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

SLC16A9 Gene

protein-coding   GIFtS: 54
GCID: GC10M061410

Solute Carrier Family 16, Member 9

(Previous names: chromosome 10 open reading frame 36, solute carrier family...)
(Previous symbol: C10orf36)
Alzheimer's & Parkinson's Diseases Congress
  See related diseases
at  

(According to 1HGNC, 2Entrez Gene,
3UniProtKB/Swiss-Prot, 4UniProtKB/TrEMBL, 5OMIM, 6GeneLoc, 7Ensembl, 8DME, 9miRBase, 10fRNAdb, 12H-InvDB, 13NCBI, 14NONCODE, and/or 15RNAdb)
About This Section

Aliases
Solute Carrier Family 16, Member 91 2     Solute Carrier Family 16 Member 92 3
C10orf361 2 3     MCT92 3
Solute Carrier Family 16 (Monocarboxylic Acid Transporters), Member 91 2     MCT 92 3
Solute Carrier Family 16, Member 9 (Monocarboxylic Acid Transporter 9)1 2     Chromosome 10 Open Reading Frame 361
Monocarboxylic Acid Transporter 91 2     Monocarboxylate Transporter 92

External Ids:    HGNC: 235201   Entrez Gene: 2209632   Ensembl: ENSG000001654497   OMIM: 6142425   UniProtKB: Q7RTY13   

Export aliases for SLC16A9 gene to outside databases

Previous GC identifers: GC10M060757 GC10M060755 GC10M061080 GC10M055397


(According to Entrez Gene, Tocris Bioscience, Wikipedia's Gene Wiki, PharmGKB,
UniProtKB/Swiss-Prot, and/or UniProtKB/TrEMBL)
About This Section

GeneCards Summary for SLC16A9 Gene: 
SLC16A9 (solute carrier family 16, member 9) is a protein-coding gene. Diseases associated with SLC16A9 include hyperuricemia, and gout. GO annotations related to this gene include symporter activity. An important paralog of this gene is SLC16A4.

UniProtKB/Swiss-Prot: MOT9_HUMAN, Q7RTY1
Function: Proton-linked monocarboxylate transporter. Catalyzes the rapid transport across the plasma membrane of
many monocarboxylates (By similarity)

Gene Wiki entry for SLC16A9 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 73), Regulatory elements and Epigenetics data according to QIAGEN, SABiosciences, and/or SwitchGear Genomics)
About This Section
RefSeq DNA sequence:
NC_000010.10  NC_018921.2  NT_030059.13  
Regulatory elements:
   SABiosciences Regulatory transcription factor binding sites in the SLC16A9 gene promoter:
         TBP   NF-AT   HNF-1A   MEF-2A   NF-AT4   NF-AT2   HNF-1   c-Myb   NF-AT3   NF-AT1   
         Other transcription factors

SwitchGear Promoter luciferase reporter plasmids (see all 3): SLC16A9 promoter sequence
   Search SABiosciences Chromatin IP Primers for SLC16A9

Epigenetics:
QIAGEN PyroMark CpG Assay predesigned Pyrosequencing DNA Methylation assays in human, mouse, rat SLC16A9


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

Entrez Gene cytogenetic band: 10q21.2   Ensembl cytogenetic band:  10q21.2   HGNC cytogenetic band: 10q21.3

SLC16A9 Gene in genomic location: bands according to Ensembl, locations according to (and/or Entrez Gene and/or Ensembl if different)
SLC16A9 gene location

GeneLoc information about chromosome 10         GeneLoc Exon Structure

GeneLoc location for GC10M061410:  view genomic region     (about GC identifiers)

Start:
61,410,522 bp from pter      End:
61,495,760 bp from pter
Size:
85,239 bases      Orientation:
minus strand

(According to UniProtKB, HORDE, neXtProt, Ensembl, and/or Reactome, Modification sites according to PhosphoSitePlus, Specific Peptides from DME, Protein expression images according to data from SPIRE 1MOPED, 2PaxDb, and 3MAXQB 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 Cloud-Clone Corp.,
Biochemical Assays by EMD Millipore, R&D Systems, OriGene, GenScript, Cell Signaling Technology, Enzo Life Sciences, and/or Cloud-Clone Corp., Ontologies according to Gene Ontology Consortium 01 Oct 2013 and Entrez Gene, Antibodies by EMD Millipore, R&D Systems, GenScript, Cell Signaling Technology, OriGene, Novus Biologicals, Thermo Fisher Scientific, LSBio, Abcam, and/or Cloud-Clone Corp.)
About This Section

