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CLDN9 Gene

protein-coding   GIFtS: 54
GCID: GC16P003062

Claudin 9

  See CLDN9-related diseases
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
Claudin 91 2
claudin-92

External Ids:    HGNC: 20511   Entrez Gene: 90802   Ensembl: ENSG000002139377   UniProtKB: O954843   

Export aliases for CLDN9 gene to outside databases

Previous GC identifers: GC16P003083 GC16P003096 GC16P003064 GC16P003002 GC16P003035


(According to Entrez Gene, GeneCards, Tocris Bioscience, Wikipedia's Gene Wiki, PharmGKB,
UniProtKB/Swiss-Prot, and/or UniProtKB/TrEMBL)
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Entrez Gene summary for CLDN9 Gene:
This gene encodes a member of the claudin family. Claudins are integral membrane proteins and components of tight
junction strands. Tight junction strands serve as a physical barrier to prevent solutes and water from passing
freely through the paracellular space between epithelial or endothelial cell sheets, and also play critical roles
in maintaining cell polarity and signal transductions. This protein is one of the entry cofactors for hepatitis C
virus. Mouse studies revealed that this gene is required for the preservation of sensory cells in the hearing
organ and the gene deficiency is associated with deafness. (provided by RefSeq, Jun 2010)

GeneCards Summary for CLDN9 Gene:
CLDN9 (claudin 9) is a protein-coding gene. Diseases associated with CLDN9 include endolymphatic hydrops, and gastric adenocarcinoma. GO annotations related to this gene include structural molecule activity and identical protein binding. An important paralog of this gene is CLDN4.

UniProtKB/Swiss-Prot: CLD9_HUMAN, O95484
Function: Plays a major role in tight junction-specific obliteration of the intercellular space, through
calcium-independent cell-adhesion activity (By similarity)

Gene Wiki entry for CLDN9 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_000016.9  NC_018927.2  NT_010393.17  
Regulatory elements:
   Regulatory transcription factor binding sites in the CLDN9 gene promoter:
         COUP-TF1   AP-1   ATF-2   MyoD   COUP   HNF-4alpha2   HNF-4alpha1   COUP-TF   c-Jun   
         Other transcription factors

SwitchGear Promoter luciferase reporter plasmidCLDN9 promoter sequence
   Search Chromatin IP Primers for CLDN9

Epigenetics:
DNA Methylation CpG Assay Predesigned for Pyrosequencing in human, mouse, rat CLDN9


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

Entrez Gene cytogenetic band: 16p13.3   Ensembl cytogenetic band:  16p13.3   HGNC cytogenetic band: 16p13.3

CLDN9 Gene in genomic location: bands according to Ensembl, locations according to (and/or Entrez Gene and/or Ensembl if different)
CLDN9 gene location

GeneLoc information about chromosome 16         GeneLoc Exon Structure

GeneLoc location for GC16P003062:  view genomic region     (about GC identifiers)

Start:
3,062,457 bp from pter      End:
3,064,506 bp from pter
Size:
2,050 bases      Orientation:
plus 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., eBioscience, and/or antibodies-online,
Biochemical Assays by EMD Millipore, R&D Systems, OriGene, GenScript, Cell Signaling Technology, Enzo Life Sciences, Cloud-Clone Corp., eBioscience, and/or antibodies-online, Antibodies by EMD Millipore, R&D Systems, Cell Signaling Technology, OriGene, Novus Biologicals, Thermo Fisher Scientific, Abcam, Cloud-Clone Corp, antibodies-online, and/or others.)
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UniProtKB/Swiss-Prot: CLD9_HUMAN, O95484 (See protein sequence)
Recommended Name: Claudin-9  
Size: 217 amino acids; 22848 Da

Explore the universe of human proteins at neXtProt for CLDN9: NX_O95484

Explore proteomics data for CLDN9 at MOPED

Post-translational modifications: 

