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

SLC26A7 Gene

protein-coding   GIFtS: 55
GCID: GC08P092221

solute carrier family 26, member 7
 Explore 14 diseases affiliated with
SLC26A7 via
MalaCards
our new
 Human Malady Compendium 
Biological research products
for SLC26A7    

Aliases
for SLC26A7 gene

(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 71 2
SUT21 2 3
Anion Exchange Transporter2
Sulfate Anion Transporter2
Solute Carrier Family 26 Member 73

External Ids:    HGNC: 144671   Entrez Gene: 1151112   Ensembl: ENSG000001476067   OMIM: 6084795   UniProtKB: Q8TE543   

Export aliases for SLC26A7 gene to outside databases

Previous GC identifers: GC08P090739 GC08P092107 GC08P091930 GC08P092218 GC08P092330 GC08P087472


Summaries
for SLC26A7 gene

(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 SLC26A7:
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. This gene has abundant and specific expression in the kidney. Splice variants that use both
alternate transcription initiation and polyadenylation sites have been described for this gene. (provided by RefSeq,
Jul 2008)

UniProtKB/Swiss-Prot: S26A7_HUMAN, Q8TE54
Function: Acts as a sodium-independent DIDS-sensitive anion exchanger mediating bicarbonate, chloride, sulfate and
oxalate transport. May play a role in the maintenance of the electrolyte and acid-base homeostasis in the kidney, by
acting as a distal excretory segment-specific anion exchanger. Plays a major role in gastric acid secretion

Gene Wiki entry for SLC26A7


Genomic Views
for SLC26A7 gene

(According to GeneLoc and/or HGNC, and/or
Entrez Gene (NCBI build 37),
and/or miRBase,
Genomic Views according to UCSC (hg19) and Ensembl (release 69), Regulatory elements and Epigenetics data according to QIAGEN, SABiosciences, and/or SwitchGear Genomics)
About This Section
RefSeq DNA sequence:
NC_000008.10  NC_018919.1  NT_008046.16  
Regulatory elements:
   SABiosciences Regulatory transcription factor binding sites in the SLC26A7 gene promoter:
         AML1a   Pbx1a   POU6F1 (c2)   STAT5A   Ik-3   Meis-1b   FOXL1   AREB6   HOXA5   Pax-4a   
         Other transcription factors

SwitchGear Promoter luciferase reporter plasmid: SLC26A7 promoter sequence
   Search SABiosciences Chromatin IP Primers for SLC26A7

Epigenetics:
QIAGEN PyroMark CpG Assay predesigned Pyrosequencing DNA Methylation assays in human, mouse, rat SLC26A7


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

Entrez Gene cytogenetic band: 8q23   Ensembl cytogenetic band:  8q21.3   HGNC cytogenetic band: 8q23

SLC26A7 Gene in genomic location: bands according to Ensembl, locations according to (and/or Entrez Gene and/or Ensembl if different)
SLC26A7 gene location

GeneLoc information about chromosome 8         GeneLoc Exon Structure

GeneLoc location for GC08P092221:  view genomic region     (about GC identifiers)

Start:
 92,221,722 bp from pter      End:
 92,410,378 bp from pter
Size:
 188,657 bases      Orientation:
 plus strand

