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

WNT6 Gene

protein-coding   GIFtS: 60
GCID: GC02P219724

wingless-type MMTV integration site family, member 6

 Explore 8 diseases affiliated with
WNT6 via our new
 Human Malady Compendium 
Biological research products
for WNT6
    

(According to 1HGNC, 2Entrez Gene,
3UniProtKB/Swiss-Prot, 4UniProtKB/TrEMBL, 5OMIM, 6GeneLoc, 7Ensembl, 8DME, 9miRBase, and/or 10fRNAdb)
About This Section

Aliases
Wingless-Type MMTV Integration Site Family, Member 61 2
Protein Wnt-62

External Ids:    HGNC: 127851   Entrez Gene: 74752   Ensembl: ENSG000001155967   OMIM: 6046635   UniProtKB: Q9Y6F93   

Export aliases for WNT6 gene to outside databases

Previous GC identifers: GC02P217740 GC02P218445 GC02P219688 GC02P219927 GC02P219548 GC02P219432 GC02P211579


(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 WNT6:
The WNT gene family consists of structurally related genes which encode secreted signaling proteins. These proteins
have been implicated in oncogenesis and in several developmental processes, including regulation of cell fate and
patterning during embryogenesis. This gene is a member of the WNT gene family. It is overexpressed in cervical cancer
cell line and strongly coexpressed with another family member, WNT10A, in colorectal cancer cell line. The gene
overexpression may play key roles in carcinogenesis. This gene and the WNT10A gene are clustered in the chromosome
2q35 region. The protein encoded by this gene is 97% identical to the mouse Wnt6 protein at the amino acid level.
(provided by RefSeq, Jul 2008)

UniProtKB/Swiss-Prot: WNT6_HUMAN, Q9Y6F9
Function: Ligand for members of the frizzled family of seven transmembrane receptors. Probable developmental protein.
May be a signaling molecule which affects the development of discrete regions of tissues. Is likely to signal over
only few cell diameters




(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_000002.11  NC_018913.1  NT_005403.17  
Regulatory elements:
   SABiosciences Regulatory transcription factor binding sites in the WNT6 gene promoter:
         MyoD   PPAR-gamma2   
         Other transcription factors

SwitchGear Promoter luciferase reporter plasmidWNT6 promoter sequence
   Search SABiosciences Chromatin IP Primers for WNT6

Epigenetics:
QIAGEN PyroMark CpG Assay predesigned Pyrosequencing DNA Methylation assays in human, mouse, rat WNT6


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

Entrez Gene cytogenetic band: 2q35   Ensembl cytogenetic band:  2q35   HGNC cytogenetic band: 2q35

WNT6 Gene in genomic location: bands according to Ensembl, locations according to (and/or Entrez Gene and/or Ensembl if different)
WNT6 gene location

GeneLoc information about chromosome 2         GeneLoc Exon Structure

GeneLoc location for GC02P219724:  view genomic region     (about GC identifiers)

Start:
219,724,544 bp from pter      End:
219,738,955 bp from pter
Size:
14,412 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: WNT6_HUMAN, Q9Y6F9 (See protein sequence)
Recommended Name: Protein Wnt-6 precursor  
Size: 365 amino acids; 39721 Da
Subunit: Interacts with PORCN (By similarity)
Subcellular location: Secreted, extracellular space, extracellular matrix
Secondary accessions: Q9H1J6 Q9H238

Explore the universe of human proteins at neXtProt for WNT6: NX_Q9Y6F9

Post-translational modifications:

  • Palmitoylation at Ser-228 is required for efficient binding to frizzled receptors. It is also required for subsequent
  • palmitoylation at Cys-76. Palmitoylation is necessary for proper trafficking to cell surface (By similarity)1
  • View modification sites using PhosphoSitePlus2
  • View neXtProt modification sites for NX_Q9Y6F9

  • WNT6 Protein expression data from MOPED and PaxDb:    About this image 
    Estimated protein expression log10 (pmol).