  • Modification sites at neXtProt
  • Modification sites at PhosphoSitePlus

  • See CLDN9 Protein Expression from SPIRE MOPED, PaxDB, and MaxQB

    REFSEQ proteins: NP_066192.1  
    ENSEMBL proteins: 
     ENSP00000398017  
    Reactome Protein details: O95484

    CLDN9 Human Recombinant Protein Products:

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    antibodies-online peptides for CLDN9

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    antibodies-online antibodies for CLDN9 (9 products) 

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    antibodies-online kits for CLDN9 (23 products) 


    (According to HGNC, IUPHAR, InterPro, ProtoNet, UniProtKB, and/or BLOCKS, Sets of similar genes according to GeneDecks)
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    HGNC Gene Families:
    CLDN: Claudins

    4 InterPro protein domains:
     IPR017974 Claudin_CS
     IPR003553 Claudin9
     IPR006187 Claudin
     IPR004031 PMP22/EMP/MP20/Claudin

    Graphical View of Domain Structure for InterPro Entry O95484

    ProtoNet protein and cluster: O95484

    2 Blocks protein domains:
    IPB003553 Claudin-9 signature
    IPB006187 Claudin family signature


    UniProtKB/Swiss-Prot: CLD9_HUMAN, O95484
    Similarity: Belongs to the claudin family


    Find genes that share domains with CLDN9           About GenesLikeMe


    (According to 1UniProtKB, Genatlas, LifeMap Discovery™, IUBMB, and/or 2DME, Human phenotypes from GenomeRNAi, Animal models from MGI Mar 06 2013, 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:

         UniProtKB/Swiss-Prot Summary: CLD9_HUMAN, O95484
    Function: Plays a major role in tight junction-specific obliteration of the intercellular space, through
    calcium-independent cell-adhesion activity (By similarity)

         Genatlas biochemistry entry for CLDN9:
    claudin 9,clostridium perfringens enterotoxin receptor,integral membrane protein,claudin family of major
    structural components of tight junction (TJ) strands

         Gene Ontology (GO): 2 molecular function terms:    About this table

    GO IDQualified GO termEvidencePubMed IDs
    GO:0005198structural molecule activity IEA--
    GO:0042802identical protein binding ISS--
         
    Find genes that share ontologies with CLDN9           About GenesLikeMe


    Phenotypes:
         3 MGI mutant phenotypes (inferred from 1 allele(MGI details for Cldn9):
     behavior/neurological  hearing/vestibular/ear  nervous system 

    Find genes that share phenotypes with CLDN9           About GenesLikeMe

    Animal Models:
       genOway: Develop your customized and physiologically relevant rodent model for CLDN9

    miRNA
    Products:
        
    miRTarBase miRNAs that target CLDN9:
    hsa-mir-186-5p (MIRT045011)

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    1 qRT-PCR Assays for microRNA that regulate CLDN9:
    hsa-miR-105
    SwitchGear 3'UTR luciferase reporter plasmidCLDN9 3' UTR sequence
    Inhib. RNA
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    Predesigned siRNA for gene silencing in human, mouse, rat CLDN9

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    (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
    CLD9_HUMAN, O95484: Cell junction, tight junction. Cell membrane; Multi-pass membrane protein
    Subcellular locations from COMPARTMENTS: 

    CompartmentConfidence
    plasma membrane5

    Gene Ontology (GO): 3 cellular component terms:    About this table

    GO IDQualified GO termEvidencePubMed IDs
    GO:0005886plasma membrane IEA--
    GO:0005923tight junction ISS--
    GO:0016021integral component of membrane IEA--

    Find genes that share ontologies with CLDN9           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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    SuperPaths for CLDN9 About   (see all 7)  
    See pathways by source

