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

CLDN9 Gene

protein-coding   GIFtS: 54
GCID: GC16P003062

Claudin 9

  See 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)
About This Section

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, Tocris Bioscience, Wikipedia's Gene Wiki, PharmGKB,
UniProtKB/Swiss-Prot, and/or UniProtKB/TrEMBL)
About This Section

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 gastric adenocarcinoma, and endolymphatic hydrops, and among its related super-pathways are Cell-cell junction organization and Sertoli-Sertoli Cell Junction Dynamics. 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 73), Regulatory elements and Epigenetics data according to QIAGEN, SABiosciences, and/or SwitchGear Genomics)
About This Section
RefSeq DNA sequence:
NC_000016.9  NC_018927.2  NT_010393.16  
Regulatory elements:
   SABiosciences 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 SABiosciences Chromatin IP Primers for CLDN9

Epigenetics:
QIAGEN PyroMark CpG Assay predesigned Pyrosequencing DNA Methylation assays 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 UniProtKB, HORDE, neXtProt, Ensembl, and/or Reactome, Modification sites according to PhosphoSitePlus, Specific Peptides from DME, Protein expression images according to data from SPIRE 1MOPED, 2PaxDb, and 3MAXQB 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 Cloud-Clone Corp.,
Biochemical Assays by EMD Millipore, R&D Systems, OriGene, GenScript, Cell Signaling Technology, Enzo Life Sciences, and/or Cloud-Clone Corp., Ontologies according to Gene Ontology Consortium 01 Oct 2013 and Entrez Gene, Antibodies by EMD Millipore, R&D Systems, GenScript, Cell Signaling Technology, OriGene, Novus Biologicals, Thermo Fisher Scientific, LSBio, Abcam, and/or Cloud-Clone Corp.)
About This Section

UniProtKB/Swiss-Prot: CLD9_HUMAN, O95484 (See protein sequence)
Recommended Name: Claudin-9  
Size: 217 amino acids; 22848 Da
Subcellular location: Cell junction, tight junction. Cell membrane; Multi-pass membrane protein

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

Post-translational modifications:

  • View modification sites using PhosphoSitePlus
  • View neXtProt modification sites for NX_O95484

  • CLDN9 Protein expression data from MOPED1, PaxDb2 and MAXQB3 : --
    REFSEQ proteins: NP_066192.1  
    ENSEMBL proteins: 
     ENSP00000398017  
    Reactome Protein details: O95484
    Human Recombinant Protein Products for CLDN9: 
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    Cloud-Clone Corp. Proteins for CLDN9 

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

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

    CLDN9 for ontologies           About GeneDecksing



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    Cloud-Clone Corp. CLIAs for CLDN9


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


    CLDN9 for domains           About GeneDecksing


    (According to 1UniProtKB, Genatlas, LifeMap Discovery™, IUBMB, and/or 2DME, Human phenotypes from GenomeRNAi, Animal models from MGI Mar 06 2013, inGenious Targeting Laboratory, genOway,
    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, Sirion Biotech, Clones from EMD Millipore, OriGene, SwitchGear Genomics, GenScript, Sino Biological, DNA2.0, Vector BioLabs, and Sirion Biotech, Cell Lines from GenScript, LifeMap BioReagents, In Situ Hybridization Assays from Advanced Cell Diagnostics, Ontologies according to Gene Ontology Consortium 01 Oct 2013 via Entrez Gene.)
    About This Section

    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 (GO ID links to tree view):    About this table

    GO IDQualified GO termEvidencePubMed IDs
    GO:0005198structural molecule activity IEA--
    GO:0042802identical protein binding ISS--
         
    CLDN9 for ontologies           About GeneDecksing


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

    CLDN9 for phenotypes           About GeneDecksing

    Animal Models:
       inGenious Targeting Laboratory - Custom generated mouse model solutions for CLDN9 
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       genOway customized KO model: permanent, tissue-specific or time-controlled inactivation for CLDN9 
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    miRNA
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    Inhib. RNA
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    Advanced Cell Diagnostics RNAscope RNA in situ hybridization assays for CLDN9


    (Pathways according to EMD Millipore, 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 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 Oct 2013 via Entrez Gene).
    About This Section

    SuperPaths for CLDN9 About   (see all 7)                                                                                              See pathways by source

    SuperPathContained pathways About
    1Cell-cell junction organization
    Cell-cell junction organization0.69
    Cell-Cell communication0.64
    Cell junction organization0.69
    Tight junction interactions0.49
    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

    Pathways by source                                                                                                                                                                 See SuperPaths
    Show all pathways

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

    4        Reactome Pathways for CLDN9
        Tight junction interactions
    Cell junction organization
    Cell-Cell communication
    Cell-cell junction organization


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


    CLDN9 for pathways           About GeneDecksing

    Interactions:

        Search SABiosciences Gene Network CentralTM Interacting Genes and Proteins Networks for CLDN9

    Gene Ontology (GO): 4 biological process terms (GO ID links to tree view):    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--

    CLDN9 for ontologies           About GeneDecksing



    (Chemical Compounds according to UniProtKB, Enzo Life Sciences, EMD Millipore, Tocris Bioscience HMDB, BitterDB, and/or Novoseek, Ligands according to IUPHAR, 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 CLDN9 (CLD9)

