and dendrites (By similarity)

Gene Wiki entry for NTNG1


(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 NTNG1 gene promoter:
         p53   NRSF form 1   NRSF form 2   
         Other transcription factors

SwitchGear Promoter luciferase reporter plasmidNTNG1 promoter sequence
   Search SABiosciences Chromatin IP Primers for NTNG1

Epigenetics:
QIAGEN PyroMark CpG Assay predesigned Pyrosequencing DNA Methylation assays in human, mouse, rat NTNG1


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

Entrez Gene cytogenetic band: 1p13.3   Ensembl cytogenetic band:  1p13.3   HGNC cytogenetic band: 1p13.2-p13.1

NTNG1 Gene in genomic location: bands according to Ensembl, locations according to (and/or Entrez Gene and/or Ensembl if different)
NTNG1 gene location

GeneLoc information about chromosome 1         GeneLoc Exon Structure

GeneLoc location for GC01P107682:  view genomic region     (about GC identifiers)

Start:
107,682,629 bp from pter      End:
108,026,080 bp from pter
Size:
343,452 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: NTNG1_HUMAN, Q9Y2I2 (See protein sequence)
Recommended Name: Netrin-G1 precursor  
Size: 539 amino acids; 60541 Da
Subunit: Interacts with NGL1
Subcellular location: Cell membrane; Lipid-anchor, GPI-anchor (By similarity)
Sequence caution: Sequence=BAA76820.2; Type=Erroneous initiation;
1 PDB 3D structure from and Proteopedia for NTNG1:
3ZYJ (3D)    
Secondary accessions: Q5VU86 Q5VU87 Q5VU89 Q5VU90 Q5VU91 Q7Z2Y3 Q8N633
Alternative splicing: 6 isoforms:  Q9Y2I2-3   Q9Y2I2-2   Q9Y2I2-1   Q9Y2I2-4   Q9Y2I2-5   Q9Y2I2-6   (No experimental confirmation available)

Explore the universe of human proteins at neXtProt for NTNG1: NX_Q9Y2I2

Post-translational modifications:

  • N-glycosylated (By similarity)1
  • View modification sites using PhosphoSitePlus2
  • View neXtProt modification sites for NX_Q9Y2I2

  • NTNG1 Protein expression data from MOPED and PaxDb:    About this image 
    Estimated protein expression log10 (pmol).

    REFSEQ proteins (3 alternative transcripts): 
    NP_055732.2  NP_001106697.1  NP_001106699.1  

    ENSEMBL proteins: 
     ENSP00000359093   ENSP00000359091   ENSP00000359085   ENSP00000294649   ENSP00000359084  
     ENSP00000359083   ENSP00000359082   ENSP00000359090   ENSP00000359088   ENSP00000440561  
     ENSP00000359078   ENSP00000359089   ENSP00000359087  

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    Novus Biologicals NTNG1 Lysates
    Browse Sino Biological Recombinant Proteins
    Browse ProSpec Recombinant Proteins
    Browse Proteins at Uscn

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

    GO IDQualified GO termEvidencePubMed IDs
    GO:0046658anchored to plasma membrane ISS--


    NTNG1 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

    NTNG1 for domains           About GeneDecksing

    4 InterPro domains/families:
     IPR000742 EG-like_dom
     IPR008211 Laminin_N
     IPR013032 EGF-like_CS
     IPR002049 EGF_laminin

    Graphical View of Domain Structure for InterPro Entry Q9Y2I2

    ProtoNet protein and cluster: Q9Y2I2

    1 Blocks protein family: IPB006210 Type I EGF

    UniProtKB/Swiss-Prot: NTNG1_HUMAN, Q9Y2I2
    Similarity: Contains 3 laminin EGF-like domains
    Similarity: Contains 1 laminin N-terminal domain


    (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: NTNG1_HUMAN, Q9Y2I2
    Function: Promotes neurite outgrowth of both axons and dendrites (By similarity)

    miRNA
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    hsa-miR-411* hsa-miR-579 hsa-miR-3194-5p hsa-miR-379* hsa-miR-30d hsa-miR-219-5p hsa-miR-632 hsa-miR-570
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    Inhib. RNA
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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:0005515protein binding IPI14595443