    SuperPathContained pathways About
    1Cell junction organization
    Cell junction organization0.70
    Cell-Cell communication0.64
    Cell-cell junction organization0.70
    Tight junction interactions0.51
    2Sertoli-Sertoli Cell Junction Dynamics
    Sertoli-Sertoli Cell Junction Dynamics0.38
    Epithelial Tight Junctions0.36
    3Integrin Pathway
    Transendothelial Migration of Leukocytes0.38
    4Tight junction
    Tight junction
    5Leukocyte transendothelial migration
    Leukocyte transendothelial migration


    Find genes that share SuperPaths with CLDN9           About GenesLikeMe

    Pathways by source                                                                                                                                                                 See SuperPaths
    Show all pathways

    3 Downloadable PowerPoint Slides of GeneGlobe Pathway Central Maps for CLDN9
        Sertoli-Sertoli Cell Junction Dynamics
    Epithelial Tight Junctions
    Transendothelial Migration of Leukocytes

    1 Reactome Pathway for CLDN9
        Tight junction interactions


    4 Kegg Pathways  (Kegg details for CLDN9):
        Cell adhesion molecules (CAMs)
    Tight junction
    Leukocyte transendothelial migration
    Hepatitis C

        Pathway & Disease-focused RT2 Profiler PCR Arrays including CLDN9: 
              Tight Junctions in human mouse rat
              Cell Junction PathwayFinder in human mouse rat

    Interactions:

        Search GeneGlobe Interaction Network for CLDN9

    Gene Ontology (GO): 4 biological process terms:    About this table

    GO IDQualified GO termEvidencePubMed IDs
    GO:0016338calcium-independent cell-cell adhesion ISS--
    GO:0034329cell junction assembly TAS--
    GO:0045216cell-cell junction organization TAS--
    GO:0070830tight junction assembly TAS--

    Find genes that share ontologies with CLDN9           About GenesLikeMe



    (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 CLDN9 (CLD9)

    1 HMDB Compound for CLDN9    About this table
    CompoundSynonyms CAS #PubMed Ids
    CalciumCa (see all 2)7440-70-2--



    (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 CLDN9 gene: 
    NM_020982.3  

    Unigene Cluster for CLDN9:

    Claudin 9
    Hs.296949  [show with all ESTs]
    Unigene Representative Sequence: NM_020982
    1 Ensembl transcript including schematic representation, and UCSC links where relevant:
    ENST00000445369(uc010uwo.1)
    miRNA
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    1 qRT-PCR Assays for microRNA that regulate CLDN9:
    hsa-miR-105
    SwitchGear 3'UTR luciferase reporter plasmidCLDN9 3' UTR sequence
    Inhib. RNA
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    Predesigned siRNA for gene silencing in human, mouse, rat CLDN9
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    Pre-validated RT2 qPCR Primer Assay in human, mouse, rat CLDN9
      QuantiTect SYBR Green Assays in human, mouse, rat CLDN9
      QuantiFast Probe-based Assays in human, mouse, rat CLDN9

    Additional mRNA sequence: 

    AK091002.1 AY390431.1 BC051870.1 BC065830.1 

    2 DOTS entries:

    DT.100711963  DT.40127055 

    2 AceView cDNA sequences:

    AY390431 AK091002 

    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™, 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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    CLDN9 expression in normal human tissues (normalized intensities)
    See probesets specificity/sensitivity at GeneAnnot
    About this imageBioGPS <intensity>2/3
    CGAP TAG: CCCTCCCAAC
    CLDN9 Expression
    About this image


    CLDN9 expression in embryonic tissues and stem cells    About this table
    Data from LifeMap, the Embryonic Development and Stem Cells Database
     selected tissues (see all 2) fully expand
     
     Bone (Muscoskeletal System)
             Zeugopod Epiphyseal End
     
     Head Mesenchyme (Muscoskeletal System)
             Frontonasal Process
    CLDN9 Protein expression data from MOPED1, PaxDb2 and MaxQB3    About this image

    CLDN9 Protein Expression

    SOURCE GeneReport for Unigene cluster: Hs.296949
        Pathway & Disease-focused RT2 Profiler PCR Arrays including CLDN9: 
              Tight Junctions in human mouse rat
              Cell Junction PathwayFinder in human mouse rat

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    In Situ
    Assay Products:
     

     
    Advanced Cell Diagnostics RNAscope RNA in situ hybridization assays for CLDN9

    (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 chordates.

