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SLC22A23 Gene

protein-coding   GIFtS: 46
GCID: GC06M003269

Solute Carrier Family 22, Member 23

(Previous name: chromosome 6 open reading frame 85)
(Previous symbol: C6orf85)
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(According to 1HGNC, 2Entrez Gene,
3UniProtKB/Swiss-Prot, 4UniProtKB/TrEMBL, 5OMIM, 6GeneLoc, 7Ensembl, 8DME, 9miRBase, 10fRNAdb, 12H-InvDB, 13NCBI, 14NONCODE, and/or 15RNAdb)
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Aliases
Solute Carrier Family 22, Member 231 2
C6orf851 2 3 5
Chromosome 6 Open Reading Frame 851
Ion Transporter Protein2
Solute Carrier Family 22 Member 232

External Ids:    HGNC: 211061   Entrez Gene: 630272   Ensembl: ENSG000001372667   OMIM: 6116975   UniProtKB: A1A5C73   

Export aliases for SLC22A23 gene to outside databases

Previous GC identifers: GC06M003216 GC06M003147


(According to Entrez Gene, GeneCards, Tocris Bioscience, Wikipedia's Gene Wiki, PharmGKB,
UniProtKB/Swiss-Prot, and/or UniProtKB/TrEMBL)
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Entrez Gene summary for SLC22A23 Gene:
SLC22A23 belongs to a large family of transmembrane proteins that function as uniporters, symporters, and
antiporters to transport organic ions across cell membranes (Jacobsson et al., 2007 (PubMed 17714910)).(supplied
by OMIM, Mar 2008)

GeneCards Summary for SLC22A23 Gene:
SLC22A23 (solute carrier family 22, member 23) is a protein-coding gene. GO annotations related to this gene include transmembrane transporter activity. An important paralog of this gene is SLC22A17.




(According to GeneLoc and/or HGNC, and/or
Entrez Gene (NCBI build 37),
and/or miRBase,
Genomic Views according to UCSC (hg19) and Ensembl (release 75), Regulatory elements and Epigenetics data according to QIAGEN, and/or SwitchGear Genomics)
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Regulatory elements:
   Regulatory transcription factor binding sites in the SLC22A23 gene promoter:
         Sox5   SREBP-1c   Egr-4   Arnt   SREBP-1b   PPAR-gamma1   SREBP-1a   PPAR-gamma2   
         Other transcription factors

SwitchGear Promoter luciferase reporter plasmidSLC22A23 promoter sequence
   Search Chromatin IP Primers for SLC22A23

Epigenetics:
DNA Methylation CpG Assay Predesigned for Pyrosequencing in human, mouse, rat SLC22A23


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

Entrez Gene cytogenetic band: 6p25.2   Ensembl cytogenetic band:  6p25.2   HGNC cytogenetic band: 6p25.2

SLC22A23 Gene in genomic location: bands according to Ensembl, locations according to (and/or Entrez Gene and/or Ensembl if different)
SLC22A23 gene location

GeneLoc information about chromosome 6         GeneLoc Exon Structure

GeneLoc location for GC06M003269:  view genomic region     (about GC identifiers)

Start:
3,269,196 bp from pter      End:
3,457,256 bp from pter
Size:
188,061 bases      Orientation:
minus strand

(According to 1UniProtKB, HORDE, 2neXtProt, Ensembl, and/or Reactome, Modification sites according to PhosphoSitePlus, Specific Peptides from DME, RefSeq according to NCBI, PDB rendering according to OCA and/or Proteopedia, Recombinant Proteins from EMD Millipore, R&D Systems, GenScript, Enzo Life Sciences, OriGene, Novus Biologicals, Sino Biological, ProSpec, Cloud-Clone Corp., eBioscience, and/or antibodies-online,
Biochemical Assays by EMD Millipore, R&D Systems, OriGene, GenScript, Cell Signaling Technology, Enzo Life Sciences, Cloud-Clone Corp., eBioscience, and/or antibodies-online, Antibodies by EMD Millipore, R&D Systems, Cell Signaling Technology, OriGene, Novus Biologicals, Thermo Fisher Scientific, Abcam, Cloud-Clone Corp, antibodies-online, and/or others.)
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UniProtKB/Swiss-Prot: S22AN_HUMAN, A1A5C7 (See protein sequence)
Recommended Name: Solute carrier family 22 member 23  
Size: 686 amino acids; 73748 Da
Sequence caution: Sequence=BAD18753.1; Type=Erroneous initiation; Sequence=CAI12303.1; Type=Erroneous gene model
prediction; Sequence=CAI40959.1; Type=Erroneous gene model prediction;
Secondary accessions: A1A5C8 Q5T8B8 Q6ZMH3 Q8IW73
Alternative splicing: 4 isoforms:  A1A5C7-1   A1A5C7-2   A1A5C7-3   A1A5C7-4   (No experimental confirmation available)