UniProtKB/Swiss-Prot: MOT9_HUMAN, Q7RTY1 (See protein sequence)
Recommended Name: Monocarboxylate transporter 9  
Size: 509 amino acids; 55794 Da
Subcellular location: Cell membrane; Multi-pass membrane protein (By similarity)
Sequence caution: Sequence=BAD18743.1; Type=Erroneous initiation;
Secondary accessions: Q6ZMI2 Q9UFH8

Explore the universe of human proteins at neXtProt for SLC16A9: NX_Q7RTY1

Post-translational modifications:

  • View modification sites using PhosphoSitePlus
  • View neXtProt modification sites for NX_Q7RTY1

  • SLC16A9 Protein expression data from MOPED1, PaxDb2 and MAXQB3 : --
    REFSEQ proteins: NP_919274.1  
    ENSEMBL proteins: 
     ENSP00000378757   ENSP00000378756  

    Human Recombinant Protein Products for SLC16A9: 
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    Cloud-Clone Corp. Proteins for SLC16A9 

    Gene Ontology (GO): 2 cellular component terms (GO ID links to tree view):    About this table

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

    SLC16A9 for ontologies           About GeneDecksing



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

    IUPHAR Guide to PHARMACOLOGY protein family classification: Monocarboxylate transporter 9 
    SLC16 family of monocarboxylate transporters

    3 InterPro protein domains:
     IPR020846 MFS_dom
     IPR011701 MFS
     IPR016196 MFS_dom_general_subst_transpt

    Graphical View of Domain Structure for InterPro Entry Q7RTY1

    ProtoNet protein and cluster: Q7RTY1

    UniProtKB/Swiss-Prot: MOT9_HUMAN, Q7RTY1
    Similarity: Belongs to the major facilitator superfamily. Monocarboxylate porter (TC 2.A.1.13) family


    SLC16A9 for domains           About GeneDecksing


    (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,
    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, Sirion Biotech, Clones from EMD Millipore, OriGene, SwitchGear Genomics, GenScript, Sino Biological, DNA2.0, Vector BioLabs, and Sirion Biotech, Cell Lines from GenScript, LifeMap BioReagents, In Situ Hybridization Assays from Advanced Cell Diagnostics, Ontologies according to Gene Ontology Consortium 01 Oct 2013 via Entrez Gene.)
    About This Section

    Molecular Function:

         UniProtKB/Swiss-Prot Summary: MOT9_HUMAN, Q7RTY1
    Function: Proton-linked monocarboxylate transporter. Catalyzes the rapid transport across the plasma membrane of
    many monocarboxylates (By similarity)

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

    GO IDQualified GO termEvidencePubMed IDs
    GO:0015293symporter activity IEA--
         
    SLC16A9 for ontologies           About GeneDecksing


    Animal Models:
       inGenious Targeting Laboratory - Custom generated mouse model solutions for SLC16A9 
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    miRNA
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    miRTarBase miRNAs that target SLC16A9:
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    QIAGEN Custom miScript Target Protector blocks miRNA-binding site of human, mouse, rat SLC16A9
    8/49 QIAGEN miScript miRNA Assays for microRNAs that regulate SLC16A9 (see all 49):
    hsa-miR-142-5p hsa-miR-520e hsa-miR-302d hsa-miR-520f hsa-miR-607 hsa-let-7d hsa-miR-106a hsa-miR-4305
    SwitchGear 3'UTR luciferase reporter plasmidSLC16A9 3' UTR sequence
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    Advanced Cell Diagnostics RNAscope RNA in situ hybridization assays for SLC16A9


    (Pathways according to EMD Millipore, 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 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 Oct 2013 via Entrez Gene).
    About This Section



    Interactions:

        Search SABiosciences Gene Network CentralTM Interacting Genes and Proteins Networks for SLC16A9