    Orthologs for CLDN9 gene from Selected species (see all 8)    About this table
    Organism Taxonomic
    classification
    Gene Description Human
    Similarity
    Orthology
    Type
    Details
    mouse
    (Mus musculus)
    Mammalia Cldn91 , 5 claudin 91, 5 86.94(n)1
    97.24(a)1
      17 (11.99 cM)5
    568631  NM_020293.31  NP_064689.21 
     236825845 
    lizard
    (Anolis carolinensis)
    Reptilia --
    Uncharacterized protein
    64(a)
    1 → many
    GL343287.1(1328263-1328919)
    zebrafish
    (Danio rerio)
    Actinopterygii cldnc1 claudin c 62.37(n)
    62.21(a)
      81582  NM_131764.1  NP_571839.1 


    ENSEMBL Gene Tree for CLDN9 (if available)
    TreeFam Gene Tree for CLDN9 (if available)

    (Paralogs according to 1HomoloGene,
    2Ensembl, and 3SIMAP, Pseudogenes according to 4Pseudogene.org Build 68)
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    Paralogs for CLDN9 gene
    CLDN42  CLDN82  CLDN202  CLDN172  CLDN52  CLDN22  CLDN12  CLDN142  
    CLDN32  CLDN62  CLDN72  CLDN192  
    Selected SIMAP similar genes for CLDN9 using alignment to 1 protein entry:     CLD9_HUMAN(see all similar genes):
    CLDN4    CLDN6    CLDN3    CLDN7    CLDN5    CLDN8
    CLDN2    CLDN1    CLDN17    CLDN19    CLDN14    CLDN18
    CLDN10    CLDN20    CLDN22    CLDN24    CLDN15    CLDN25

    Find genes that share paralogs with CLDN9           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 CLDN9 (see all 158)    About this table                                 

    Genomic DataTranscription Related DataAllele Frequencies
    SNP IDValidClinical
    significance
    Chr 16 posSequence#AA
    Chg
    TypeMore#Allele
    freq
    PopTotal
    sample
    More
    ----------
    rs800215031,2
    C--3060483(+) ATGGAG/TTGCGG 1 -- us2k10--------
    rs1878680991,2
    --3060514(+) GCAGAC/TTCTAA 1 -- us2k10--------
    rs20239131,2
    C,F,A,H--3060543(-) GAGGTA/GGGAGG 1 -- us2k14Minor allele frequency- G:0.39NA WA CSA EA 126
    rs571561781,2
    F--3060608(+) TGTGTA/GTATAT 1 -- us2k11Minor allele frequency- G:0.11WA 118
    rs2006355051,2
    --3060620(+) ATATA-/TTATAT 1 -- us2k10--------
    rs2012539611,2
    --3060622(+) ATATA-/TTATTT 1 -- us2k10--------
    rs585098491,2
    C--3060624(+) TATAT-/A/AT  
            
    TTTTT
    1 -- us2k10--------
    rs1484247131,2
    C--3060624(+) ATATA-/TTTTTT 1 -- us2k10--------
    rs341184241,2
    C--3060625(+) TATAT-/A/TTTTTT 1 -- us2k10--------
    rs15485391,2
    --3060626(-) aaaaaA/Tatata 1 -- us2k11Minor allele frequency- T:0.00NA 2

    HapMap Linkage Disequilibrium report for CLDN9 (3062457 - 3064506 bp)

