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

SLC26A9 Gene

protein-coding   GIFtS: 55
GCID: GC01M205883

solute carrier family 26, member 9

 Explore 13 diseases affiliated with
SLC26A9 via our new
 Human Malady Compendium 
Biological research products
for SLC26A9
    

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

Aliases
Solute Carrier Family 26, Member 91 2
Anion Transporter/Exchanger Protein 92 3
Anion Transporter/Exchanger-92
Solute Carrier Family 26 Member 92

External Ids:    HGNC: 144691   Entrez Gene: 1150192   Ensembl: ENSG000001745027   OMIM: 6084815   UniProtKB: Q7LBE33   

Export aliases for SLC26A9 gene to outside databases

Previous GC identifers: GC01M203885 GC01M201419 GC01M202243 GC01M203060 GC01M202613 GC01M204148 GC01M177045


(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 SLC26A9:
This gene is one member of a family of sulfate/anion transporter genes. Family members are well conserved in their
genomic (number and size of exons) and protein (aa length among species) structures yet have markedly different tissue
expression patterns. The product of this gene is a highly selective chloride ion channel regulated by WNK kinases.
Alternative splicing results in multiple transcript variants encoding differing isoforms.(provided by RefSeq, Dec
2008)

UniProtKB/Swiss-Prot: S26A9_HUMAN, Q7LBE3
Function: DIDS- and thiosulfate- sensitive anion exchanger mediating chloride, sulfate and oxalate transport. Mediates
chloride/bicarbonate exchange or chloride-independent bicarbonate extrusion thus assuring bicarbonate secretion.
Inhibited by ammonium and thiosulfate




(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_004487.19  
Regulatory elements:
   SABiosciences Regulatory transcription factor binding sites in the SLC26A9 gene promoter:
         MZF-1   Spz1   NF-1/L   NF-1   GATA-3   HTF   FOXD3   Cdc5   
         Other transcription factors

SwitchGear Promoter luciferase reporter plasmidSLC26A9 promoter sequence
   Search SABiosciences Chromatin IP Primers for SLC26A9

Epigenetics:
QIAGEN PyroMark CpG Assay predesigned Pyrosequencing DNA Methylation assays in human, mouse, rat SLC26A9


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

Entrez Gene cytogenetic band: 1q32.1   Ensembl cytogenetic band:  1q32.1   HGNC cytogenetic band: 1q32.1

SLC26A9 Gene in genomic location: bands according to Ensembl, locations according to (and/or Entrez Gene and/or Ensembl if different)
SLC26A9 gene location

GeneLoc information about chromosome 1         GeneLoc Exon Structure

GeneLoc location for GC01M205883:  view genomic region     (about GC identifiers)

Start:
205,882,176 bp from pter      End:
205,912,588 bp from pter
Size:
30,413 bases      Orientation:
minus strand

(According to 1UniProtKB, HORDE, neXtProt, Ensembl, and/or Reactome, Modification sites according to 2PhosphoSitePlus, Specific Peptides from DME, Protein expression images according to data from SPIRE MOPED and PaxDb, RefSeq according to NCBI, PDB rendering according to OCA and/or Proteopedia, Recombinant Proteins from EMD Millipore, R&D Systems, GenScript, Enzo Life Sciences, OriGene, Novus Biologicals, Sino Biological, ProSpec, and/or Uscn,
Biochemical Assays by EMD Millipore, R&D Systems, OriGene, GenScript, Cell Signaling Technology, Enzo Life Sciences, and/or Uscn, Ontologies according to Gene Ontology Consortium 01 Mar 2013 and Entrez Gene, Antibodies by EMD Millipore, R&D Systems, GenScript, Cell Signaling Technology, OriGene, Novus Biologicals, Thermo Fisher Scientific, Abcam, and/or Uscn)
About This Section