Explore the universe of human proteins at neXtProt for SLC22A23: NX_A1A5C7

Explore proteomics data for SLC22A23 at MOPED

Post-translational modifications: 

  • Glycosylation2 at Asn24, Thr143, Asn279
  • Modification sites at PhosphoSitePlus

  • See SLC22A23 Protein Expression from SPIRE MOPED, PaxDB, and MaxQB

    REFSEQ proteins (4 alternative transcripts): 
    NP_001273384.1  NP_001273385.1  NP_056297.1  NP_068764.3  

    ENSEMBL proteins: 
     ENSP00000410245   ENSP00000385028   ENSP00000417737   ENSP00000369657   ENSP00000419463  
     ENSP00000418134   ENSP00000418985   ENSP00000369653  

    SLC22A23 Human Recombinant Protein Products:

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    Cloud-Clone Corp. Proteins for SLC22A23

     
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    antibodies-online peptides for SLC22A23

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    antibodies-online antibodies for SLC22A23 (3 products) 

    SLC22A23 Assay Products:

    Browse Kits and Assays available from EMD Millipore
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    Cloud-Clone Corp. ELISAs for SLC22A23
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    Search eBioscience for ELISAs for SLC22A23 
    antibodies-online kits for SLC22A23 (6 products) 


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

    IUPHAR Guide to PHARMACOLOGY protein family classification: SLC22A23
    Orphan or poorly characterized SLC22 family members

    4 InterPro protein domains:
     IPR005829 Sugar_transporter_CS
     IPR005828 Sub_transporter
     IPR020846 MFS_dom
     IPR016196 MFS_dom_general_subst_transpt

    Graphical View of Domain Structure for InterPro Entry A1A5C7

    ProtoNet protein and cluster: A1A5C7

    UniProtKB/Swiss-Prot: S22AN_HUMAN, A1A5C7
    Similarity: Belongs to the major facilitator (TC 2.A.1) superfamily. Organic cation transporter (TC 2.A.1.19)
    family


    Find genes that share domains with SLC22A23           About GenesLikeMe


    (According to 1UniProtKB, Genatlas, LifeMap Discovery™, IUBMB, and/or 2DME, Human phenotypes from GenomeRNAi, Animal models from MGI Mar 06 2013, genOway,
    transcription factor targeting from QIAGEN and/or HOMER, miRNA Gene Targets from miRTarBase, shRNA from OriGene, siRNAs from OriGene, QIAGEN, microRNA from QIAGEN, SwitchGear Genomics, Gene Editing from DNA2.0, Clones from OriGene, GenScript, Sino Biological, DNA2.0, Vector BioLabs and/or Addgene, Cell Lines from GenScript, ESI BIO, In Situ Hybridization Assays from Advanced Cell Diagnostics, Flow cytometry from eBioscience, Ontologies according to Gene Ontology Consortium 01 Apr 2014 via Entrez Gene.)
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         Gene Ontology (GO): 1 molecular function term:    About this table

    GO IDQualified GO termEvidencePubMed IDs
    GO:0022857transmembrane transporter activity IEA--
         
    Find genes that share ontologies with SLC22A23           About GenesLikeMe


    Phenotypes:
         1 GenomeRNAi human phenotype for SLC22A23:
     Increased viability after born 

    Animal Models:
       genOway: Develop your customized and physiologically relevant rodent model for SLC22A23

    miRNA
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    miRTarBase miRNAs that target SLC22A23:
    hsa-mir-3127-5p (MIRT052658), hsa-mir-378a-3p (MIRT043940)