Proteins
for SLC26A7 gene

(According to 1UniProtKB, HORDE, neXtProt, Ensembl, and/or Reactome, Modification sites according to 2PhosphoSitePlus, Specific Peptides from DME, Protein expression images according to data from SPIRE MOPED and PaxDb, RefSeq according to NCBI, PDB rendering according to OCA and/or Proteopedia, Recombinant Proteins from EMD Millipore, R&D Systems, GenScript, Enzo Life Sciences, OriGene, Novus Biologicals, Sino Biological, ProSpec, and/or Uscn,
Biochemical Assays by EMD Millipore, R&D Systems, OriGene, GenScript, Cell Signaling Technology, Enzo Life Sciences, and/or Uscn, Ontologies according to Gene Ontology Consortium 01 Mar 2013 and Entrez Gene, Antibodies by EMD Millipore, R&D Systems, GenScript, Cell Signaling Technology, OriGene, Novus Biologicals, Thermo Fisher Scientific, Abcam, and/or Uscn)
About This Section
UniProtKB/Swiss-Prot: S26A7_HUMAN, Q8TE54 (See protein sequence)
Recommended Name: Anion exchange transporter  
Size: 656 amino acids; 72213 Da
Subcellular location: Recycling endosome membrane; Multi-pass membrane protein. Note=Expressed in the cytoplasm in
recycling endosomes of medullary collecting duct cells and in acid-secreting gastric parietal cells. Targeted to the
basolateral membrane in hypertonicity and potassium depletion
Miscellaneous: Is active at both alkaline and acidic pH. Activity is inhibited by
4,4'-Di-isothiocyanatostilbene-2,2'-disulfonic acid (DIDS - an inhibitor of several anion channels and transporters)
Secondary accessions: Q24JS8 Q8TE53 Q96RN2
Alternative splicing: 2 isoforms:  Q8TE54-1   Q8TE54-2   

Explore the universe of human proteins at neXtProt for SLC26A7: NX_Q8TE54

Post-translational modifications:

  • View modification sites using PhosphoSitePlus2
  • View neXtProt modification sites for NX_Q8TE54

    • SLC26A7 Protein expression data from MOPED and PaxDb:    About this image 
    Estimated protein expression log10 (pmol).

    REFSEQ proteins (2 alternative transcripts): 
    NP_439897.1  NP_599028.1  

    ENSEMBL proteins: 
     ENSP00000427712   ENSP00000428881   ENSP00000428849   ENSP00000276609   ENSP00000309504  
     ENSP00000428747  
    Reactome Protein details: Q8TE54
    Human Recombinant Protein Products: 
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    Uscn Proteins for SLC26A7

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

    GO IDQualified GO termEvidencePubMed IDs
    GO:0005737cytoplasm IDA16524946
    GO:0005768endosome IDA16524946
    GO:0005886plasma membrane TAS--
    GO:0016021integral to membrane IEA--
    GO:0016323basolateral plasma membrane ISS--


    SLC26A7 for ontologies           About GeneDecksing



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    Uscn ELISAs and CLIAs for SLC26A7

    Protein Domains /
    Families
    for SLC26A7 gene

    (According to InterPro, ProtoNet, UniProtKB, and/or BLOCKS, Sets of similar genes according to GeneDecks)
    About This Section
    SLC26A7 for domains           About GeneDecksing

    2 InterPro domains/families:
     IPR002645 STAS_dom
     IPR011547 Sulph_transpt

    Graphical View of Domain Structure for InterPro Entry Q8TE54

    ProtoNet protein and cluster: Q8TE54

    1 Blocks protein family: IPB001902 Sulphate transporter

    UniProtKB/Swiss-Prot: S26A7_HUMAN, Q8TE54
    Similarity: Belongs to the SLC26A/SulP transporter (TC 2.A.53) family
    Similarity: Contains 1 STAS domain


    Function
    for SLC26A7 gene

    (According to 1UniProtKB, Genatlas, LifeMap Discovery™, IUBMB, and/or 2DME, Human phenotypes from GenomeRNAi, Animal models from MGI Mar 06 2013,
    bound targets from SABiosciences, miRNA Gene Targets from miRTarBase shRNA from OriGene, RNAi from EMD Millipore, siRNAs from OriGene, QIAGEN, microRNA from QIAGEN, Gene Editing from DNA2.0, Clones from EMD Millipore, OriGene, SwitchGear Genomics, GenScript, Sino Biological, DNA2.0, and Vector BioLabs, Cell Lines from GenScript, LifeMap BioReagents, In Situ Hybridization Assays from Advanced Cell Diagnostics, Ontologies according to Gene Ontology Consortium 01 Mar 2013 via Entrez Gene.)
    About This Section
    Function Summary:

