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

SLC22A13 Gene

protein-coding   GIFtS: 44
GCID: GC03P038307

solute carrier family 22 (organic anion transporter), member...

(Previous name: organic cationic transporter-like 3 )
(Previous symbol: ORCTL3)
  Search for SLC22A13
in our new
 Human Malady Compendium 
Biological research products
for SLC22A13
    

(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 22 (Organic Anion Transporter), Member 131 2     Organic Cation Transporter-Like 32 3
ORCTL31 2 3     ORCTL-32 3
OAT101 2     Organic-Cation Transporter Like 32
OCTL11 2     Solute Carrier Family 22 Member 132
OCTL31 2     Solute Carrier Family 22, Member 132
Organic Cationic Transporter-Like 31 2     

External Ids:    HGNC: 84941   Entrez Gene: 93902   Ensembl: ENSG000001729407   OMIM: 6040475   UniProtKB: Q9Y2263   

Export aliases for SLC22A13 gene to outside databases

Previous GC identifers: GC00U912985 GC03P038267 GC03P038282


(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 SLC22A13:
This gene encodes a member of the organic-cation transporter family. It is located in a gene cluster with another
member of the family, organic cation transporter like 4. The encoded protein is a transmembrane protein involved in
the transport of small molecules. This protein can function to mediate urate uptake and is a high affinity nicotinate
exchanger in the kidneys and the intestine. (provided by RefSeq, Sep 2008)




(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_000003.11  NC_018914.1  NT_022517.18  
Regulatory elements:
   SABiosciences Regulatory transcription factor binding sites in the SLC22A13 gene promoter:
         USF1   AML1a   USF-1   HNF-1   IRF-7A   HNF-1A   Evi-1   GATA-1   
         Other transcription factors

SwitchGear Promoter luciferase reporter plasmidSLC22A13 promoter sequence
   Search SABiosciences Chromatin IP Primers for SLC22A13

Epigenetics:
QIAGEN PyroMark CpG Assay predesigned Pyrosequencing DNA Methylation assays in human, mouse, rat SLC22A13


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

Entrez Gene cytogenetic band: 3p21.3   Ensembl cytogenetic band:  3p22.2   HGNC cytogenetic band: 3p22.2

SLC22A13 Gene in genomic location: bands according to Ensembl, locations according to (and/or Entrez Gene and/or Ensembl if different)
SLC22A13 gene location

GeneLoc information about chromosome 3         GeneLoc Exon Structure

GeneLoc location for GC03P038307:  view genomic region     (about GC identifiers)

Start:
38,307,298 bp from pter      End:
38,319,806 bp from pter
Size:
12,509 bases      Orientation:
plus strand

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

UniProtKB/Swiss-Prot: S22AD_HUMAN, Q9Y226 (See protein sequence)
Recommended Name: Solute carrier family 22 member 13  
Size: 551 amino acids; 60862 Da
Subcellular location: Membrane; Multi-pass membrane protein (Potential)
Secondary accessions: B2RCV9 Q8IYG1
Alternative splicing: 2 isoforms:  Q9Y226-1   Q9Y226-2   

Explore the universe of human proteins at neXtProt for SLC22A13: NX_Q9Y226

Post-translational modifications:

  • View modification sites using PhosphoSitePlus2
  • View neXtProt modification sites for NX_Q9Y226

  • SLC22A13 Protein expression data from MOPED and PaxDb:    About this image 
    SLC22A13 Protein Expression
    REFSEQ proteins: NP_004247.2  
    ENSEMBL proteins: 
     ENSP00000310241   ENSP00000395106   ENSP00000406929  

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    Uscn Proteins for SLC22A13

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

    GO IDQualified GO termEvidencePubMed IDs
    GO:0005887integral to plasma membrane NAS10072596

    SLC22A13 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

    SLC22A13 for domains           About GeneDecksing

    3 InterPro domains/families:
     IPR005828 Sub_transporter
     IPR020846 MFS_dom
     IPR016196 MFS_dom_general_subst_transpt

    Graphical View of Domain Structure for InterPro Entry Q9Y226

    ProtoNet protein and cluster: Q9Y226

    UniProtKB/Swiss-Prot: S22AD_HUMAN, Q9Y226
    Similarity: Belongs to the major facilitator (TC 2.A.1) superfamily. Organic cation transporter (TC 2.A.1.19) family


    (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

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

    GO IDQualified GO termEvidencePubMed IDs
    GO:0015101organic cation transmembrane transporter activity NAS10072596
         
    SLC22A13 for ontologies           About GeneDecksing


    Animal Models:
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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



    Interactions:

        Search SABiosciences Gene Network CentralTM Interacting Genes and Proteins Networks for SLC22A13