    Block miRNA regulation of human, mouse, rat SLC22A23 using miScript Target Protectors
    Selected qRT-PCR Assays for microRNAs that regulate SLC22A23 (see all 109):
    hsa-miR-323-3p hsa-miR-100* hsa-miR-520e hsa-miR-520f hsa-miR-3607-3p hsa-miR-106a hsa-miR-128 hsa-miR-938
    Browse SwitchGear 3'UTR luciferase reporter plasmids
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    GenScript: all cDNA clones in your preferred vector (see all 2): SLC22A23 (NM_021945)
    Browse Sino Biological Human cDNA Clones
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    Advanced Cell Diagnostics RNAscope RNA in situ hybridization assays for SLC22A23


    (According to UniProtKB, COMPARTMENTS Subcellular localization database, Ontologies according to Gene Ontology Consortium 01 Apr 2014 via Entrez Gene.)
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    Subcellular locations from UniProtKB/Swiss-Prot
    S22AN_HUMAN, A1A5C7: Membrane; Multi-pass membrane protein (Potential)
    Subcellular locations from COMPARTMENTS: 

    CompartmentConfidence
    plasma membrane3
    cytosol1
    golgi apparatus1
    nucleus1

    Gene Ontology (GO): 1 cellular component term:    About this table

    GO IDQualified GO termEvidencePubMed IDs
    GO:0016021integral component of membrane IEA--

    Find genes that share ontologies with SLC22A23           About GenesLikeMe


    (SuperPaths according to PathCards, Pathways according to R&D Systems, Cell Signaling Technology, KEGG, PharmGKB, BioSystems, Sino Biological, Reactome, Tocris Bioscience, GeneGo (Thomson Reuters), QIAGEN, and/or UniProtKB, Sets of similar genes according to GeneDecks, Interaction Networks according to QIAGEN, and/or STRING, Interactions according to 1UniProtKB, 2MINT, 3I2D, and/or 4STRING, with links to IntAct and Ensembl, Ontologies according to Gene Ontology Consortium 01 Apr 2014 via Entrez Gene).
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        Custom Pathway & Disease-focused RT2 Profiler PCR Arrays for SLC22A23
    Interactions:

        Search GeneGlobe Interaction Network for SLC22A23

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

    1 Interacting protein for SLC22A23 (ENSP000003850284) via UniProtKB, MINT, STRING, and/or I2D
    InteractantInteraction Details
    GeneCardExternal ID(s)
    UBCENSP000003448184STRING: ENSP00000344818
    About this table

    Gene Ontology (GO): 2 biological process terms:    About this table

    GO IDQualified GO termEvidencePubMed IDs
    GO:0006811ion transport IEA--
    GO:0055085transmembrane transport ----

    Find genes that share ontologies with SLC22A23           About GenesLikeMe



    (Chemical Compounds according to UniProtKB, Enzo Life Sciences, EMD Millipore, Tocris Bioscience, ApexBio, HMDB, BitterDB, and/or Novoseek, Ligands according to IUPHAR, and Drugs according to DrugBank, Enzo Life Sciences, and/or PharmGKB)
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    Browse Small Molecules at EMD Millipore
       Browse drugs & compounds from Enzo Life Sciences
      Browse compounds at ApexBio 

    Browse Tocris compounds for SLC22A23 (S22AN)



    (Secondary structures according to fRNAdb,
    GenBank/EMBL/DDBJ Accessions according to
    Unigene (Build 236 Homo sapiens; Apr 25 2013) or GenBank,
    RefSeq according to Entrez Gene,
    DOTS (version 10), and/or AceView, transcript ids from Ensembl with links to UCSC,
    exon structure from GeneLoc, alternative splicing isoforms according to ASD and/or ECgene,
    siRNAs from OriGene, QIAGEN, shRNA from OriGene, microRNA from QIAGEN, SwitchGear Genomics,
    Tagged/untagged cDNA clones from OriGene, GenScript, DNA2.0, Vector BioLabs, and/or Addgene, Primers from OriGene, and/or QIAGEN, Flow cytometry from eBioscience )
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    REFSEQ mRNAs for SLC22A23 gene (4 alternative transcripts): 
    NM_001286455.1  NM_001286456.1  NM_015482.1  NM_021945.6  