    REFSEQ proteins: NP_006513.1  
    ENSEMBL proteins: 
     ENSP00000233948  
    Reactome Protein details: Q9Y6F9
    Human Recombinant Protein Products: 
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    Novus Biologicals WNT6 Protein
    Novus Biologicals WNT6 Lysates
    Browse Sino Biological Recombinant Proteins
    Browse ProSpec Recombinant Proteins
    Uscn Proteins for WNT6

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

    GO IDQualified GO termEvidencePubMed IDs
    GO:0005576extracellular region NAS--
    GO:0005578proteinaceous extracellular matrix IEA--
    GO:0005615extracellular space IBA--
    GO:0005886plasma membrane IBA--
    GO:0009986cell surface IEA--


    WNT6 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

    WNT6 for domains           About GeneDecksing

    3 InterPro domains/families:
     IPR009143 Wnt6
     IPR005817 Wnt
     IPR018161 Wnt_CS

    Graphical View of Domain Structure for InterPro Entry Q9Y6F9

    ProtoNet protein and cluster: Q9Y6F9

    1 Blocks protein family: IPB005816 Secreted growth factor Wnt protein

    UniProtKB/Swiss-Prot: WNT6_HUMAN, Q9Y6F9
    Similarity: Belongs to the Wnt family


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

    Function Summary:

         UniProtKB/Swiss-Prot: WNT6_HUMAN, Q9Y6F9
    Function: Ligand for members of the frizzled family of seven transmembrane receptors. Probable developmental protein.
    May be a signaling molecule which affects the development of discrete regions of tissues. Is likely to signal over
    only few cell diameters

         Genatlas biochemistry entry for WNT6:
    wingless-type MMTV integration site 6,Drosophila wingless (wg) segment polarity gene homolog,expressed in
    ectoderm,somites,limb and mammary gland in mice,involved in short-range signaling during embryonic patterning

         Summary:  
    During embryonic development, WNT6 as signaling molecule is secreted from the following cells: Surface Ectoderm Cells in Surface Ectoderm It affects the following cells: Meningeal Progenitor Cells in Anterior Meninges

    miRNA
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    SwitchGear 3'UTR luciferase reporter plasmidWNT6 3' UTR sequence
    Inhib. RNA
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    Gene Ontology (GO): 1 molecular function term (GO ID links to tree view):    About this table

    GO IDQualified GO termEvidencePubMed IDs
    GO:0001664G-protein coupled receptor binding IBA--


    WNT6 for ontologies           About GeneDecksing


    1 GenomeRNAi human phenotype for WNT6:
     Cell cycle / mitosis defect 

    Animal Models:
         Mouse knock-out Wnt6tm1Akis for WNT6
         1 MGI mutant phenotype (inferred from 1 allele(MGI details for Wnt6):
     normal 

    WNT6 for phenotypes           About GeneDecksing


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

    Unified GeneCards pathways - 5/14 super-pathways (see all 14About this table 
    See pathways by source

    Super-pathwaycontained gene-specific pathways
    1Wnt Signaling Pathway
    Wnt Signaling Pathway1.00
    Wnt Signaling Pathway0.33
    Wnt Signaling Pathway and Pluripotency0.55
    Wnt signaling pathway0.30
    DNA damage response (only ATM dependent)0.35
    2Basal cell carcinoma
    Basal cell carcinoma1.00
    Wnt Pathway0.37
    Hedgehog signaling pathway0.41
    Melanogenesis0.32
    3Translation_Non-genomic (rapid) action of Androgen Receptor
    Translation_Non-genomic (rapid) action of Androgen Receptor1.00
    Translation Non-genomic (rapid) action of Androgen Receptor0.99
    4Transcription_Androgen Receptor nuclear signaling
    Transcription_Androgen Receptor nuclear signaling1.00
    Transcription Androgen Receptor nuclear signaling0.99
    5Nanog in Mammalian ESC Pluripotency
    Nanog in Mammalian ESC Pluripotency1.00
    GSK3 Signaling0.61

    Pathway sources
    See GeneCards unified pathways
    Show all pathways

    2 EMD Millipore Pathways for WNT6
        Transcription Androgen Receptor nuclear signaling
    Translation Non-genomic (rapid) action of Androgen Receptor