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

    GO IDQualified GO termEvidencePubMed IDs
    GO:0015695organic cation transport NAS10072596

    SLC22A13 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 SLC22A13
    Search CenterWatch for drugs/clinical trials and news about SLC22A13 / S22AD 

    (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,
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    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 SLC22A13 gene: 
    NM_004256.3  

    Unigene Cluster for SLC22A13:

    Solute carrier family 22 (organic anion transporter), member 13
    Hs.225941  [show with all ESTs]
    Unigene Representative Sequence: NM_004256
    3 Ensembl transcripts including schematic representations, and UCSC links where relevant:
    ENST00000311856(uc011aym.1 uc011ayn.1 uc003chz.3) ENST00000415844
    ENST00000450935

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    hsa-miR-1252 hsa-miR-26b*
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    Inhib. RNA
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    Additional cDNA sequence: 

    AB010438.1 AK315301.1 

    2 DOTS entries:

    DT.100000451  DT.75193280 

    11 AceView cDNA sequences:

    BI517655 BC035973 AB010438 NM_004256 AI934403 BE326882 BF589890 BF510842 
    BF476068 BG432776 BI518368 

    GeneLoc Exon Structure

    2 Alternative Splicing Database (ASD) splice patterns (SP) for SLC22A13    About this scheme

    ExUns: 1a · 1b ^ 2 ^ 3 ^ 4a · 4b ^ 5 ^ 6 ^ 7 ^ 8 ^ 9 ^ 10
    SP1:                                                                        
    SP2:                    -                                                   


    ECgene alternative splicing isoforms for SLC22A13

    (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

    SLC22A13 expression in normal human tissues (normalized intensities)
    See probesets specificity/sensitivity at GeneAnnot
    About this imageBioGPS
    CGAP TAG: CAGGGTGAGG
    SLC22A13 Expression
    About this image
    See SLC22A13 Protein Expression from SPIRE MOPED and PaxDB
    Genevestigator expression for SLC22A13

    SOURCE GeneReport for Unigene cluster: Hs.225941

    UniProtKB/Swiss-Prot: S22AD_HUMAN, Q9Y226
    Tissue specificity: Ubiquitous, expressed at low levels

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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 SLC22A13 gene from 5/17 species (see all 17)    About this table
    Organism Taxonomic
    classification
    Gene Description Human
    Similarity
    Orthology
    Type
    Details
    chicken
    (Gallus gallus)
    Aves SLC22A131 solute carrier family 22 (organic anion transporter), more 58.57(n)
    50.28(a)
      420423  XM_418529.3  XP_418529.2 
    lizard
    (Anolis carolinensis)
    Reptilia --
    --
    --
    47(a)
    46(a)
    many ↔ many
    many ↔ many
    6(738322-752743)
    6(766807-782091)
    zebrafish
    (Danio rerio)
    Actinopterygii zgc:1536391 zgc:153639 53.68(n)
    47.5(a)
      556601  NM_001077372.2  NP_001070840.2 
    fruit fly
    (Drosophila melanogaster)
    Insecta CG60066
    CG89256
    (see all 6)
    --
    22(a)
    18(a)
    (see all 6)
    many ↔ many
    many ↔ many
    (see all 6)
    3R(11981040-11997488)
    3R(11997731-12006200)
    worm
    (Caenorhabditis elegans)
    Secernentea T12B3.26
    B0252.36
    (see all 24)
    Putative transporter B0252.3
    (see all 24)
    21(a)
    20(a)
    (see all 24)
    possible ortholog
    possible ortholog
    (see all 24)
    IV(7376886-7378889)
    II(6902826-6907713)


    ENSEMBL Gene Tree for SLC22A13 (if available)
    TreeFam Gene Tree for SLC22A13 (if available) 

    (Paralogs according to 1HomoloGene,
    2Ensembl, and 3SIMAP, Pseudogenes according to 4Pseudogene.org Build 68)
    About This Section
    Paralogs for SLC22A13 gene
    SLC22A112  SLC22A52  SLC22A82  SLC22A12  SLC22A242  SLC22A42  SLC22A92  SLC22A22  
    SLC22A102  SLC22A62  SLC22A152  SLC22A72  SLC22A122  SLC22A32  SLC22A252  SLC22A162  
    18/20 SIMAP similar genes for SLC22A13 using alignment to 3 protein entries:     S22AD_HUMAN (see all proteins) (see all similar genes):
    SLC22A15    SLC22A8    SLC22A14    SLC22A6    HMFN2567    SLC22A12
    SLC22A25    SLC22A7    SLC22A11    OAT7    SLC22A10    SLC22A20
    SLC22A9    SLC22A2    SLC22A1    SLC22A24    SLC22A3    SLC22A4