    12 Ensembl transcripts including schematic representations, and UCSC links where relevant:
    ENST00000436008(uc003mvn.3 uc003mvo.3 uc003mvm.3) ENST00000406686(uc010jnn.3)
    ENST00000497691(uc003mvp.1) ENST00000380302 ENST00000490273 ENST00000482874
    ENST00000485307 ENST00000467177 ENST00000467144 ENST00000496753 ENST00000433689
    ENST00000380298(uc010jno.2)
    miRNA
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    Selected qRT-PCR Assays for microRNAs that regulate SLC22A23 (see all 109):
    hsa-miR-323-3p hsa-miR-100* hsa-miR-520e hsa-miR-520f hsa-miR-3607-3p hsa-miR-106a hsa-miR-128 hsa-miR-938
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      QuantiTect SYBR Green Assays in human, mouse, rat SLC22A23
      QuantiFast Probe-based Assays in human, mouse, rat SLC22A23

    Selected AceView cDNA sequences (see all 198):

    AI867904 Z41786 CD722175 BM993128 AI446649 BM980165 AI888634 BU739429 
    CR610126 W80733 AI632136 CB161497 AW291160 NM_021945 AI362326 AW136148 
    Z45225 AL110245 AK172770 AA339438 AI989962 F05032 BC040876 BF062357 

    GeneLoc Exon Structure


    (RNA expression data according to H-InvDB, NONCODE, miRBase, and RNAdb, Expression images according to data from BioGPS, Illumina Human BodyMap, and CGAP SAGE, Sets of similar genes according to GeneDecks, in vivo and in vitro expression data from LifeMap Discovery™, Protein expression images according to data from SPIRE 1MOPED, 2PaxDb, and 3MaxQB, plus additional links to SOURCE, and/or BioGPS, and/or UniProtKB,
    PCR Arrays from QIAGEN, Primers from OriGene, and/or QIAGEN, In Situ Hybridization Assays from Advanced Cell Diagnostics)
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    SLC22A23 expression in normal human tissues (normalized intensities)
    See probesets specificity/sensitivity at GeneAnnot
    About this imageBioGPS <intensity>2/3
    CGAP TAG: GTGTCGCATC
    SLC22A23 Expression
    About this image


    SLC22A23 expression in embryonic tissues and stem cells    About this table
    Data from LifeMap, the Embryonic Development and Stem Cells Database
     
     Blood (Hematopoietic System)
             Proerythroblasts Hematopoietic Bone Marrow
    SLC22A23 Protein expression data from MOPED1, PaxDb2 and MaxQB3    About this image

    SLC22A23 Protein Expression
        Custom PCR Arrays for SLC22A23
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    In Situ
    Assay Products:
     

     
    Advanced Cell Diagnostics RNAscope RNA in situ hybridization assays for SLC22A23

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

    Orthologs for SLC22A23 gene from Selected species (see all 11)    About this table
    Organism Taxonomic
    classification
    Gene Description Human
    Similarity
    Orthology
    Type
    Details
    mouse
    (Mus musculus)
    Mammalia Slc22a231 , 5 solute carrier family 22, member 231, 5 89.18(n)1
    92.51(a)1
      13 (14.05 cM)5
    731021  NM_001033167.31  NP_001028339.11 
     341791585 
    chicken
    (Gallus gallus)
    Aves SLC22A231 solute carrier family 22, member 23 79.16(n)
    81.89(a)
      420881  XM_418968.4  XP_418968.3 
    lizard
    (Anolis carolinensis)
    Reptilia --
    --
    --
    62(a)
    59(a)
    1 ↔ many
    1 ↔ many
    GL344288.1(16254-43885)
    GL343247.1(1132804-1250195)
    tropical clawed frog
    (Xenopus tropicalis)
    Amphibia slc22a231 solute carrier family 22, member 23 68.41(n)
    73.38(a)
      100491610  XM_002936427.2  XP_002936473.1 
    zebrafish
    (Danio rerio)
    Actinopterygii SLC22A23 (2 of 3)6
    SLC22A23 (3 of 3)6
    (see all 3)
    solute carrier family 22, member 23
    (see all 3)
    60(a)
    47(a)
    (see all 3)
    1 ↔ many
    1 ↔ many
    (see all 3)
    20(53322080-53328383) ENSDARG00000079638
    20(53373636-53389790) ENSDARG00000089696


    ENSEMBL Gene Tree for SLC22A23 (if available)
    TreeFam Gene Tree for SLC22A23 (if available)

