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SLC2A13 Gene

protein-coding   GIFtS: 56
GCID: GC12M040152

Solute Carrier Family 2 (Facilitated Glucose Transporter),...

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at  

(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 2 (Facilitated Glucose Transporter), Member
131 2
     HMIT2 5
H(+)-Myo-Inositol Symporter1 2 3     Proton (H+) Myo-Inositol Symporter2
H(+)-Myo-Inositol Cotransporter2 3     Proton Myo-Inositol Cotransporter2
Solute Carrier Family 2 Member 132 3     Hmit3

External Ids:    HGNC: 159561   Entrez Gene: 1141342   Ensembl: ENSG000001512297   OMIM: 6110365   UniProtKB: Q96QE23   

Export aliases for SLC2A13 gene to outside databases

Previous GC identifers: GC12M040312 GC12M040051 GC12M039869 GC12M038438 GC12M037175


(According to Entrez Gene, GeneCards, Tocris Bioscience, Wikipedia's Gene Wiki, PharmGKB,
UniProtKB/Swiss-Prot, and/or UniProtKB/TrEMBL)
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GeneCards Summary for SLC2A13 Gene:
SLC2A13 (solute carrier family 2 (facilitated glucose transporter), member 13) is a protein-coding gene. GO annotations related to this gene include substrate-specific transmembrane transporter activity. An important paralog of this gene is SLC2A10.

UniProtKB/Swiss-Prot: MYCT_HUMAN, Q96QE2
Function: H(+)-myo-inositol cotransporter. Can also transport related stereoisomers

Gene Wiki entry for SLC2A13 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 75), Regulatory elements and Epigenetics data according to QIAGEN, and/or SwitchGear Genomics)
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RefSeq DNA sequence:
NC_000012.12  NT_029419.13  NC_018923.2  
Regulatory elements:
   Regulatory transcription factor binding sites in the SLC2A13 gene promoter:
         AhR   Elk-1   Pax-5   Pbx1a   NRSF form 1   CUTL1   NRSF form 2   FOXO1a   STAT3   FOXO1   
         Other transcription factors

SwitchGear Promoter luciferase reporter plasmidSLC2A13 promoter sequence
   Search Chromatin IP Primers for SLC2A13

Epigenetics:
DNA Methylation CpG Assay Predesigned for Pyrosequencing in human, mouse, rat SLC2A13


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

Entrez Gene cytogenetic band: 12q12   Ensembl cytogenetic band:  12q12   HGNC cytogenetic band: 12q12

SLC2A13 Gene in genomic location: bands according to Ensembl, locations according to (and/or Entrez Gene and/or Ensembl if different)
SLC2A13 gene location

GeneLoc information about chromosome 12         GeneLoc Exon Structure

GeneLoc location for GC12M040152:  view genomic region     (about GC identifiers)

Start:
40,148,823 bp from pter      End:
40,499,891 bp from pter
Size:
351,069 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., and/or eBioscience,
Biochemical Assays by EMD Millipore, R&D Systems, OriGene, GenScript, Cell Signaling Technology, Enzo Life Sciences, Cloud-Clone Corp., and/or eBioscience, Antibodies by EMD Millipore, R&D Systems, Cell Signaling Technology, OriGene, Novus Biologicals, Thermo Fisher Scientific, LSBio, Abcam, Cloud-Clone Corp, and/or others.)
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UniProtKB/Swiss-Prot: MYCT_HUMAN, Q96QE2 (See protein sequence)
Recommended Name: Proton myo-inositol cotransporter  
Size: 648 amino acids; 70371 Da
Sequence caution: Sequence=AAI17118.1; Type=Erroneous initiation; Note=Translation N-terminally extended;
Sequence=AAI17120.1; Type=Erroneous initiation; Note=Translation N-terminally extended; Sequence=CAC51116.1;
Type=Erroneous initiation; Note=Translation N-terminally extended;
Secondary accessions: Q17S07

Explore the universe of human proteins at neXtProt for SLC2A13: NX_Q96QE2

Explore proteomics data for SLC2A13 at MOPED

Post-translational modifications: 

  • Glycosylated1
  • Glycosylation2 at Asn433, Asn458, Asn485
  • Modification sites at PhosphoSitePlus