UniProtKB/Swiss-Prot: S26A9_HUMAN, Q7LBE3 (See protein sequence)
Recommended Name: Solute carrier family 26 member 9  
Size: 791 amino acids; 86988 Da
Subcellular location: Membrane; Multi-pass membrane protein (Potential)
Sequence caution: Sequence=AAL26867.1; Type=Erroneous termination; Positions=792; Note=Translated as stop;
Sequence=EAW91587.1; Type=Erroneous termination; Positions=792; Note=Translated as stop;
Secondary accessions: A7E2V6 B1AVM9 B7ZKK2 Q96PK9 Q96RN0

Explore the universe of human proteins at neXtProt for SLC26A9: NX_Q7LBE3

Post-translational modifications:

  • View modification sites using PhosphoSitePlus2
  • View neXtProt modification sites for NX_Q7LBE3

  • SLC26A9 Protein expression data from MOPED and PaxDb:    About this image 
    SLC26A9 Protein Expression
    REFSEQ proteins (2 alternative transcripts): 
    NP_443166.1  NP_599152.2  

    ENSEMBL proteins: 
     ENSP00000341682   ENSP00000356103   ENSP00000356102  
    Reactome Protein details: Q7LBE3
    Human Recombinant Protein Products for SLC26A9: 
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    Uscn Proteins for SLC26A9

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

    GO IDQualified GO termEvidencePubMed IDs
    GO:0005886plasma membrane TAS--
    GO:0016021integral to membrane IEA--
    GO:0016324apical plasma membrane ----

    SLC26A9 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

    SLC26A9 for domains           About GeneDecksing

    3 InterPro domains/families:
     IPR002645 STAS_dom
     IPR001902 SulP_transpt
     IPR011547 Sulph_transpt

    Graphical View of Domain Structure for InterPro Entry Q7LBE3

    ProtoNet protein and cluster: Q7LBE3

    1 Blocks protein family: IPB001902 Sulphate transporter

    UniProtKB/Swiss-Prot: S26A9_HUMAN, Q7LBE3
    Similarity: Belongs to the SLC26A/SulP transporter (TC 2.A.53) family
    Similarity: Contains 1 STAS domain


    (According to 1UniProtKB, Genatlas, LifeMap Discovery™, IUBMB, and/or 2DME, Human phenotypes from GenomeRNAi, Animal models from MGI Mar 06 2013, inGenious Targeting Laboratory,
    bound targets from SABiosciences, miRNA Gene Targets from miRTarBase, shRNA from OriGene, Sirion Biotech, 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, and Vector BioLabs, Cell Lines from GenScript, LifeMap BioReagents, Sirion Biotech, In Situ Hybridization Assays from Advanced Cell Diagnostics, Ontologies according to Gene Ontology Consortium 01 Mar 2013 via Entrez Gene.)
    About This Section

    Molecular Function:

         UniProtKB/Swiss-Prot Summary: S26A9_HUMAN, Q7LBE3
    Function: DIDS- and thiosulfate- sensitive anion exchanger mediating chloride, sulfate and oxalate transport. Mediates
    chloride/bicarbonate exchange or chloride-independent bicarbonate extrusion thus assuring bicarbonate secretion.
    Inhibited by ammonium and thiosulfate

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

    GO IDQualified GO termEvidencePubMed IDs
    GO:0008271secondary active sulfate transmembrane transporter activity IEA--
    GO:0015106bicarbonate transmembrane transporter activity ----
    GO:0015301anion:anion antiporter activity ----
         
    SLC26A9 for ontologies           About GeneDecksing


    Phenotypes:
         1 MGI mutant phenotype (inferred from 1 allele(MGI details for Slc26a9):
     digestive/alimentary 

    SLC26A9 for phenotypes           About GeneDecksing

    Animal Models:
         Mouse knock-out Slc26a9tm1Sole for SLC26A9
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    (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
    1SLC-mediated transmembrane transport
    SLC-mediated transmembrane transport1.00
    Transmembrane transport of small molecules0.50
    2Multifunctional anion exchangers
    Multifunctional anion exchangers1.00
    3Mineral absorption
    Mineral absorption1.00
    4Amino acid and oligopeptide SLC transporters
    Transport of inorganic cations/anions and amino acids/oligopeptides0.52