    (Paralogs according to 1HomoloGene,
    2Ensembl, and 3SIMAP, Pseudogenes according to 4Pseudogene.org Build 68)
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    Paralogs for SLC22A23 gene
    SLC22A172  SLC22A312  
    4 SIMAP similar genes for SLC22A23 using alignment to 6 protein entries:     S22AN_HUMAN (see all proteins):
    DKFZp434F011    SLC22A10    SLC22A17    SLC22A31

    Find genes that share paralogs with SLC22A23           About GenesLikeMe



    (SNPs/Variants according to the 1NCBI SNP Database, 2Ensembl, 3PupaSUITE, 4UniProtKB, and DNA2.0, Linkage Disequilibrium by HapMap, Structural Variations(CNVs/InDels/Inversions) from the Database of Genomic Variants, Mutations from the Human Gene Mutation Database (HGMD), the Human Cytochrome P450 Allele Nomenclature Database, and the Locus Specific Mutation Databases (LSDB), Blood group antigen gene mutations by BGMUT, Resequencing Primers, Cancer Mutation PCR Arrays and Assays, and Copy Number PCR Arrays from QIAGEN)
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    Selected SNPs for SLC22A23 (see all 4329)    About this table                                 

    Genomic DataTranscription Related DataAllele Frequencies
    SNP IDValidClinical
    significance
    Chr 6 posSequence#AA
    Chg
    TypeMore#Allele
    freq
    PopTotal
    sample
    More
    ----------
    rs1491328881,2
    C--3268898(+) GTGCA-/GGGCAA 2 -- int10--------
    rs1473651991,2
    --3268957(+) AACCCG/TTTTTG 2 -- int10--------
    rs1394096091,2
    --3269021(+) GTGACC/GCTGGC 2 -- int10--------
    rs1819610721,2
    --3269096(+) TTCCCA/GTGCTA 2 -- int10--------
    rs65969621,2
    C,F,A,H--3269147(+) TGAGTA/GGACAC 2 -- int111Minor allele frequency- G:0.19NA WA CSA EA 374
    rs1862963811,2
    --3269247(+) TTTTCA/GTTAAA 2 -- ut310--------
    rs1998324431,2
    C--3269409(+) TGATGC/GCCCCC 2 -- ut310--------
    rs1898952661,2
    --3269512(+) CAGAGA/TGAGAG 2 -- ut310--------
    rs755097751,2
    C--3269835(+) GCACCG/ATCAGA 2 -- ut311Minor allele frequency- A:0.01NA 120
    rs3776698801,2
    C--3269895(+) GGACA-/AGGGGAG 2 -- ut310--------

    HapMap Linkage Disequilibrium report for SLC22A23 (3269196 - 3457256 bp)

    Structural Variations
         Database of Genomic Variants (DGV) Selected variations for SLC22A23 (see all 11):    About this table    
    Variant IDTypeSubtypePubMed ID
    esv2669587CNV Deletion23128226
    esv2731492CNV Deletion23290073
    esv2678916CNV Deletion23128226
    esv2731493CNV Deletion23290073
    esv2731494CNV Deletion23290073
    esv2731491CNV Deletion23290073
    esv2167684CNV Deletion18987734
    esv2461941CNV Insertion19546169
    nsv883410CNV Loss21882294
    dgv6430n71CNV Loss21882294

    Site Specific Mutation Identification with PCR Assays
    SeqTarget long-range PCR primers for resequencing SLC22A23
    DNA2.0 Custom Variant and Variant Library Synthesis for SLC22A23

    (in which this Gene is Involved, According to MalaCards, OMIM, UniProtKB, the University of Copenhagen DISEASES database, Genatlas, GeneTests, GAD, HuGE Navigator, and/or TGDB.)
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    OMIM gene information: 611697    OMIM disorders: --

    1 disease from the University of Copenhagen DISEASES database for SLC22A23:
    Wolf-Hirschhorn syndrome

    Find genes that share disorders with SLC22A23           About GenesLikeMe

    Genetic Association Database (GAD): SLC22A23
    Human Genome Epidemiology (HuGE) Navigator: SLC22A23 (9 documents)