    1 R&D Systems Pathway for WNT6
        Wnt Signaling Pathway

    5/7 Downloadable PowerPoint Slides of QIAGEN Pathway Central Maps for WNT6 (see all 7)
        GSK3 Signaling
    Presenilin-Mediated Signaling
    Colorectal Cancer Metastasis
    Human Embryonic Stem Cell Pluripotency
    Nanog in Mammalian ESC Pluripotency

    1 Tocris Bioscience Pathway for WNT6
        Wnt Pathway

    2 GeneGo (Thomson Reuters) Pathways for WNT6
        Transcription Androgen Receptor nuclear signaling
    Translation Non-genomic (rapid) action of Androgen Receptor

    3 BioSystems Pathways for WNT6 
        Wnt Signaling Pathway and Pluripotency
    DNA damage response (only ATM dependent)
    Wnt Signaling Pathway

    4        Reactome Pathways for WNT6
        Signal Transduction
    Signaling by GPCR
    GPCR ligand binding
    Class B/2 (Secretin family receptors)


    5         Kegg Pathways  (Kegg details for WNT6):
        Wnt signaling pathway
    Hedgehog signaling pathway
    Melanogenesis
    Pathways in cancer
    Basal cell carcinoma


    WNT6 for pathways           About GeneDecksing

    Interactions:

        SABiosciences Gene Network CentralTM Interacting Genes and Proteins Network for WNT6

    STRING Interaction Network Preview (showing 5 interactants - click image to see 17)

    5/17 Interacting proteins for WNT6 (Q9Y6F93 ENSP000002339484) via UniProtKB, MINT, STRING, and/or I2D (see all 17)
    InteractantInteraction Details
    GeneCardExternal ID(s)
    PORCNQ9H2373, ENSP000003223044I2D: score=4 STRING: ENSP00000322304
    CER1ENSP000003702974STRING: ENSP00000370297
    FZD1ENSP000002879344STRING: ENSP00000287934
    FZD10ENSP000002290304STRING: ENSP00000229030
    FZD2ENSP000003239014STRING: ENSP00000323901
    About this table

    Gene Ontology (GO): 5/17 biological process terms (GO ID links to tree view) (see all 17):    About this table

    GO IDQualified GO termEvidencePubMed IDs
    GO:0001658branching involved in ureteric bud morphogenesis IEA--
    GO:0007267cell-cell signaling NAS--
    GO:0009798axis specification IBA--
    GO:0009952anterior/posterior pattern specification IBA--
    GO:0010628positive regulation of gene expression IMP--


    WNT6 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
    EMD Millipore small molecules for WNT6:
    Small Molecule - inhibitor
    Browse drugs & compounds from Enzo Life Sciences

    Browse Tocris compounds for WNT6
    Search CenterWatch for drugs/clinical trials and news about WNT6 

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

    REFSEQ mRNAs for WNT6 gene: 
    NM_006522.3  

    Unigene Cluster for WNT6:

    Wingless-type MMTV integration site family, member 6
    Hs.29764  [show with all ESTs]
    Unigene Representative Sequence: AY009401
    2 Ensembl transcripts including schematic representations, and UCSC links where relevant:
    ENST00000233948(uc002vjc.1) ENST00000486233

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    hsa-miR-525-5p hsa-miR-520a-5p
    SwitchGear 3'UTR luciferase reporter plasmidWNT6 3' UTR sequence
    Inhib. RNA
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      QIAGEN QuantiTect SYBR Green Assays in human, mouse, rat WNT6
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    Additional cDNA sequence: 

    AB059570.1 AK075522.1 AY009401.1 BC004329.1 BT007456.1 

    3 DOTS entries:

    DT.112442  DT.91749172  DT.92013055 

    24/28 AceView cDNA sequences (see all 28):

    BU727755 BM763339 BM720290 AK075522 BC004329 BM849242 AI218134 BF568080 
    R78502 AB059570 BM687468 BE392594 NM_006522 BT007456 AY009401 BF568920 
    BE410061 BF058854 CD673352 BE744521 BE382983 AA745754 BF057511 AA807187 

    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™, 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

    WNT6 expression in normal human tissues (normalized intensities)
    See probesets specificity/sensitivity at GeneAnnot
    About this imageBioGPS
    CGAP TAG: GGCACCAACG