  • See SLC2A13 Protein Expression from SPIRE MOPED, PaxDB, and MaxQB

    REFSEQ proteins: NP_443117.3  
    ENSEMBL proteins: 
     ENSP00000280871   ENSP00000370239  
    Reactome Protein details: Q96QE2

    SLC2A13 Human Recombinant Protein Products:

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    Novus Biologicals SLC2A13 Lysates
    Browse Sino Biological Recombinant Proteins
    Browse Sino Biological Cell Lysates
    Browse ProSpec Recombinant Proteins
    Browse Proteins at Cloud-Clone Corp.

     
    Search eBioscience for Proteins for SLC2A13 

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    Search eBioscience for ELISAs for SLC2A13 


    (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: Proton myo-inositol cotransporter
    Proton-coupled inositol transporter

    5 InterPro protein domains:
     IPR005829 Sugar_transporter_CS
     IPR005828 Sub_transporter
     IPR003663 Sugar/inositol_transpt
     IPR020846 MFS_dom
     IPR016196 MFS_dom_general_subst_transpt

    Graphical View of Domain Structure for InterPro Entry Q96QE2

    ProtoNet protein and cluster: Q96QE2

    2 Blocks protein domains:
    IPB003663 Sugar transporter signature
    IPB005829 Sugar transporter superfamily


    UniProtKB/Swiss-Prot: MYCT_HUMAN, Q96QE2
    Similarity: Belongs to the major facilitator superfamily. Sugar transporter (TC 2.A.1.1) family


    Find genes that share domains with SLC2A13           About GenesLikeMe


    (According to 1UniProtKB, Genatlas, LifeMap Discovery™, IUBMB, and/or 2DME, Human phenotypes from GenomeRNAi, Animal models from MGI Mar 06 2013, inGenious Targeting Laboratory, genOway,
    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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    Molecular Function:

         UniProtKB/Swiss-Prot Summary: MYCT_HUMAN, Q96QE2
    Function: H(+)-myo-inositol cotransporter. Can also transport related stereoisomers

         Gene Ontology (GO): 3 molecular function terms:    About this table

    GO IDQualified GO termEvidencePubMed IDs
    GO:0004872receptor activity ----
    GO:0022857transmembrane transporter activity ----
    GO:0022891substrate-specific transmembrane transporter activity IEA--
         
    Find genes that share ontologies with SLC2A13           About GenesLikeMe


    Phenotypes:
         1 GenomeRNAi human phenotype for SLC2A13:
     Lamellipodia and high actin ra 

    Animal Models:
       inGenious Targeting Laboratory: Let us create your new Knockout/Knockin mouse model for SLC2A13
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       genOway customized KO model: permanent, tissue-specific or time-controlled inactivation for SLC2A13
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    miRNA
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    miRTarBase miRNAs that target SLC2A13:
    hsa-mir-335-5p (MIRT019106)

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    Selected qRT-PCR Assays for microRNAs that regulate SLC2A13 (see all 61):
    hsa-miR-411* hsa-miR-579 hsa-miR-142-5p hsa-miR-4307 hsa-miR-379* hsa-miR-300 hsa-miR-449a hsa-miR-570
    Browse SwitchGear 3'UTR luciferase reporter plasmids
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    Advanced Cell Diagnostics RNAscope RNA in situ hybridization assays for SLC2A13


    (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
    MYCT_HUMAN, Q96QE2: Membrane; Multi-pass membrane protein
    Subcellular locations from COMPARTMENTS: 

    CompartmentConfidence
    plasma membrane4
    peroxisome2

    Gene Ontology (GO): 3 cellular component terms:    About this table

    GO IDQualified GO termEvidencePubMed IDs
    GO:0005886plasma membrane TAS--
    GO:0016020membrane ----
    GO:0016021integral component of membrane IEA--

    Find genes that share ontologies with SLC2A13           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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    SuperPaths for SLC2A13 About    
    See pathways by source