    Pathway sources
    See GeneCards unified pathways
    Show all pathways


    4        Reactome Pathways for SLC26A9
        Multifunctional anion exchangers
    SLC-mediated transmembrane transport
    Transmembrane transport of small molecules
    Transport of inorganic cations/anions and amino acids/oligopeptides


    1         Kegg Pathway  (Kegg details for SLC26A9):
        Mineral absorption


    SLC26A9 for pathways           About GeneDecksing

    Interactions:

        Search SABiosciences Gene Network CentralTM Interacting Genes and Proteins Networks for SLC26A9

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

    5/6 Interacting proteins for SLC26A9 (Q7LBE33 ENSP000003416824) via UniProtKB, MINT, STRING, and/or I2D (see all 6)
    InteractantInteraction Details
    GeneCardExternal ID(s)
    CFTRP135693I2D: score=1 
    GCSAMENSP000003094874STRING: ENSP00000309487
    KIF21BENSP000003284944STRING: ENSP00000328494
    --ENSP000004062194STRING: ENSP00000406219
    --ENSP000004056544STRING: ENSP00000405654
    About this table

    Gene Ontology (GO): 5/6 biological process terms (GO ID links to tree view) (see all 6):    About this table

    GO IDQualified GO termEvidencePubMed IDs
    GO:0006811ion transport TAS--
    GO:0006821chloride transport ----
    GO:0006885regulation of pH ----
    GO:0008272sulfate transport IEA--
    GO:0015701bicarbonate transport ----

    SLC26A9 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 SLC26A9

    2 HMDB Compounds for SLC26A9    About this table
    CompoundSynonyms CAS #PubMed Ids
    ChlorineCl2 (see all 13)16887-00-6--
    Hydrogen carbonateBicarbonate (see all 19)71-52-3--
    Search CenterWatch for drugs/clinical trials and news about SLC26A9 / S26A9 

    (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, Sirion Biotech, 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 SLC26A9 gene (3 alternative transcripts): 
    NM_052934.3  NM_134325.2  NM_001142600.1  

    Unigene Cluster for SLC26A9:

    Solute carrier family 26, member 9
    Hs.164073  [show with all ESTs]
    Unigene Representative Sequence: AF331525
    6 Ensembl transcripts including schematic representations, and UCSC links where relevant:
    ENST00000340781 ENST00000367135(uc001hdm.3 uc001hdn.3 uc001hdp.3 uc001hdq.3)
    ENST00000491127(uc001hdo.3) ENST00000461505 ENST00000469392 ENST00000367134


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    Additional cDNA sequence: 

    AF314958.1 AF331525.1 AK091876.1 AK127491.1 BC037978.1 BC136538.1 BC144233.1 BC151208.1 

    3 DOTS entries:

    DT.40267422  DT.100688261  DT.97821000 

    24 AceView cDNA sequences:

    NM_052934 AX747232 AA862421 BI869085 NM_134325 BC037978 AF331525 AK127491 
    AK091876 BU158718 CB958492 AW192778 AW514334 AF314958 BI832996 AI432108 
    BX484774 BQ896842 AJ708138 BQ961349 BX484746 AI828448 CD636350 AI932662 

    GeneLoc Exon Structure

    5/6 Alternative Splicing Database (ASD) splice patterns (SP) for SLC26A9 (see all 6)    About this scheme

    ExUns: 1 ^ 2a · 2b ^ 3 ^ 4 ^ 5 ^ 6a · 6b ^ 7 ^ 8 ^ 9a · 9b ^ 10 ^ 11 ^ 12 ^ 13 ^ 14 ^ 15 ^ 16 ^ 17 ^ 18a · 18b ^ 19 ^ 20 ^ 21 ^ 22a ·
    SP1:                                      -                       -                                                           -                 -               
    SP2:                                      -                       -                                                           -                 -               
    SP3:                                                                                                                          -                 -               
    SP4:                                                                                                                                                            
    SP5:                                                                                                                                      -     -               

    ExUns: 22b ^ 23
    SP1:  -         
    SP2:            
    SP3:            
    SP4:            
    SP5:            