         UniProtKB/Swiss-Prot: S26A7_HUMAN, Q8TE54
    Function: Acts as a sodium-independent DIDS-sensitive anion exchanger mediating bicarbonate, chloride, sulfate and
    oxalate transport. May play a role in the maintenance of the electrolyte and acid-base homeostasis in the kidney, by
    acting as a distal excretory segment-specific anion exchanger. Plays a major role in gastric acid secretion

    miRNA
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    hsa-miR-26a-2* hsa-miR-4307 hsa-miR-4328 hsa-miR-200a hsa-miR-141 hsa-miR-223 hsa-miR-186 hsa-miR-222*
    SwitchGear 3'UTR luciferase reporter plasmid: SLC26A7 3' UTR sequence
    Inhib. RNA
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    Gene Editing
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    Clone
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    In Situ Assay
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    Gene Ontology (GO): 5/6 molecular function terms (GO ID links to tree view) (see all 6):    About this table

    GO IDQualified GO termEvidencePubMed IDs
    GO:0005253anion channel activity ----
    GO:0005254chloride channel activity IDA1183472
    GO:0015106bicarbonate transmembrane transporter activity ISS12736153
    GO:0015116sulfate transmembrane transporter activity IDA1183472
    GO:0015301anion:anion antiporter activity IEA--


    SLC26A7 for ontologies           About GeneDecksing


    Animal Models:
         Mouse knock-out Slc26a7tm1Sole for SLC26A7
         3 MGI mutant phenotypes (inferred from 1 allele) (MGI details for Slc26a7):
     digestive/alimentary  homeostasis/metabolism  renal/urinary system 

    SLC26A7 for phenotypes           About GeneDecksing


    Pathways & Interactions
    for SLC26A7 gene

    (Pathways according to EMD Millipore, R&D Systems, Cell Signaling Technology, KEGG, PharmGKB, BioSystems, Reactome, Tocris Bioscience, GeneGo (Thomson Reuters), QIAGEN, and/or UniProtKB, Sets of similar genes according to GeneDecks, Interaction Networks according to SABiosciences, and/or STRING, Interactions according to 1UniProtKB, 2MINT, 3I2D, and/or 4STRING, with links to IntAct and Ensembl, Ontologies according to Gene Ontology Consortium 01 Mar 2013 via Entrez Gene).
    About This Section

    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
    3Gastric acid secretion
    		Gastric acid secretion1.00
    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 SLC26A7
        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 SLC26A7):
        Gastric acid secretion


    SLC26A7 for pathways           About GeneDecksing

    Interactions:

        Search SABiosciences Gene Network CentralTM Interacting Genes and Proteins Networks for SLC26A7

    STRING Interaction Network Preview (showing 1 interactants - click image to see more details)

    1 Interacting protein for SLC26A7 (ENSP000003095044) via UniProtKB, MINT, STRING, and/or I2D
    InteractantInteraction Details
    GeneCardExternal ID(s)
    SLC4A2ENSP000003114024STRING: ENSP00000311402
    About this table

    Gene Ontology (GO): 5/8 biological process terms (GO ID links to tree view) (see all 8):    About this table

    GO IDQualified GO termEvidencePubMed IDs
    GO:0001696gastric acid secretion IEA--
    GO:0006811ion transport TAS--
    GO:0006820anion transport ----
    GO:0006821chloride transport IDA1183472
    GO:0008272sulfate transport IDA1183472


    SLC26A7 for ontologies           About GeneDecksing



    Drugs & Compounds
    for SLC26A7 gene

    (Chemical Compounds according to UniProtKB, Enzo Life Sciences, EMD Millipore, Tocris Bioscience HMDB, BitterDB, and/or Novoseek, and Drugs according to DrugBank, Enzo Life Sciences, and/or PharmGKB, with drugs/clinical trials/news search links to CenterWatch)
    About This Section
    Browse Small Molecules at EMD Millipore
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    Browse Tocris compounds for SLC26A7