    Gene Ontology (GO): 2 biological process terms (GO ID links to tree view):    About this table

    GO IDQualified GO termEvidencePubMed IDs
    GO:0046415urate metabolic process IMP19503597
    GO:0055085transmembrane transport ----

    SLC16A9 for ontologies           About GeneDecksing



    (Chemical Compounds according to UniProtKB, Enzo Life Sciences, EMD Millipore, Tocris Bioscience HMDB, BitterDB, and/or Novoseek, Ligands according to IUPHAR, 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 SLC16A9 (MOT9)

    Search CenterWatch for drugs/clinical trials and news about SLC16A9 / MOT9

    (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,
    Conferences by KenesGroup, 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, Sirion Biotech, Primers from OriGene, SABiosciences, and/or QIAGEN )
    About This Section

    REFSEQ mRNAs for SLC16A9 gene: 
    NM_194298.2  

    Unigene Cluster for SLC16A9:

    Solute carrier family 16, member 9 (monocarboxylic acid transporter 9)
    Hs.499709  [show with all ESTs]
    Unigene Representative Sequence: AK126643
    3 Ensembl transcripts including schematic representations, and UCSC links where relevant:
    ENST00000395348(uc010qig.1) ENST00000395347 ENST00000490066

    miRNA
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    8/49 QIAGEN miScript miRNA Assays for microRNAs that regulate SLC16A9 (see all 49):
    hsa-miR-142-5p hsa-miR-520e hsa-miR-302d hsa-miR-520f hsa-miR-607 hsa-let-7d hsa-miR-106a hsa-miR-4305
    SwitchGear 3'UTR luciferase reporter plasmidSLC16A9 3' UTR sequence
    Inhib. RNA
    Products:
         
    Browse for Gene Knock-down Tools from EMD Millipore
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      QIAGEN QuantiFast Probe-based Assays in human, mouse, rat SLC16A9

    Additional mRNA sequence: 

    AK021827.1 AK125791.1 AK126643.1 AK172758.1 AL122071.1 BC126238.1 BC130567.1 

    6 DOTS entries:

    DT.313023  DT.91994302  DT.109363  DT.40242868  DT.86841491  DT.121288486 

    24/68 AceView cDNA sequences (see all 68):

    AI335791 CB215396 AW025596 AA918397 AA301375 AA680268 BX092606 AK125791 
    NM_194298 AI050785 BN000144 AI075056 BM699331 AA931188 AA862478 N73702 
    AI272128 BQ708996 AW611820 W39215 AK021827 BX952245 AA657542 N78548 

    GeneLoc Exon Structure

    5/6 Alternative Splicing Database (ASD) splice patterns (SP) for SLC16A9 (see all 6)    About this scheme

    ExUns: 1 ^ 2a · 2b ^ 3 ^ 4 ^ 5 ^ 6a · 6b ^ 7a · 7b ^ 8 ^ 9a · 9b · 9c ^ 10a · 10b
    SP1:        -     -     -     -     -                                               -               
    SP2:                    -     -     -                                                               
    SP3:                    -           -                                                               
    SP4:                                                                                                
    SP5:                          -     -                                                               


    ECgene alternative splicing isoforms for SLC16A9

    (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

    SLC16A9 expression in normal human tissues (normalized intensities)      SLC16A9 embryonic expression: see
    See probesets specificity/sensitivity at GeneAnnot
    About this imageBioGPS <intensity>2/3
    CGAP TAG: GGATATGGGA
    SLC16A9 Expression
    About this image


    SLC16A9 expression in embryonic tissues and stem cells    About this table
    Data from LifeMap, the Embryonic Development and Stem Cells Database 
     5/14 selected tissues (see all 14) fully expand
     
     Brain (Nervous System)    fully expand to see all 5 entries
             Endothelial Cells Blood Brain Barrier
             Medulla Oblongata
             brain/forebrain/telencephalon   
     
     Bone (Muscoskeletal System)    fully expand to see all 3 entries
             HyStem+BMP4-induced MEL2 cells
     
     Cartilage (Muscoskeletal System)    fully expand to see all 2 entries
             HyStem+BMP4-induced E15 cells
     