    ECgene alternative splicing isoforms for SLC26A9

    (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

    SLC26A9 expression in normal human tissues (normalized intensities)
    See probesets specificity/sensitivity at GeneAnnot
    About this imageBioGPS
    CGAP TAG: AGGCAGAGGG
    SLC26A9 Expression
    About this image
    See SLC26A9 Protein Expression from SPIRE MOPED and PaxDB
    Genevestigator expression for SLC26A9

    SOURCE GeneReport for Unigene cluster: Hs.164073

    UniProtKB/Swiss-Prot: S26A9_HUMAN, Q7LBE3
    Tissue specificity: Predominantly expressed in lung at the luminal side of the bronchiolar and alveolar epithelium of
    lung. To a lower extent, also expressed in pancreas and prostate

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    In Situ
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    (Orthologs according to 1,2HomoloGene (2older version, for species not in 1newer version), 3euGenes, 4SGD , 5MGI Mar 06 2013, with possible further links to Flybase and/or WormBase, and/or 6Ensembl pan taxonomic compara , Gene Trees according to Ensembl and TreeFam)
    About This Section

    This gene was present in the common ancestor of animals.

    Orthologs for SLC26A9 gene from 4/18 species (see all 18)    About this table
    Organism Taxonomic
    classification
    Gene Description Human
    Similarity
    Orthology
    Type
    Details
    chicken
    (Gallus gallus)
    Aves SLC26A91 solute carrier family 26, member 9 71.13(n)
    72.19(a)
      428262  XM_425821.2  XP_425821.2 
    lizard
    (Anolis carolinensis)
    Reptilia SLC26A96
    --
    66(a)
    1 ↔ 1
    GL343228.1(793354-837614)
    fruit fly
    (Drosophila melanogaster)
    Insecta Prestin6
    Prestin
    25(a)
    possible ortholog
    3L(17891989-17900912)
    worm
    (Caenorhabditis elegans)
    Secernentea W04G3.63 dra like protein 33(a)
    (best of 2)
      X(11115908-11117663)   --


    ENSEMBL Gene Tree for SLC26A9 (if available)
    TreeFam Gene Tree for SLC26A9 (if available) 

    (Paralogs according to 1HomoloGene,
    2Ensembl, and 3SIMAP, Pseudogenes according to 4Pseudogene.org Build 68)
    About This Section
    Paralogs for SLC26A9 gene
    SLC26A32  SLC26A62  SLC26A12  SLC26A52  SLC26A22  SLC26A112  SLC26A102  SLC26A72  
    SLC26A42  SLC26A82  
    12 SIMAP similar genes for SLC26A9 using alignment to 2 protein entries:     S26A9_HUMAN (see all proteins):
    DKFZp686P10213    RESDA1    SLC26A4    SLC26A5    SLC26A6    PRES
    SLC26A3    SLC26A10    SLC26A7    SLC26A2    SLC26A1    SLC26A8

    SLC26A9 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

    10/742 NCBI SNPs in SLC26A9 are shown (see all 742    About this table
    Genomic DataTranscription Related DataAllele Frequencies
    SNP IDValidClinical
    significance
    Chr 1 posSequence#AA
    Chg
    TypeMore#Allele
    freq
    PopTotal
    sample
    More
    ----------
    rs1824086241,2
    --205881753(+) CTCACA/GAACAG 2 -- ds50010--------
    rs1866856431,2
    --205881820(+) TTTGCA/TAAGTA 2 -- ds50010--------
    rs22824291,2
    C,F,O,H--205881824(+) CTAAGT/CAACGA 2 -- ds500123Minor allele frequency- C:0.28EA NA NS WA 4044
    rs1474776831,2
    --205881827(+) AGTAAC/TGATGG 2 -- ds50010--------
    rs1925732411,2
    --205881829(+) TAACGA/GTGGGA 2 -- ds50010--------
    rs115833961,2
    H--205881995(+) CTTTAG/ACTGGA 2 -- ds50014Minor allele frequency- A:0.00NS EA 420
    rs1151724551,2
    C,F--205882035(+) AAAATC/GGAACC 2 -- ds50011Minor allele frequency- G:0.03WA 118
    rs1832543961,2
    --205882073(+) AAATCA/TGAGTC 2 -- ds50010--------
    rs1890353331,2
    --205882093(+) TCCCCC/TGCCCG 2 -- ds50010--------
    rs1929799601,2
    --205882164(+) CCACCC/GAAACA 2 -- ds50010--------