    NTNG1 for ontologies           About GeneDecksing


    Animal Models:
         Mouse knock-out Ntng1tm1Lex for NTNG1
         2 MGI mutant phenotypes (inferred from 2 alleles(MGI details for Ntng1):
     mortality/aging  nervous system 

    NTNG1 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  About this table 
    See pathways by source

    Super-pathwaycontained gene-specific pathways
    1Axon guidance
    Axon guidance1.00

    Pathway sources
    See GeneCards unified pathways
    Show all pathways



    1         Kegg Pathway  (Kegg details for NTNG1):
        Axon guidance


    NTNG1 for pathways           About GeneDecksing

    Interactions:

        Search SABiosciences Gene Network CentralTM Interacting Genes and Proteins Networks for NTNG1

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

    4 Interacting proteins for NTNG1 (Q9Y2I22, 3 ENSP000003590854) via UniProtKB, MINT, STRING, and/or I2D
    InteractantInteraction Details
    GeneCardExternal ID(s)
    LRRC4CQ9HCJ22, 3, ENSP000002781984MINT-8301036 MINT-8301082 MINT-8300711 MINT-8300986 I2D: score=2 STRING: ENSP00000278198
    LRRC4Q9HBW12MINT-8301004 MINT-8301057
    SLC25A24ENSP000002641284STRING: ENSP00000264128
    EWSR1ENSP000003810314STRING: ENSP00000381031
    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:0007409axonogenesis ISS--


    NTNG1 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
    Browse Small Molecules at EMD Millipore
    Browse drugs & compounds from Enzo Life Sciences

    Browse Tocris compounds for NTNG1
    Search CenterWatch for drugs/clinical trials and news about NTNG1 

    (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 NTNG1 gene (3 alternative transcripts): 
    NM_014917.2  NM_001113226.1  NM_001113228.1  

    Unigene Cluster for NTNG1:

    Netrin G1
    Hs.732535  [show with all ESTs]
    Unigene Representative Sequence: AB023193
    15 Ensembl transcripts including schematic representations, and UCSC links where relevant:
    ENST00000370076 ENST00000370074(uc009wem.3) ENST00000370068(uc001dvi.3 uc001dve.3 uc009wek.3)
    ENST00000294649(uc001dvd.1) ENST00000370067(uc001dvg.3) ENST00000462149
    ENST00000370066 ENST00000370065 ENST00000477948 ENST00000370073(uc001dvh.4 uc010out.2)
    ENST00000370071(uc001dvf.4 uc001dvc.4) ENST00000542803 ENST00000370061
    ENST00000370072 ENST00000370070

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    8/43 QIAGEN miScript miRNA Assays for microRNAs that regulate NTNG1 (see all 43):
    hsa-miR-411* hsa-miR-579 hsa-miR-3194-5p hsa-miR-379* hsa-miR-30d hsa-miR-219-5p hsa-miR-632 hsa-miR-570
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    Inhib. RNA
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    Additional cDNA sequence: 

    AB023193.1 AK296533.1 AK297659.1 AY358365.1 AY764260.1 AY764261.1 AY764262.1 AY764263.1 
    AY764264.1 AY764265.1 AY764266.1 AY764267.1 AY781194.1 BC030220.1 BX538348.1 

    6 DOTS entries:

    DT.433424  DT.40112231  DT.40191199  DT.121364449  DT.436509  DT.454290 

    24/51 AceView cDNA sequences (see all 51):

    CA395310 CK299898 AI140857 BX105933 BC030220 CR594836 AW241931 BX538348 
    BU728093 AI435585 BE699190 AA422028 AW085292 BP376410 AI524577 BQ876409 
    AY358365 AI858128 BP360442 AI742127 BI768535 AA218981 BM706705 BX377397 