    SLC22A13 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

    10/282 NCBI SNPs in SLC22A13 are shown (see all 282    About this table
    Genomic DataTranscription Related DataAllele Frequencies
    SNP IDValidClinical
    significance
    Chr 3 posSequence#AA
    Chg
    TypeMore#Allele
    freq
    PopTotal
    sample
    More
    ----------
    rs787253441,2
    F--38305450(+) AATTGT/GACACC 1 -- us2k11Minor allele frequency- G:0.04NA 120
    rs1489669841,2
    --38305481(+) GAGACC/GATCCT 1 -- us2k10--------
    rs1442824461,2
    --38305495(+) CCTAGA/GTGGGG 1 -- us2k10--------
    rs1154638531,2
    F--38305509(+) TTGAGG/AGCCAG 1 -- us2k11Minor allele frequency- A:0.04WA 118
    rs730628781,2
    C,F--38305979(+) TGGCCA/CGGGCT 1 -- us2k11Minor allele frequency- C:0.02NA 120
    rs1465574731,2
    --38306143(+) GGTGGA/GGGCAT 1 -- us2k10--------
    rs98500461,2
    C--38306147(+) GAGGCC/ATACTT 1 -- us2k11Minor allele frequency- A:0.50WA 2
    rs2029901,2
    C,H--38306200(+) GGTACT/GTGCAT 1 -- us2k116Minor allele frequency- G:0.00EA NA WA CSA 128
    rs1888486351,2
    --38306299(+) GTTTGC/TCTTTG 1 -- us2k10--------
    rs760593961,2
    C,F--38306623(+) TGTCTC/GATTTG 1 -- us2k12Minor allele frequency- G:0.03WA NA 238

    HapMap Linkage Disequilibrium report for SLC22A13 (38307298 - 38319806 bp)
    Structural Variations (Copy Number Variations, Insertions/Deletions, Inversions)
          Database of Genomic Variants (DGV) variations for SLC22A13: --

    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, Genatlas, GeneTests, GAD, HuGE Navigator, and/or TGDB.)
    About This Section

    SLC22A13 for disorders           About MalaCards

    SLC22A13 for disorders           About GeneDecksing

    OMIM gene information: 604047    OMIM disorders: --

    Human Genome Epidemiology (HuGE) Navigator: SLC22A13 (2 documents)

    Export disorders for SLC22A13 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 SLC22A13 gene, integrated from 9 sources (see all 11):
    (articles sorted by number of sources associating them with SLC22A13)
        Utopia: connect your pdf to the dynamic
    world of online information

    1. Molecular cloning, mapping, and characterization of two novel human genes, ORCTL3 and ORCTL4, bearing homology to organic-cation transporters. (PubMed id 10072596)1, 2, 3, 9 Nishiwaki T.... Nakamura Y. (1998)
    2. Identification of a new urate and high affinity nicotinate transporter, hOAT10 (SLC22A13). (PubMed id 18411268)1, 3, 9 Bahn A....Burckhardt G. (2008)
    3. Characterization of a 1200-kb genomic segment of chromosome 3p22- p21.3. (PubMed id 10231028)1, 2, 9 Daigo Y.... Nakamura Y. (1999)
    4. The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC). (PubMed id 15489334)1, 2 Gerhard D.S....Malek J. (2004)
    5. Isolation of ORCTL3 in a novel genetic screen for tumor-specific apoptosis inducers. (PubMed id 19282870)1, 9 Irshad S....Grimm S. (2009)
    6. Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score. (PubMed id 20379614)1 Rose J.E....Uhl G.R. (2010)
    7. The effects of genetic polymorphisms in the organic c ation transporters OCT1, OCT2, and OCT3 on the renal clearance of metformin. (PubMed id 19536068)1 Tzvetkov M.V....BrockmAPller J. (2009)
    8. Diversification of transcriptional modulation: large-scale identification and characterization of putative alternative promoters of human genes. (PubMed id 16344560)1 Kimura K.... Sugano S. (2006)
    9. Complete sequencing and characterization of 21,243 full-length human cDNAs. (PubMed id 14702039)2 Ota T.... Sugano S. (2004)
    10. Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences. (PubMed id 12477932)1 Strausberg R.L....Marra M.A. (2002)

    (in PubMed, OMIM, and NCBI Bookshelf)
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    (According to Entrez Gene, HGNC, AceView, euGenes, Ensembl, miRBase, ECgene, Kegg, and/or H-InvDB)
    About This Section
    Entrez Gene: 9390 HGNC: 8494 AceView: SLC22A13 Ensembl:ENSG00000172940 euGenes: HUgn9390
    ECgene: SLC22A13 H-InvDB: SLC22A13

    (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 SLC22A13 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 SLC22A13 gene:
    Search GeneIP for patents involving SLC22A13

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



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