     Adipose (Muscoskeletal System)    fully expand to see all 2 entries
             HyStem+BMP4-induced E15 cells
     
     Blood (Hematopoietic System)    fully expand to see all 2 entries
             Hematopoietic Stem Cells Hematopoietic Bone Marrow

    Genevestigator expression for SLC16A9

    SOURCE GeneReport for Unigene cluster: Hs.499709
        SABiosciences Custom PCR Arrays for SLC16A9
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    In Situ
    Assay Products:
     

     
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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 SLC16A9 gene from 6/12 species (see all 12)    About this table
    Organism Taxonomic
    classification
    Gene Description Human
    Similarity
    Orthology
    Type
    Details
    mouse
    (Mus musculus)
    Mammalia Slc16a91 , 5 solute carrier family 16 (monocarboxylic acid transporters), more1, 5 82.61(n)1
    88.34(a)1
      10 (36.68 cM)5
    668591  NM_025807.31  NP_080083.21 
     702451005 
    chicken
    (Gallus gallus)
    Aves SLC16A91 solute carrier family 16, member 9 (monocarboxylic more 76.96(n)
    79.21(a)
      423667  NM_001031222.1  NP_001026393.1 
    lizard
    (Anolis carolinensis)
    Reptilia SLC16A96
    --
    Uncharacterized protein
    74(a)
    26(a)
    1 ↔ 1
    possible ortholog
    GL343251.1(391754-427843)
    1(225466406-225473739)
    African clawed frog
    (Xenopus laevis)
    Amphibia BJ095133.12   -- 74.35(n)    BJ095133.1 
    zebrafish
    (Danio rerio)
    Actinopterygii BC054615.12   -- 74.01(n)   393382  BC054615.1 
    mosquito
    (Anopheles gambiae)
    Insecta AgaP_AGAP0017821 AGAP001782-PA 45.95(n)
    39.55(a)
      1281333  XM_321287.4  XP_321287.4 


    ENSEMBL Gene Tree for SLC16A9 (if available)
    TreeFam Gene Tree for SLC16A9 (if available)

    (Paralogs according to 1HomoloGene,
    2Ensembl, and 3SIMAP, Pseudogenes according to 4Pseudogene.org Build 68)
    About This Section
    Paralogs for SLC16A9 gene
    SLC16A42  SLC16A32  SLC16A102  SLC16A52  SLC16A112  SLC16A22  SLC16A62  SLC16A82  
    SLC16A142  SLC16A72  SLC16A12  SLC16A122  SLC16A132  
    4 SIMAP similar genes for SLC16A9 using alignment to 1 protein entry:     MOT9_HUMAN:
    SLC16A14    SLC16A7    SLC16A10    SLC16A4

    SLC16A9 for paralogs           About GeneDecksing



    (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) 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

    10/1416 SNPs in SLC16A9 are shown (see all 1416)    About this table     
    Genomic DataTranscription Related DataAllele Frequencies
    SNP IDValidClinical
    significance
    Chr 10 posSequence#AA
    Chg
    TypeMore#Allele
    freq
    PopTotal
    sample
    More
    ----------
    rs122488311,2
    C,F,A,H--61410064(+) CCAGGG/CCTAAT 1 -- int15Minor allele frequency- C:0.05NS EA WA 528
    rs108263381,2
    C,F,A,H--61410115(+) CTACAA/GAGAGA 1 -- int19Minor allele frequency- G:0.26NA WA EA 372
    rs70686051,2
    C,F,H--61410247(+) TATGAA/C/GGGTTA 1 -- int113NA NS EA WA CSA 920
    rs1421716471,2
    --61410271(+) TGAAAC/TATATT 1 -- int10--------
    rs122641401,2
    F,A,H--61410304(+) AAGAAC/TTAAGA 1 -- int15Minor allele frequency- T:0.03NS EA WA 514
    rs1507592031,2
    --61410450(+) ATTTAC/TAGTTT 1 -- int10--------
    rs775751191,2
    C,F--61410466(+) TCAAGT/CGACAT 1 -- int11Minor allele frequency- C:0.12WA 118
    rs1391185081,2
    --61410524(+) TGATGA/CAAAAC 1 -- ut310--------
    rs1904479591,2
    --61410647(+) TTGATG/TAATAT 1 -- ut310--------
    rs770310381,2
    C,F--61410697(+) GGTTTC/TCTGAA 1 -- ut311Minor allele frequency- T:0.12WA 118