    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

    NTNG1 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

    NTNG1 expression in embryonic tissues and stem cells
    Expression by the Database of Embryonic development, Stem cell research, and Regenerative medicine    About this table
    8 LifeMap In Vivo Development Anatomical Compartments/Cells 
    Tissue Anatomical Compartment CellCategory (developmental path)
    CartilageCervical Intervertebral DiscIntervertebral Disc Annulus Fibrosus CellsCartilage
    CartilageLumbar Intervertebral DiscIntervertebral Disc Annulus Fibrosus CellsCartilage
    CartilageSacral Intervertebral DiscIntervertebral Disc Annulus Fibrosus CellsCartilage
    CartilageThoracic Intervertebral DiscIntervertebral Disc Annulus Fibrosus CellsCartilage
    OvaryPrimary FollicleGranulosa CellsOvary
    OvaryPrimordial FolliclePre-Granulosa CellsOvary
    BoneMandibular ProcessBone
    CartilageLumbar Intervertebral DiscCartilage
    Expression: Positive    Negative     Selective marker
    Experimental details: Curated     Microarrays     In-situ hybridization
    Stem Cell Differentiation: 3 LifeMap Cells 
    NameCategory
    PureStem™ mesenchymal progenitor SM30 (Embryonic Progenitor Cell)Adipose, Bone, Cartilage
    PureStem™ progenitor F15 (Embryonic Progenitor Cell)
    N2/LSB/S/F8/CHIR-induced cells (Generation of midbra...)

    See NTNG1 Protein Expression from SPIRE MOPED and PaxDB
    Genevestigator expression for NTNG1

    SOURCE GeneReport for Unigene cluster: Hs.732535

    UniProtKB/Swiss-Prot: NTNG1_HUMAN, Q9Y2I2
    Tissue specificity: Highly expressed in the thalamus, with very low expression, if any, in other tissues

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    In Situ
    Assay Products:
     

     
    Advanced Cell Diagnostics RNAscope RNA in situ hybridization assays for NTNG1

    (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 NTNG1 gene from 3/12 species (see all 12)    About this table
    Organism Taxonomic
    classification
    Gene Description Human
    Similarity
    Orthology
    Type
    Details
    chicken
    (Gallus gallus)
    Aves NTNG11 netrin G1 77.28(n)
    80.25(a)
      424336  XM_001231446.2  XP_001231447.1 
    lizard
    (Anolis carolinensis)
    Reptilia LAMA26
    NTNG16
    --

    86(a)
    possible ortholog
    1 ↔ 1
    GL343315.1(754389-940168)
    4(83659320-83659949)
    zebrafish
    (Danio rerio)
    Actinopterygii ntng11 netrin G1 64.43(n)
    65.65(a)
      569075  XM_692438.5  XP_697530.5 


    ENSEMBL Gene Tree for NTNG1 (if available)
    TreeFam Gene Tree for NTNG1 (if available) 

    (Paralogs according to 1HomoloGene,
    2Ensembl, and 3SIMAP, Pseudogenes according to 4Pseudogene.org Build 68)
    About This Section
    Paralogs for NTNG1 gene
    NTN42  LAMA12  NTN52  LAMA32  LAMA22  LAMB22  LAMC12  LAMC22  
    LAMA52  NTN32  LAMB32  LAMC32  LAMA42  NTN12  USH2A2  LAMB42  
    LAMB12  NTNG22  
    5 SIMAP similar genes for NTNG1 using alignment to 14 protein entries:     NTNG1_HUMAN (see all proteins):
    NTNG2    VWDE    NELL1    NTN1    CRB1

    NTNG1 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

    10/5761 NCBI SNPs in NTNG1 are shown (see all 5761    About this table
    Genomic DataTranscription Related DataAllele Frequencies
    SNP IDValidClinical
    significance
    Chr 1 posSequence#AA
    Chg
    TypeMore#Allele
    freq
    PopTotal
    sample
    More
    ----------
    rs1148723071,2
    C,F,--107680699(+) AAGCTG/CGTTTA 2 -- us2k11Minor allele frequency- C:0.03WA 118
    rs1403650921,2
    --107680775(+) CCTTAC/TCACCT 3 -- us2k10--------
    rs1812230681,2
    --107680792(+) TGCTGA/GAGGAG 3 -- us2k10--------
    rs1157502871,2
    --107681070(+) TGATAC/TAGGAA 3 -- us2k11Minor allele frequency- T:0.01WA 118
    rs45422381,2
    H--107681102(+) CAAGAT/CTTTGA 3 -- us2k14Minor allele frequency- C:0.00NS EA 420
    rs1435521261,2
    --107681166(+) GTATAC/TTCCAG 3 -- us2k10--------
    rs1140898751,2
    --107681202(+) GATTTA/GTTTTA 3 -- us2k11Minor allele frequency- G:0.01NA 120
    rs127508681,2
    C,H--107681314(+) TGAGAA/CCTGTC 3 -- us2k14Minor allele frequency- C:0.00NS EA 420
    rs1853663421,2
    --107681329(+) TTTCAA/GGATCT 3 -- us2k10--------
    rs127299091,2
    H--107681364(+) AGAAGG/CCCACT 3 -- us2k14Minor allele frequency- C:0.00NS EA 418