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

    About this image

    WNT6 expression in embryonic tissues and stem cells
    Expression by the Database of Embryonic development, Stem cell research, and Regenerative medicine    About this table
    3 LifeMap In Vivo Development Anatomical Compartments/Cells 
    Tissue Anatomical Compartment CellCategory (developmental path)
    HypoblastHypoblastHypoblast CellsExtraembryonic Tissues
    KidneyUreteric BudUreteric Bud Tip CellsKidney
    KidneyUreteric BudKidney
    Expression: Positive    Negative     Selective marker
    Experimental details: Curated     Microarrays     In-situ hybridization

    See WNT6 Protein Expression from SPIRE MOPED and PaxDB
    Genevestigator expression for WNT6

    SOURCE GeneReport for Unigene cluster: Hs.29764
        SABiosciences Expression via Pathway-Focused PCR Arrays including WNT6: 
              Notch Signaling Targets in human mouse rat
              Hedgehog Signaling Pathway in human mouse rat
              WNT Signaling Pathway in human mouse rat
              Signal Transduction PathwayFinder in human mouse rat

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    In Situ
    Assay Products:
     

     
    Search Advanced Cell Diagnostics for RNAscope RNA in situ hybridization assays for WNT6

    (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 WNT6 gene from 4/18 species (see all 18)    About this table
    Organism Taxonomic
    classification
    Gene Description Human
    Similarity
    Orthology
    Type
    Details
    chicken
    (Gallus gallus)
    Aves WNT61 wingless-type MMTV integration site family, member more 75.52(n)
    75.62(a)
      395235  NM_001007594.2  NP_001007595.1 
    lizard
    (Anolis carolinensis)
    Reptilia WNT66
    --
    77(a)
    1 ↔ 1
    AAWZ02035345(29263-45616)
    zebrafish
    (Danio rerio)
    Actinopterygii LOC5618311 novel protein similar to vertebrate wingless-type MMTV more 67.76(n)
    73.21(a)
      561831  XM_003199189.1  XP_003199237.1 
    fruit fly
    (Drosophila melanogaster)
    Insecta Wnt61 , 3 frizzled-2 receptor signaling pathway signal
    transducer3
    CG4969-PB1
    49(a)3
    54.31(n)1
    45.22(a)1
      27F33
    340101  NM_135264.31  NP_609108.31 


    ENSEMBL Gene Tree for WNT6 (if available)
    TreeFam Gene Tree for WNT6 (if available) 

    (Paralogs according to 1HomoloGene,
    2Ensembl, and 3SIMAP, Pseudogenes according to 4Pseudogene.org Build 68)
    About This Section
    Paralogs for WNT6 gene
    WNT5B2  WNT162  WNT5A2  WNT112  WNT22  WNT2B2  WNT3A2  WNT12  
    WNT10B2  WNT42  WNT7A2  WNT7B2  WNT10A2  WNT32  
    18 SIMAP similar genes for WNT6 using alignment to 2 protein entries:     WNT6_HUMAN (see all proteins):
    WNT4    WNT2B    WNT2    WNT7B    WNT5A    WNT3
    WNT9B    WNT5B    WNT1    WNT11    WNT7A    WNT3A
    WNT10B    WNT8B    WNT8A    WNT10A    WNT9A    WNT16