    3 HMDB Compounds for SLC26A7    About this table
    CompoundSynonyms CAS #PubMed Ids
    ChlorineCl2 (see all 13)16887-00-6--
    Hydrogen carbonateBicarbonate (see all 19)71-52-3--
    SodiumSodium (see all 2)7440-23-5--
    Search CenterWatch for drugs/clinical trials and news about SLC26A7 / S26A7 

    Transcripts
    for SLC26A7 gene

    (Secondary structures according to fRNAdb,
    GenBank/EMBL/DDBJ Accessions according to
    Unigene (Build 235 Homo sapiens; Mar 10 2013) or GenBank,
    RefSeq according to Entrez Gene,
    DOTS (version 10), and/or AceView, transcript ids from Ensembl with links to UCSC,
    exon structure from GeneLoc, alternative splicing isoforms according to ASD and/or ECgene,
    RNAi Products from EMD Millipore,
    siRNAs from OriGene, QIAGEN, shRNA from OriGene, microRNA from QIAGEN,
    Tagged/untagged cDNA clones from OriGene, SwitchGear Genomics, GenScript, DNA2.0, Vector BioLabs, Primers from OriGene, SABiosciences, and/or QIAGEN )
    About This Section
    REFSEQ mRNAs for SLC26A7 gene (2 alternative transcripts): 
    NM_052832.2  NM_134266.1  

    Unigene Cluster for SLC26A7:

    Solute carrier family 26, member 7
    Hs.354013  [show with all ESTs]
    Unigene Representative Sequence: NM_052832
    8 Ensembl transcripts including schematic representations, and UCSC links where relevant:
    ENST00000522181 ENST00000522862 ENST00000523719 ENST00000276609(uc003yex.3 uc003yey.3 uc003yfa.3)
    ENST00000309536(uc003yez.3) ENST00000520818 ENST00000520249 ENST00000517930


    miRNA
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    QIAGEN Custom miScript Target Protector blocks miRNA-binding site of human, mouse, rat SLC26A7
    8/56 QIAGEN miScript miRNA Assays for microRNAs that regulate SLC26A7 (see all 56):
    hsa-miR-26a-2* hsa-miR-4307 hsa-miR-4328 hsa-miR-200a hsa-miR-141 hsa-miR-223 hsa-miR-186 hsa-miR-222*
    SwitchGear 3'UTR luciferase reporter plasmid: SLC26A7 3' UTR sequence
    Inhib. RNA
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    OriGene 29mer shRNA kits in GFP-retroviral vector in human, mouse, rat for SLC26A7 (see all 7)
    OriGene shRNA RFP: SLC26A7
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    Clone
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    Primer
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    Additional cDNA sequence: 

    AF331521.1 AJ413228.1 AJ413229.2 AJ413230.1 AK122933.1 BC113866.1 BC114474.1 

    8 DOTS entries:

    DT.40206364  DT.75159609  DT.40250744  DT.99962126  DT.40106731  DT.99941677  DT.100735821  DT.100735822 

    24/138 AceView cDNA sequences (see all 138):

    AW276475 AA449912 AW182183 BM542164 BX281278 AW514714 BU618683 AA813899 
    AI343847 AK130865 AF331521 AW571925 AJ413230 BM975667 AA252475 AJ413229 
    NM_016023 BI712470 BX642399 NM_134266 AA449911 CA773890 BM726084 AA748163 