    SuperPathContained pathways About
    1Transport of glucose and other sugars, bile salts and organic acids, metal ions and amine compounds
    SLC-mediated transmembrane transport0.47
    Transport of glucose and other sugars, bile salts and organic acids, metal ions and amine compounds0.38
    Transmembrane transport of small molecules0.47
    Inositol transporters0.00


    Find genes that share SuperPaths with SLC2A13           About GenesLikeMe

    Pathways by source                                                                                                                                                                 See SuperPaths
    Show all pathways


    1 Reactome Pathway for SLC2A13
        Inositol transporters


        Custom Pathway & Disease-focused RT2 Profiler PCR Arrays for SLC2A13
    Interactions:

        Search GeneGlobe Interaction Network for SLC2A13

    STRING Interaction Network Preview (showing 4 interactants - click image to see more details)

    Selected Interacting proteins for SLC2A13 (Q96QE23 ENSP000002808714) via UniProtKB, MINT, STRING, and/or I2D (see all 15)
    InteractantInteraction Details
    GeneCardExternal ID(s)
    AK2P548193I2D: score=1 
    CADP277083I2D: score=1 
    CBSP355203I2D: score=1 
    DHX8Q145623I2D: score=1 
    FPGSQ059323I2D: score=1 
    About this table

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

    GO IDQualified GO termEvidencePubMed IDs
    GO:0007275multicellular organismal development ----
    GO:0055085transmembrane transport TAS--

    Find genes that share ontologies with SLC2A13           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 SLC2A13 (MYCT)



    (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 SLC2A13 gene: 
    NM_052885.3  

    Unigene Cluster for SLC2A13:

    Solute carrier family 2 (facilitated glucose transporter), member 13
    Hs.558595  [show with all ESTs]
    Unigene Representative Sequence: NM_052885
    4 Ensembl transcripts including schematic representations, and UCSC links where relevant:
    ENST00000280871(uc010skm.2) ENST00000465517(uc001rme.1) ENST00000505338
    ENST00000380858(uc001rmf.3)
    miRNA
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    Block miRNA regulation of human, mouse, rat SLC2A13 using miScript Target Protectors
    Selected qRT-PCR Assays for microRNAs that regulate SLC2A13 (see all 61):
    hsa-miR-411* hsa-miR-579 hsa-miR-142-5p hsa-miR-4307 hsa-miR-379* hsa-miR-300 hsa-miR-449a hsa-miR-570
    Browse SwitchGear 3'UTR luciferase reporter plasmids
    Inhib. RNA
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    Predesigned siRNA for gene silencing in human, mouse, rat SLC2A13
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      QuantiTect SYBR Green Assays in human, mouse, rat SLC2A13
      QuantiFast Probe-based Assays in human, mouse, rat SLC2A13

    Additional mRNA sequence: 

    AJ315644.1 AK000182.1 AK026495.1 BC039431.1 BC047507.1 BC117117.1 BC117119.1 

    3 DOTS entries:

    DT.444219  DT.100738505  DT.91966328 

    Selected AceView cDNA sequences (see all 35):

    CD635364 BX110008 AL120094 CD635348 AL700130 NM_052885 CD635366 BX492538 
    CD635356 BM995856 BX486694 CD635360 AA644240 AK000182 AL603403 BX497350 
    AJ315644 CD635358 BC047507 CD635350 BX493371 AI168212 CD635352 H99108 

    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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    SLC2A13 expression in normal human tissues (normalized intensities)
    See probesets specificity/sensitivity at GeneAnnot
    About this imageBioGPS <intensity>2/3
    CGAP TAG: --
    SLC2A13 Expression
    About this image


    SLC2A13 expression in embryonic tissues and stem cells    About this table
    Data from LifeMap, the Embryonic Development and Stem Cells Database
     selected tissues (see all 3) fully expand
     
     Heart (Cardiovascular System)
             Endocardial Tube Cells Endocardium
     
     Neurons
             nGnG Amacrine Cells Inner Nuclear Layer
     
     Eye (Sensory Organs)
             nGnG Amacrine Cells Inner Nuclear Layer
    SLC2A13 Protein expression data from MOPED1, PaxDb2 and MaxQB3    About this image

    SLC2A13 Protein Expression

    SOURCE GeneReport for Unigene cluster: Hs.558595

    UniProtKB/Swiss-Prot: MYCT_HUMAN, Q96QE2
    Tissue specificity: Predominantly expressed in the brain

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    In Situ
    Assay Products:
     

     
    Advanced Cell Diagnostics RNAscope RNA in situ hybridization assays for SLC2A13

    (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 eukaryotes.