    WNT6 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

    10/194 NCBI SNPs in WNT6 are shown (see all 194    About this table
    Genomic DataTranscription Related DataAllele Frequencies
    SNP IDValidClinical
    significance
    Chr 2 posSequence#AA
    Chg
    TypeMore#Allele
    freq
    PopTotal
    sample
    More
    ----------
    rs6908771,2
    C,F,A,H,--219722664(+) ACCTGC/TAGCCT 1 -- us2k128Minor allele frequency- T:0.21NA EA NS WA CSA 2379
    rs1902304971,2
    --219722736(+) AAACTC/GGGTAT 1 -- us2k10--------
    rs1488298241,2
    --219722802(+) TGGCAC/TTGCCC 1 -- us2k10--------
    rs1818825351,2
    --219722809(+) GCCCCA/GTAGAA 1 -- us2k10--------
    rs1469223471,2
    --219723107(+) TCATTC/TCTTCC 1 -- us2k10--------
    rs779781591,2
    F,--219723268(+) GAAGCG/AACCTC 1 -- us2k11Minor allele frequency- A:0.02WA 118
    rs1151202551,2
    C,F,--219723379(+) AGGACA/GGCTTT 1 -- us2k11Minor allele frequency- G:0.14WA 118
    rs98080111,2
    C,F,H,--219723431(+) TCCCAC/TACCAC 1 -- us2k1 tfbs36Minor allele frequency- T:0.05NS NA WA 906
    rs1853202261,2
    --219723447(+) CCTTGA/GCACCC 1 -- us2k10--------
    rs1378919221,2
    --219723698(+) CTCTTA/GGACAC 1 -- us2k10--------

    HapMap Linkage Disequilibrium report for WNT6 (219724544 - 219738955 bp)
    Structural Variations (Copy Number Variations, Insertions/Deletions, Inversions)
          Database of Genomic Variants (DGV) variations for WNT6: --

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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

    WNT6 for disorders           About GeneDecksing

    OMIM gene information: 604663    OMIM disorders: --

    8 diseases for WNT6:    About MalaCards
    cervical cancer    colorectal cancer    cervicitis    ectodermal dysplasia
    basal cell carcinoma    hermaphroditism    carcinoma    neuronitis

    Human Genome Epidemiology (HuGE) Navigator: WNT6 (2 documents)

    Export disorders for WNT6 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 WNT6 gene, integrated from 9 sources (see all 22):
    (articles sorted by number of sources associating them with WNT6)
        Utopia: connect your pdf to the dynamic
    world of online information

    1. WNT10A and WNT6, clustered in human chromosome 2q35 region with head- to-tail manner, are strongly co-expressed in SW480 cells. (PubMed id 11350055)1, 2, 3, 9 Kirikoshi H.... Katoh M. (2001)
    2. Partial cloning and assignment of WNT6 to human chromosome band 2q35 by in situ hybridization. (PubMed id 10343101)1, 2, 3 Rankin J.... Lindsay S. (1999)
    3. 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)
    4. Polymorphisms in WNT6 and WNT10A and colorectal adeno ma risk. (PubMed id 21547848)1 Galbraith R.L....Ulrich C.M. (2011)
    5. Maternal genes and facial clefts in offspring: a comp rehensive search for genetic associations in two population-based cleft studies from Scandinavia. (PubMed id 20634891)1 Jugessur A....Murray J.C. (2010)
    6. Effect of Wnt6 on human dental papilla cells in vitro . (PubMed id 20113781)1 Wang C....Ye L. (2010)
    7. Mutation in WNT10A is associated with an autosomal recessive ectodermal dysplasia: the odonto-onycho-dermal dysplasia. (PubMed id 17847007)1 Adaimy L.... Megarbane A. (2007)
    8. Analysis of candidate genes on chromosome 2 in oral cleft case-parent trios from three populations. (PubMed id 16953426)1 Beaty T.H....Scott A.F. (2006)
    9. Expression patterns of Wnt genes during development of an anterior part of the chicken eye. (PubMed id 16258938)1 Fokina V.M. and Frolova E.I. (2006)
    10. Signal sequence and keyword trap in silico for selection of full- length human cDNAs encoding secretion or membrane proteins from oligo- capped cDNA libraries. (PubMed id 16303743)1 Otsuki T....Isogai T. (2005)

    (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: 7475 HGNC: 12785 AceView: WNT6 Ensembl:ENSG00000115596 euGenes: HUgn7475
    ECgene: WNT6 Kegg: 7475 H-InvDB: WNT6

    (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 WNT6 Pharmacogenomics, SNPs, Pathways
    ATLAS Chromosomes in Cancer entry for WNT6 Genetics and Cytogenetics in Oncology and Haematology

    (Patent information from GeneIP,
    Licensable technologies from WIS Yeda, Salk, Tufts,
    IP news from LifeMap Sciences, Inc.)
    About This Section
    Patent Information for WNT6 gene:
    Search GeneIP for patents involving WNT6

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



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