    GeneLoc Exon Structure


    Expression
    for SLC26A7 gene

    (RNA expression data according to H-InvDB, NONCODE, miRBase, and RNAdb, Expression images according to data from BioGPS, Illumina Human BodyMap, and CGAP SAGE, Sets of similar genes according to GeneDecks, in vivo and in vitro expression data from LifeMap Discovery™, plus additional links to Genevestigator, and/or SOURCE, and/or BioGPS, and/or UniProtKB,
    PCR Arrays from SABiosciences, Primers from OriGene, SABiosciences, and/or QIAGEN, In Situ Hybridization Assays from Advanced Cell Diagnostics)
    About This Section

    SLC26A7 expression in normal human tissues (normalized intensities)
    See probesets specificity/sensitivity at GeneAnnot
    About this imageBioGPS
    CGAP TAG: GAAATAAATC

    Microarray
    RNAseq (Illumina Body Map)
    (100×FPKM)½
    SAGE (Serial Analysis of Gene Expression)
    About this image

    SLC26A7 expression in embryonic tissues and stem cells
    Expression by the Database of Embryonic development, Stem cell research, and Regenerative medicine    About this table
    9 LifeMap In Vivo Development Anatomical Compartments/Cells 
    Tissue Anatomical Compartment CellCategory (developmental path)
    LimbZeugopodMesenchymal Condensate CellsBone, Cartilage
    OvaryPrimary FollicleGranulosa CellsOvary
    OvaryPrimordial FolliclePre-Granulosa CellsOvary
    BoneZeugopod Long BoneBone
    KidneyMetanephrosKidney
    LimbAutopodLimb
    LimbZeugopodLimb
    Reproductive SystemVas DeferensReproductive System
    Skeletal MuscleExtraocular MusclesSkeletal Muscle
    Expression: Positive    Negative     Selective marker
    Experimental details: Curated     Microarrays     In-situ hybridization

    See SLC26A7 Protein Expression from SPIRE MOPED and PaxDB
    Genevestigator expression for SLC26A7

    SOURCE GeneReport for Unigene cluster: Hs.354013

    UniProtKB/Swiss-Prot: S26A7_HUMAN, Q8TE54
    Tissue specificity: Expressed in tonsillar high endothelial venule endothelial cells (HEVEC), placenta and in testis,
    expressed in a subgroup of basal cells in the epididymal ducts

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    In Situ
    Assay Products:     
         		Advanced Cell Diagnostics RNAscope RNA in situ hybridization assays for SLC26A7

    Orthologs
    for SLC26A7 gene

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

    Orthologs for SLC26A7 gene from 5/19 species (see all 19)    About this table
    Organism Taxonomic
    classification    		 Gene Description Human
    Similarity    		 Orthology
    Type    		 Details
    chicken
    (Gallus gallus)    		 Aves SLC26A71 solute carrier family 26, member 7 73.89(n)
    75.35(a)    		   428369  XM_425930.3  XP_425930.3 
    lizard
    (Anolis carolinensis)    		 Reptilia SLC26A76
    		 --
    		 74(a)
    		 1 ↔ 1
    		 4(17454167-17538801)
    fruit fly
    (Drosophila melanogaster)    		 Insecta Prestin6
    		 Prestin
    		 21(a)
    		 possible ortholog
    		 3L(17891989-17900912)
    worm
    (Caenorhabditis elegans)    		 Secernentea W04G3.63 dra like protein 34(a)
    (best of 6)    		   X(11115908-11117663)   --
    thale cress
    (Arabidopsis thaliana)    		 eudicotyledons SULTR3;21 sulfate transporter 3.2 40.82(n)
    27.12(a)    		   828201  NM_116504.3  NP_192179.1 


    ENSEMBL Gene Tree for SLC26A7 (if available)
    TreeFam Gene Tree for SLC26A7 (if available) 