    Export disorders for SLC22A23 gene to outside databases

    (in PubMed. Associations of this gene to articles via 1Entrez Gene, 2UniProtKB/Swiss-Prot, 3HGNC, 4GAD, 5PharmGKB, 6HMDB, 7DrugBank, 8UniProtKB/TrEMBL, 9 Novoseek, and/or 10fRNAdb)
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    PubMed articles for SLC22A23 gene, integrated from 10 sources (see all 18):
    (articles sorted by number of sources associating them with SLC22A23)
        Utopia: connect your pdf to the dynamic
    world of online information

    1. Identification of six putative human transporters with structural similarity to the drug transporter SLC22 family. (PubMed id 17714910)1, 2, 3 Jacobsson J.A.... Fredriksson R. (Genomics 2007)
    2. Genome-wide association study of antipsychotic-induced QTc interval prolongation. (PubMed id 20921969)1, 4 Aberg K....van den Oord E.J. (Pharmacogenomics J. 2012)
    3. Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score. (PubMed id 20379614)1, 4 Rose J.E....Uhl G.R. (Mol. Med. 2010)
    4. Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci. (PubMed id 21102463)1, 4 Franke A....Parkes M. (Nat. Genet. 2010)
    5. Analysis of 39 Crohn's disease risk loci in Swedish inflammatory bowel disease patients. (PubMed id 19760754)1, 4 TAPrkvist L....Pettersson S. (Inflamm. Bowel Dis. 2010)
    6. Molecular reclassification of Crohn's disease by cluster analysis of genetic variants. (PubMed id 20886065)1, 4 Cleynen I....Vermeire S. (PLoS ONE 2010)
    7. Genetic risk profiling and prediction of disease course in Crohn's disease patients. (PubMed id 19422935)1, 4 Henckaerts L....Vermeire S. (Clin. Gastroenterol. Hepatol. 2009)
    8. Confirmation of multiple Crohn's disease susceptibility loci in a large Dutch-Belgian cohort. (PubMed id 19174780)1, 4 Weersma R.K.... Vermeire S. (Am. J. Gastroenterol. 2009)
    9. Investigation of Crohn's disease risk loci in ulcerative colitis further defines their molecular relationship. (PubMed id 19068216)1, 4 Anderson C.A....Parkes M. (Gastroenterology 2009)
    10. Novel genetic loci identified for the pathophysiology of childhood obesity in the Hispanic population. (PubMed id 23251661)1 Comuzzie A.G....Butte N.F. (PLoS ONE 2012)

    (in PubMed, OMIM, and NCBI Bookshelf)
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     ANDOR
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    Free Text  

      Query String
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    OMIM
    NCBI Bookshelf
      (Note: In FireFox, select the above section and copy using Ctrl-C)

    (According to Entrez Gene, HGNC, AceView, euGenes, Ensembl, miRBase, ECgene, Kegg, and/or H-InvDB)
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    Entrez Gene: 63027 HGNC: 21106 AceView: C6orf85 Ensembl:ENSG00000137266 euGenes: HUgn63027
    ECgene: SLC22A23 H-InvDB: SLC22A23

    (According to HUGE)
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    (According to PharmGKB, ATLAS, HORDE, IMGT, LEIDEN, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL, and/or others, e.g. Wikipedia and GeneReviews, via UniProtKB/Swiss-Prot)
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    NameDescription
    PharmGKB entry for SLC22A23 Pharmacogenomics, SNPs, Pathways

    (Patent information from GeneIP,
    Licensable technologies from WIS Yeda, Salk, Tufts,
    IP news from LifeMap Sciences, Inc.)
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    Patent Information for SLC22A23 gene:
    Search GeneIP for patents involving SLC22A23

    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, Novus Biologicals, Sino Biological, Enzo Life Sciences, Abcam, ProSpec, Cloud-Clone Corp., Thermo Fisher Scientific, eBioscience, antibodies-online, and/or others, Gene Editing from DNA2.0. Clones from OriGene, GenScript, Sino Biological, DNA2.0, SwitchGear Genomics, Vector BioLabs, Addgene, Cell lines from GenScript, and ESI BIO, Flow cytometery from eBioscience, PCR Arrays from QIAGEN, Drugs and/or compounds from EMD Millipore, Tocris Bioscience, Enzo Life Sciences, and/or ApexBio, In Situ Hybridization Assays from
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