    Orthologs for SLC2A13 gene from Selected species (see all 20)    About this table
    Organism Taxonomic
    classification
    Gene Description Human
    Similarity
    Orthology
    Type
    Details
    mouse
    (Mus musculus)
    Mammalia Slc2a131 , 5 solute carrier family 2 (facilitated glucose transporter), more1, 5 85.4(n)1
    89.95(a)1
      15 (46.05 cM)5
    2396061  NM_001033633.31  NP_001028805.21 
     912676965 
    chicken
    (Gallus gallus)
    Aves SLC2A131 solute carrier family 2 (facilitated glucose transporter), more 81.7(n)
    86.31(a)
      769652  XM_001232939.3  XP_001232940.2 
    lizard
    (Anolis carolinensis)
    Reptilia SLC2A136
    solute carrier family 2 (facilitated glucose trans...
    86(a)
    1 ↔ 1
    5(98376346-98513767)
    tropical clawed frog
    (Xenopus tropicalis)
    Amphibia slc2a131 solute carrier family 2 (facilitated glucose transporter), more 76.07(n)
    82.79(a)
      100485871  XM_004913004.1  XP_004913061.1 
    zebrafish
    (Danio rerio)
    Actinopterygii slc2a13b1 solute carrier family 2 (facilitated glucose transporter), more 65.03(n)
    69(a)
      559440  NM_001159829.1  NP_001153301.1 
    worm
    (Caenorhabditis elegans)
    Secernentea Y51A2D.43
    hmit-1.31
    Sugar (and other) transporters3
    hmit-1.31
    39(a)
    (best of 3)3
    50.4(n)1
    44.61(a)1
      V(18519464-18526280)3
    1754581  NM_065324.31  NP_497725.21 
    baker's yeast
    (Saccharomyces cerevisiae)
    Saccharomycetes ITR2(YOL103W)4
    ITR21
    Myo-inositol transporter with strong similarity to more4
    ITR21
    47.88(n)1
    35.33(a)1
      15(124001-125830)4
    8540501, 4  NP_014538.21, 4 
    thale cress
    (Arabidopsis thaliana)
    eudicotyledons INT11 INT1 51.42(n)
    42.77(a)
      818934  NM_180062.2  NP_850393.1 
    rice
    (Oryza sativa)
    Liliopsida Os.101172 Oryza sativa (japonica cultivar-group) cDNA cloneJ more 71.98(n)    AK069132.1 


    ENSEMBL Gene Tree for SLC2A13 (if available)
    TreeFam Gene Tree for SLC2A13 (if available)

    (Paralogs according to 1HomoloGene,
    2Ensembl, and 3SIMAP, Pseudogenes according to 4Pseudogene.org Build 68)
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    Paralogs for SLC2A13 gene
    SLC2A102  SLC2A122  
    3 SIMAP similar genes for SLC2A13 using alignment to 3 protein entries:     MYCT_HUMAN (see all proteins):
    SLC2A10    SLC2A12    SLC2A14

    Find genes that share paralogs with SLC2A13           About GenesLikeMe


    1 Pseudogenes.org Pseudogene for SLC2A13
    PGOHUM00000249685


    (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 SLC2A13 (see all 6569)    About this table                                 