    Paralogs
    for SLC26A7 gene

    (Paralogs according to 1HomoloGene,
    2Ensembl, and 3SIMAP, Pseudogenes according to 4Pseudogene.org Build 68)
    About This Section
    Paralogs for SLC26A7 gene
    SLC26A92  SLC26A32  SLC26A62  SLC26A12  SLC26A52  SLC26A22  SLC26A112  SLC26A102  
    SLC26A42  SLC26A82  
    10 SIMAP similar genes for SLC26A7 using alignment to 4 protein entries:     S26A7_HUMAN (see all proteins):
    SLC26A6    SLC26A4    SLC26A5    SLC26A10    SLC26A3    SLC26A9
    DKFZp686P10213    SLC26A2    PRES    RESDA1

    SLC26A7 for paralogs           About GeneDecksing



    Genomic Variants
    for SLC26A7 gene

    (SNPs/Variants according to the 1NCBI SNP Database, 2Ensembl, 3PupaSUITE, UniProtKB, and DNA2.0, Linkage Disequilibrium by HapMap, Structural Variations(CNVs/InDels/Inversions) from the Database of Genomic Variants, Mutations from the Human Gene Mutation Database (HGMD) and the Locus Specific Mutation Databases (LSDB), Blood group antigen gene mutations by BGMUT, Resequencing Primers from QIAGEN, Cancer Mutation PCR Arrays and Assays and Copy Number PCR Arrays from SABiosciences)
    About This Section

    10/2247 NCBI SNPs in SLC26A7 are shown (see all 2247)     About this table
    Genomic DataTranscription Related DataAllele Frequencies
    SNP IDValidClinical
    significance    		Chr 8 posSequence#AA
    Chg    		TypeMore#Allele
    freq    		PopTotal
    sample    		More
    ----------
    rs339337611,2
    		C,--92259752(+) AAAAA-/CATCTG 2 -- us2k10--------
    rs636481631,2
    		--92259752(+) AAAAAC/AATCTG 2 -- us2k11Minor allele frequency- A:0.50NA 2
    rs1889480721,2
    		--92259793(+) AAGATG/TTTTAG 2 -- us2k10--------
    rs1923529751,2
    		--92259822(+) TTAAGA/GAATTT 2 -- us2k10--------
    rs736971611,2
    		C,--92259958(+) TGTTCA/TTGTGA 2 -- us2k12Minor allele frequency- T:0.06WA 120
    rs1842564941,2
    		--92259963(+) ATGTGA/CATTTT 2 -- us2k10--------
    rs1888591241,2
    		--92260016(+) CACAAA/GTGATA 2 -- us2k10--------
    rs117872251,2
    		C,F,A,H,--92260023(+) GATAGA/TTGTTG 2 -- us2k116Minor allele frequency- T:0.38NS EA NA WA 1266
    rs101125201,2
    		C,F,H,--92260029(+) TGTTGA/GTTGGT 2 -- us2k16Minor allele frequency- G:0.06NS EA WA NA 656
    rs736971621,2
    		C,--92260085(+) CGTTAG/TAATTT 2 -- us2k12Minor allele frequency- T:0.06WA 120

    HapMap Linkage Disequilibrium report for SLC26A7 (92221722 - 92410378 bp)
    Structural Variations (Copy Number Variations, Insertions/Deletions, Inversions)
    Database of Genomic Variants (DGV): 1 variation for SLC26A7
         1 CNV: 3741

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    Disorders / Diseases
    for SLC26A7 gene

    (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
    SLC26A7 for disorders           About GeneDecksing

    OMIM gene information: 608479    OMIM disorders: --

    14 diseases for SLC26A7:    About MalaCards
    ventricular septal defect    congenital dyserythropoietic anemia    diastrophic dysplasia    dyserythropoietic anemia
    fainting    epididymitis    pharyngitis    anemia
    hypertension    schizophrenia    tuberculosis    malaria
    neuronitis    mycobacterium tuberculosis

    1 disease from the University of Copenhagen DISEASES database for SLC26A7:
    Diastrophic dysplasia