    Structural Variations
         Database of Genomic Variants (DGV) Selected variations for CLDN9 (see all 11):    About this table    
    Variant IDTypeSubtypePubMed ID
    nsv509588CNV Insertion20534489
    dgv2579n71CNV Loss21882294
    nsv510673CNV Loss20534489
    nsv905193CNV Loss21882294
    nsv905170CNV Loss21882294
    nsv905185CNV Loss21882294
    dgv2575n71CNV Loss21882294
    dgv2576n71CNV Loss21882294
    dgv2577n71CNV Loss21882294
    dgv2578n71CNV Loss21882294

    Site Specific Mutation Identification with PCR Assays
    SeqTarget long-range PCR primers for resequencing CLDN9
    DNA2.0 Custom Variant and Variant Library Synthesis for CLDN9

    (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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    5 diseases for CLDN9:    
    About MalaCards
    endolymphatic hydrops    gastric adenocarcinoma    hepatitis c virus    hepatitis c
    hepatitis

    1 disease from the University of Copenhagen DISEASES database for CLDN9:
    Endolymphatic hydrops

    Find genes that share disorders with CLDN9           About GenesLikeMe

    Genetic Association Database (GAD): CLDN9
    Human Genome Epidemiology (HuGE) Navigator: CLDN9 (1 document)

    Export disorders for CLDN9 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 CLDN9 gene, integrated from 10 sources (see all 24):
    (articles sorted by number of sources associating them with CLDN9)
        Utopia: connect your pdf to the dynamic
    world of online information

    1. Association between genetic variants in VEGF, ERCC3 and occupational benzene haematotoxicity. (PubMed id 19773279)1, 4 Hosgood H.D....Lan Q. (Occup Environ Med 2009)
    2. The tight junction proteins claudin-1, -6, and -9 are entry cofactors for hepatitis C virus. (PubMed id 18234789)1, 3 Meertens L....Dragic T. (J. Virol. 2008)
    3. 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)
    4. Analysis of a human gene homologous to rat ventral prostate.1 protein. (PubMed id 9441748)1, 3 Peacock R.E.... Inglehearn C.F. (Genomics 1997)
    5. Functional analysis of claudin-6 and claudin-9 as entry factors for hepatitis C virus infection of human hepatocytes by using monoclonal antibodies. (PubMed id 23864633)1 Fofana I....Baumert T.F. (J. Virol. 2013)
    6. Claudin-6, 7, or 9 overexpression in the human gastric adenocarcinoma cell line AGS increases its invasiveness, migration, and proliferation rate. (PubMed id 20874001)1 Zavala-Zendejas V.E....Rendon-Huerta E.P. (Cancer Invest. 2011)
    7. Distribution and expression pattern of claudins 6, 7, and 9 in diffuse- and intestinal-type gastric adenocarcinomas. (PubMed id 19960275)1 RendA^n-Huerta E....MontaA+o L.F. (J Gastrointest Cancer 2010)
    8. A claudin-9-based ion permeability barrier is essential for hearing. (PubMed id 19696885)1 Nakano Y....BA!nfi B. (PLoS Genet. 2009)
    9. The claudins. (PubMed id 19706201)1 Lal-Nag M. and Morin P.J. (Genome Biol. 2009)
    10. Structure and function of claudins. (PubMed id 18036336)1 Krause G....Blasig I.E. (Biochim. Biophys. Acta 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)
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    Entrez Gene: 9080 HGNC: 2051 AceView: CLDN9 Ensembl:ENSG00000213937 euGenes: HUgn9080
    ECgene: CLDN9 Kegg: 9080 H-InvDB: CLDN9

    (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 CLDN9 Pharmacogenomics, SNPs, Pathways
    ATLAS Chromosomes in Cancer entry for CLDN9 Genetics and Cytogenetics in Oncology and Haematology

    (Patent information from GeneIP,
    Licensable technologies from WIS Yeda, Salk, Tufts,
    IP news from LifeMap Sciences, Inc.)
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    Patent Information for CLDN9 gene:
    Search GeneIP for patents involving CLDN9

    GeneCards and IP:
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