    HapMap Linkage Disequilibrium report for SLC16A9 (61410522 - 61495760 bp)

    Structural Variations
         Database of Genomic Variants (DGV) 6 variations for SLC16A9:    About this table     
    Variant IDTypeSubtypePubMed ID
    esv2737462CNV Deletion23290073
    esv2613224CNV Deletion19546169
    esv2674517CNV Deletion23128226
    esv1583704CNV Deletion17803354
    nsv825405CNV Loss20364138
    nsv819969CNV Loss19587683

    SABiosciences Cancer Mutation PCR Assays
    SeqTarget long-range PCR primers for resequencing SLC16A9
    DNA2.0 Custom Variant and Variant Library Synthesis for SLC16A9

    (in which this Gene is Involved, According to MalaCards, OMIM, UniProtKB, the University of Copenhagen DISEASES database, Conferences by KenesGroup, Genatlas, GeneTests, GAD, HuGE Navigator, and/or TGDB.)
    About This Section
    OMIM gene information: 614242    OMIM disorders: --

    3 diseases for SLC16A9:    About MalaCards
    hyperuricemia    gout    alzheimer's disease

    2 diseases from the University of Copenhagen DISEASES database for SLC16A9:
    Gout     Hyperuricemia

    SLC16A9 for disorders           About GeneDecksing


    Congresses - knowledge worth sharing:  
    Alzheimer's & Parkinson's Diseases Congress (ADPD) 18 - 22 March 2015
    Genetic Association Database (GAD): SLC16A9
    Human Genome Epidemiology (HuGE) Navigator: SLC16A9 (8 documents)

    Export disorders for SLC16A9 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 SLC16A9 gene, integrated from 9 sources (see all 19):
    (articles sorted by number of sources associating them with SLC16A9)
        Utopia: connect your pdf to the dynamic
    world of online information

    1. Human metabolic individuality in biomedical and pharma ceutical research. (PubMed id 21886157)1, 4 Suhre K....Gieger C. (2011)
    2. Replication of the five novel loci for uric acid conc entrations and potential mediating mechanisms. (PubMed id 19861489)1, 4 van der Harst P....Navis G. (2010)
    3. A genome-wide perspective of genetic variation in hum an metabolism. (PubMed id 20037589)1, 4 Illig T....Suhre K. (2010)
    4. Meta-analysis of 28,141 individuals identifies common variants within five new loci that influence uric acid concentrations. (PubMed id 19503597)1, 4 Kolz M....Gieger C. (2009)
    5. Common polymorphisms influencing serum uric acid leve ls contribute to susceptibility to gout, but not to coronary artery disease. (PubMed id 19890391)1, 4 Stark K....Hengstenberg C. (2009)
    6. A scan of chromosome 10 identifies a novel locus showing strong association with late-onset Alzheimer disease. (PubMed id 16385451)1, 4 Grupe A....Goate A. (2006)
    7. The SLC16 gene family-from monocarboxylate transporters (MCTs) to aromatic amino acid transporters and beyond. (PubMed id 12739169)1, 2 Halestrap A.P. and Meredith D. (2004)
    8. Complete sequencing and characterization of 21,243 full-length human cDNAs. (PubMed id 14702039)1, 2 Ota T.... Sugano S. (2004)
    9. Genome-wide association analyses identify 18 new loci associated with serum urate concentrations. (PubMed id 23263486)1 Kottgen A....Gieger C. (2013)
    10. A proteome-wide, quantitative survey of in vivo ubiqui tylation sites reveals widespread regulatory roles. (PubMed id 21890473)1 Wagner S.A....Choudhary C. (2011)

    (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: 220963 HGNC: 23520 AceView: SLC16A9 Ensembl:ENSG00000165449 euGenes: HUgn220963
    ECgene: SLC16A9 H-InvDB: SLC16A9

    (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 SLC16A9 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 SLC16A9 gene:
    Search GeneIP for patents involving SLC16A9

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



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