    Export disorders for SLC26A7 gene to outside databases

    Publications
    for SLC26A7 gene

    (in PubMed. Associations of this gene to articles via 1Entrez Gene, 2UniProtKB/Swiss-Prot, 3HGNC, 4GAD, 5PharmGKB, 6HMDB, 7DrugBank, 8UniProtKB/TrEMBL, 9 Novoseek, and/or 10fRNAdb)
    About This Section

    PubMed articles for SLC26A7 gene, integrated from 9 sources (see all 14):
    (articles sorted by number of sources associating them with SLC26A7)    		    Utopia: connect your pdf to the dynamic
    world of online information

    1. Molecular cloning of SLC26A7, a novel member of the SLC26 sulfate/anion transporter family, from high endothelial venules and kidney. (PubMed id 11829495)1, 2, 3, 9 Vincourt J.-B.... Girard J.-P. (2002)
    2. Chloride/bicarbonate exchanger SLC26A7 is localized in endosomes in medullary collecting duct cells and is targeted to the basolateral membrane in hypertonicity and potassium depletion. (PubMed id 16524946)1, 2, 3 Xu J....Soleimani M. (2006)
    3. Functional characterization of three novel tissue-specific anion exchangers SLC26A7, -A8, and -A9. (PubMed id 11834742)1, 2, 3 Lohi H.... Kere J. (2002)
    4. SLC26A6 and SLC26A7 anion exchangers have a distinct distribution in human kidney. (PubMed id 15956810)1, 2 Kujala M....Kere J. (2005)
    5. Identification of a basolateral Cl-/HCO3- exchanger specific to gastric parietal cells. (PubMed id 12736153)1, 2 Petrovic S.... Soleimani M. (2003)
    6. Exome sequencing supports a de novo mutational paradi gm for schizophrenia. (PubMed id 21822266)1 Xu B....Karayiorgou M. (2011)
    7. Expression of ion transport-associated proteins in human efferent and epididymal ducts. (PubMed id 17504921)2 Kujala M.... Hoglund P. (2007)
    8. The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC). (PubMed id 15489334)2 Gerhard D.S....Malek J. (2004)
    9. Differential regulation of basolateral Cl-/HCO3- exchangers SLC26A7 and AE1 in kidney outer medullary collecting duct. (PubMed id 15284286)1 Barone S....Soleimani M. (2004)
    10. Complete sequencing and characterization of 21,243 full-length human cDNAs. (PubMed id 14702039)1 Ota T.... Sugano S. (2004)

    External Searches for SLC26A7 gene

    (in PubMed, OMIM, and NCBI Bookshelf)
    About This Section
     ANDOR
    Aliases
    Free Text  
      Query String
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    NCBI Bookshelf
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    Genome Databases showing SLC26A7 gene

    (According to Entrez Gene, HGNC, AceView, euGenes, Ensembl, miRBase, ECgene, Kegg, and/or H-InvDB)
    About This Section
    Entrez Gene: 115111 HGNC: 14467 AceView: CGI-77andSLC26A7 Ensembl:ENSG00000147606 euGenes: HUgn115111
    ECgene: SLC26A7 Kegg: 115111 H-InvDB: SLC26A7

    Other Databases showing SLC26A7 gene

    (According to HUGE)
    About This Section
    		   --

    Specialized Databases showing SLC26A7 gene

    (According to PharmGKB, ATLAS, HORDE, IMGT, LEIDEN, UniProtKB/Swiss-Prot, and/or UniProtKB/TrEMBL,
    Wikipedia and/or GeneReviews via UniProtKB/Swiss-Prot)
    About This Section
    NameDescription
    PharmGKB entry for SLC26A7 Pharmacogenomics, SNPs, Pathways

    Intellectual Property
    for SLC26A7 gene

    (Patent information from GeneIP,
    Licensable technologies from WIS Yeda, Salk, Tufts,
    IP news from LifeMap Sciences, Inc.)
    About This Section
    		Patent Information for SLC26A7 gene:
    Search GeneIP for patents involving SLC26A7

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



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