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

    Search CenterWatch for drugs/clinical trials and news about CLDN9 / CLD9

    (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,
    Conferences by KenesGroup, 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, Sirion Biotech, Primers from OriGene, SABiosciences, and/or QIAGEN )
    About This Section

    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 QIAGEN miScript miRNA Assays for microRNA that regulate CLDN9:
    hsa-miR-105
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    Inhib. RNA
    Products:
         
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                         Customized lentivirus expression plasmids for stable overexpression of CLDN9 
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    OriGene qPCR primer pairs and template standards for CLDN9
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      QIAGEN 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™, 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

    CLDN9 expression in normal human tissues (normalized intensities)      CLDN9 embryonic expression: see
    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 
     5/3 selected tissues (see all 3) fully expand
     
     Nose (Sensory Organs)
             sensory organ/nose/nasal cavity   
     
     Bone (Muscoskeletal System)
             Zeugopod Epiphyseal End
     
     Head Mesenchyme (Muscoskeletal System)
             Frontonasal Process

    Genevestigator expression for CLDN9

    SOURCE GeneReport for Unigene cluster: Hs.296949
        SABiosciences Expression via Pathway-Focused 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)
    About This Section

    This gene was present in the common ancestor of chordates.

    Orthologs for CLDN9 gene from 4/9 species (see all 9)    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 
    chicken
    (Gallus gallus)
    Aves LOC4174741 claudin-3-like 69.31(n)
    61.21(a)
      417474  XM_003642385.1  XP_003642433.1 
    lizard
    (Anolis carolinensis)
    Reptilia --
    Uncharacterized protein
    66(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)
    About This Section
    Paralogs for CLDN9 gene
    CLDN42  CLDN82  CLDN202  CLDN172  CLDN52  CLDN102  CLDN22  CLDN152  
    CLDN12  CLDN32  CLDN142  CLDN62  CLDN72  CLDN192  
    18/19 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

    CLDN9 for paralogs           About GeneDecksing



    (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) 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

    10/158 SNPs in CLDN9 are shown (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) 10/11 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

    SABiosciences Cancer Mutation PCR Assays
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    (in which this Gene is Involved, According to MalaCards, OMIM, UniProtKB, the University of Copenhagen DISEASES database, Conferences by KenesGroup, Genatlas, GeneTests, GAD, HuGE Navigator, and/or TGDB.)
    About This Section
    8 diseases for CLDN9:    About MalaCards
    gastric adenocarcinoma    endolymphatic hydrops    hepatitis c    hepatitis
    endotheliitis    gastric cancer    adenocarcinoma    prostatitis

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

    CLDN9 for disorders           About GeneDecksing

    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)
    About This Section

    PubMed articles for CLDN9 gene, integrated from 9 sources (see all 23):
    (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 a nd occupational benzene haematotoxicity. (PubMed id 19773279)1, 4 Hosgood H.D....Lan Q. (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. (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. (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. (1997)
    5. Claudin-6, 7, or 9 overexpression in the human gastri c adenocarcinoma cell line AGS increases its invasiveness, migration, and proli feration rate. (PubMed id 20874001)1 Zavala-Zendejas V.E....Rendon-Huerta E.P. (2011)
    6. 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. (2010)
    7. A claudin-9-based ion permeability barrier is essenti al for hearing. (PubMed id 19696885)1 Nakano Y....BA!nfi B. (2009)
    8. The claudins. (PubMed id 19706201)1 Lal-Nag M. and Morin P.J. (2009)
    9. Structure and function of claudins. (PubMed id 18036336)1 Krause G....Blasig I.E. (2008)
    10. Claudin-6 and claudin-9 function as additional coreceptors for hepatitis C virus. (PubMed id 17804490)1 Zheng A....Deng H. (2007)

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    (According to Entrez Gene, HGNC, AceView, euGenes, Ensembl, miRBase, ECgene, Kegg, and/or H-InvDB)
    About This Section
    Entrez Gene: 9080 HGNC: 2051 AceView: CLDN9 Ensembl:ENSG00000213937 euGenes: HUgn9080
    ECgene: CLDN9 Kegg: 9080 H-InvDB: CLDN9

    (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 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.)
    About This Section
    Patent Information for CLDN9 gene:
    Search GeneIP for patents involving CLDN9

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



    (Antibodies, recombinant proteins, and assays from EMD Millipore, R&D Systems, OriGene, QIAGEN, GenScript, Cell Signaling Technology, SABiosciences, Novus Biologicals, Sino Biological, Enzo Life Sciences, Abcam, ProSpec, Cloud-Clone Corp., Thermo Fisher Scientific, LSBio, Gene Editing from DNA2.0 and Sirion Biotech, Clones from EMD Millipore, OriGene, GenScript, Sino Biological, DNA2.0, SwitchGear Genomics, Vector BioLabs, Sirion Biotech, Cell lines from GenScript, and LifeMap BioReagents, PCR Arrays from SABiosciences, Drugs and/or compounds from EMD Millipore, Tocris Bioscience, and/or Enzo Life Sciences, In Situ Hybridization Assays from
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    GeneCards Homepage - Last full update: 23 Oct 2013 - Incrementals: 3 Nov 2013 , 7 Nov 2013 , 23 Jan 2014

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