    HapMap Linkage Disequilibrium report for NTNG1 (107682629 - 107932629 bp, first 250kb of NTNG1)
    Structural Variations (Copy Number Variations, Insertions/Deletions, Inversions)
    Database of Genomic Variants (DGV): 3 variations for NTNG1
         3 CNVs: 2318 48074 3304
    Human Gene Mutation Database (HGMD): NTNG1

    SABiosciences Cancer Mutation PCR Assays
    QIAGEN SeqTarget long-range PCR primers in human, mouse, rat for resequencing NTNG1
    DNA2.0 Custom Variant and Variant Library Synthesis for NTNG1

    (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.)
    About This Section

    NTNG1 for disorders           About GeneDecksing

    OMIM gene information: 608818    OMIM disorders: --

    8 diseases for NTNG1:    About MalaCards
    atypical rett syndrome    rett syndrome    anorexia nervosa    systemic lupus erythematosus
    lupus erythematosus    bipolar disorder    parkinson's disease    schizophrenia

    1 disease from the University of Copenhagen DISEASES database for NTNG1:
    Rett syndrome
    Genetic Association Database (GAD): NTNG1
    Human Genome Epidemiology (HuGE) Navigator: NTNG1 (13 documents)

    Export disorders for NTNG1 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 NTNG1 gene, integrated from 9 sources (see all 28):
    (articles sorted by number of sources associating them with NTNG1)
        Utopia: connect your pdf to the dynamic
    world of online information

    1. The DNA sequence and biological annotation of human chromosome 1. (PubMed id 16710414)1, 2 Gregory S.G.... Bentley D.R. (2006)
    2. Case-control association study of human netrin G1 gene in Japanese schizophrenia. (PubMed id 15508520)1, 4 Fukasawa M....Yoshikawa T. (2004)
    3. Fc receptor gamma subunit polymorphisms and systemic lupus erythematosus. (PubMed id 15494819)1, 4 Alansari A....Hajeer A.H. (2004)
    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. (2004)
    5. Signal peptide prediction based on analysis of experimentally verified cleavage sites. (PubMed id 15340161)1, 2 Zhang Z. and Henzel W.J. (2004)
    6. The secreted protein discovery initiative (SPDI), a large-scale effort to identify novel human secreted and transmembrane proteins: a bioinformatics assessment. (PubMed id 12975309)1, 2 Clark H.F.... Gray A.M. (2003)
    7. The netrin-G1 ligand NGL-1 promotes the outgrowth of thalamocortical axons. (PubMed id 14595443)1, 2 Lin J.C.... Rosenthal A. (2003)
    8. Netrin-G1: a novel glycosyl phosphatidylinositol-linked mammalian netrin that is functionally divergent from classical netrins. (PubMed id 10964959)1, 3 Nakashiba T....Itohara S. (2000)
    9. Prediction of the coding sequences of unidentified human genes. XIII. The complete sequences of 100 new cDNA clones from brain which code for large proteins in vitro. (PubMed id 10231032)1, 2 Nagase T.... Ohara O. (1999)
    10. Decreased mRNA expression of netrin-G1 and netrin-G2 in the temporal lobe in schizophrenia and bipolar disorder. (PubMed id 17507910)1, 9 Eastwood S.L. and Harrison P.J. (2008)

    (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)
    About This Section
    Entrez Gene: 22854 HGNC: 23319 AceView: NTNG1 Ensembl:ENSG00000162631 euGenes: HUgn22854
    ECgene: NTNG1 Kegg: 22854 H-InvDB: NTNG1

    (According to HUGE)
    About This Section
    HUGE: KIAA0976

    (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 NTNG1 Pharmacogenomics, SNPs, Pathways

    (Patent information from GeneIP,
    Licensable technologies from WIS Yeda, Salk, Tufts,
    IP news from LifeMap Sciences, Inc.)
    About This Section
    Patent Information for NTNG1 gene:
    Search GeneIP for patents involving NTNG1

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



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