    Genomic DataTranscription Related DataAllele Frequencies
    SNP IDValidClinical
    significance
    Chr 12 posSequence#AA
    Chg
    TypeMore#Allele
    freq
    PopTotal
    sample
    More
    ----------
    rs779598701,2
    C--40148397(+) TGATTA/GAGGCA 1 -- int10--------
    rs790292621,2
    C--40148398(+) GATTGA/TGGCAG 1 -- int10--------
    rs1443860981,2
    --40148427(+) CGGAGC/TCCCAA 1 -- int10--------
    rs111734331,2
    C,F,A,H--40148465(+) CGATTG/TTTCAT 1 -- int123Minor allele frequency- T:0.18NS EA NA WA 2770
    rs1830102171,2
    --40148640(+) TTTTAG/TGTATT 1 -- int10--------
    rs111734341,2
    C,F,H--40148791(+) GAAGAT/AAACTA 1 -- int19Minor allele frequency- A:0.17NS EA NA WA 754
    rs1868599611,2
    --40148831(+) ATGAGC/TAATGA 1 -- ut310--------
    rs47681771,2
    H--40149094(+) ACTTAT/CATTGA 1 -- ut314Minor allele frequency- C:0.00NS EA 404
    rs111734401,2
    C,F,H--40149382(+) TAAATG/TAGATG 1 -- ut319Minor allele frequency- T:0.16NS EA NA WA 760
    rs1905488891,2
    --40149453(+) ATGATC/GCACTT 1 -- ut310--------

    HapMap Linkage Disequilibrium report for SLC2A13 (40148823 - 40398823 bp, first 250kb of SLC2A13)

    Structural Variations
         Database of Genomic Variants (DGV) Selected variations for SLC2A13 (see all 26):    About this table    
    Variant IDTypeSubtypePubMed ID
    esv2745780CNV Deletion23290073
    esv2677205CNV Deletion23128226
    esv2745781CNV Deletion23290073
    esv2745779CNV Deletion23290073
    esv2661429CNV Deletion23128226
    nsv436152CNV Deletion17901297
    esv2678856CNV Deletion23128226
    esv2421863CNV Deletion20811451
    esv2657004CNV Deletion23128226
    nsv681CNV Insertion18451855

    Site Specific Mutation Identification with 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.)
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    OMIM gene information: 611036    OMIM disorders: --


    Find genes that share disorders with SLC2A13           About GenesLikeMe

    Genetic Association Database (GAD): SLC2A13
    Human Genome Epidemiology (HuGE) Navigator: SLC2A13 (1 document)

    Export disorders for SLC2A13 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 SLC2A13 gene, integrated from 10 sources (see all 20):
    (articles sorted by number of sources associating them with SLC2A13)
        Utopia: connect your pdf to the dynamic
    world of online information

    1. Identification of a mammalian H(+)-myo-inositol symporter expressed predominantly in the brain. (PubMed id 11500374)1, 2, 3 Uldry M.... Thorens B. (EMBO J. 2001)
    2. Meta-analysis of Parkinson's disease: identification of a novel locus, RIT2. (PubMed id 22451204)1, 4 Pankratz N....Foroud T. (Ann. Neurol. 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 association study identifies common variants at four loci as genetic risk factors for Parkinson's disease. (PubMed id 19915576)1, 4 Satake W....Toda T. (Nat. Genet. 2009)
    5. Global, in vivo, and site-specific phosphorylation dynamics in signaling networks. (PubMed id 17081983)1, 2 Olsen J.V....Mann M. (Cell 2006)
    6. 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. (Genome Res. 2004)
    7. Evaluation of expression and function of the H+/myo-inositol transporter HMIT. (PubMed id 19607714)1, 9 Di Daniel E....Maycox P.R. (BMC Cell Biol. 2009)
    8. Genetics of coronary artery calcification among African Americans, a meta-analysis. (PubMed id 23870195)1 Wojczynski M.K....Reilly M.P. (BMC Med. Genet. 2013)
    9. A genome-wide association study of sleep habits and insomnia. (PubMed id 23728906)1 Byrne E.M....Wray N.R. (Am. J. Med. Genet. B Neuropsychiatr. Genet. 2013)
    10. Quantitative phosphoproteomics reveals widespread full phosphorylation site occupancy during mitosis. (PubMed id 20068231)2 Olsen J.V....Mann M. (Sci. Signal. 2010)

    (in PubMed, OMIM, and NCBI Bookshelf)
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     ANDOR
    Aliases
    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: 114134 HGNC: 15956 AceView: SLC2A13 Ensembl:ENSG00000151229 euGenes: HUgn114134
    ECgene: SLC2A13 H-InvDB: SLC2A13

    (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 SLC2A13 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 SLC2A13 gene:
    Search GeneIP for patents involving SLC2A13

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



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