    HapMap Linkage Disequilibrium report for SLC26A9 (205882176 - 205912588 bp)
    Structural Variations (Copy Number Variations, Insertions/Deletions, Inversions)
    Database of Genomic Variants (DGV): 1 variation for SLC26A9
         1 CNV: 71031
    Human Gene Mutation Database (HGMD): SLC26A9

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    (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

    SLC26A9 for disorders           About GeneDecksing

    OMIM gene information: 608481    OMIM disorders: --

    13 diseases for SLC26A9:    About MalaCards
    diastrophic dysplasia    cystic fibrosis    fainting    hepatitis c
    pharyngitis    hepatitis    fibrosis    schizophrenia
    tuberculosis    malaria    prostatitis    neuronitis
    mycobacterium tuberculosis

    1 disease from the University of Copenhagen DISEASES database for SLC26A9:
    Diastrophic dysplasia
    Human Genome Epidemiology (HuGE) Navigator: SLC26A9 (2 documents)

    Export disorders for SLC26A9 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 SLC26A9 gene, integrated from 9 sources (see all 21):
    (articles sorted by number of sources associating them with SLC26A9)
        Utopia: connect your pdf to the dynamic
    world of online information

    1. Functional characterization of three novel tissue-specific anion exchangers SLC26A7, -A8, and -A9. (PubMed id 11834742)1, 2, 3 Lohi H.... Kere J. (2002)
    2. Functional analysis of nonsynonymous single nucleotide polymorphisms in human SLC26A9. (PubMed id 22544634)1, 2 Chen A.P.... Romero M.F. (2012)
    3. SLC26A9-mediated chloride secretion prevents mucus obs truction in airway inflammation. (PubMed id 22945630)1 Anagnostopoulou P....Mall M.A. (2012)
    4. Differential contribution of SLC26A9 to Cl(-) conducta nce in polarized and non-polarized epithelial cells. (PubMed id 21809345)1 Ousingsawat J....Kunzelmann K. (2012)
    5. Multiple apical plasma membrane constituents are assoc iated with susceptibility to meconium ileus in individuals with cystic fibrosis. (PubMed id 22466613)1 Sun L....Strug L.J. (2012)
    6. Characterization of the L683P mutation of SLC26A9 in Xenopus oocytes. (PubMed id 21439353)1 Avella M....Ehrenfeld J. (2011)
    7. Genome-wide pharmacogenomic study of neurocognition a s an indicator of antipsychotic treatment response in schizophrenia. (PubMed id 21107309)1 McClay J.L....van den Oord E.J. (2011)
    8. SLC26A9 stimulates CFTR expression and function in hu man bronchial cell lines. (PubMed id 20658517)1 Avella M....Ehrenfeld J. (2011)
    9. Large-scale candidate gene analysis of spontaneous cl earance of hepatitis C virus. (PubMed id 20331378)1 Mosbruger T.L....Thio C.L. (2010)
    10. SLC26A9 is a constitutively active, CFTR-regulated anion conductance in human bronchial epithelia. (PubMed id 19289574)1 Bertrand C.A....Frizzell R.A. (2009)

    (in PubMed, OMIM, and NCBI Bookshelf)
    About This Section
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    (According to Entrez Gene, HGNC, AceView, euGenes, Ensembl, miRBase, ECgene, Kegg, and/or H-InvDB)
    About This Section
    Entrez Gene: 115019 HGNC: 14469 AceView: SLC26A9 Ensembl:ENSG00000174502 euGenes: HUgn115019
    ECgene: SLC26A9 Kegg: 115019 H-InvDB: SLC26A9

    (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 SLC26A9 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 SLC26A9 gene:
    Search GeneIP for patents involving SLC26A9

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



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