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SNX32 Gene

protein-coding   GIFtS: 49
GCID: GC11P065601

Sorting Nexin 32

(Previous name: sorting nexin 6B)
(Previous symbol: SNX6B)
  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)
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Aliases
Sorting Nexin 321 2
SNX6B1 2 3
Sorting Nexin 6B1 2
Sorting Nexin-6B2 3
Sorting Nexin-322

External Ids:    HGNC: 264231   Entrez Gene: 2541222   Ensembl: ENSG000001728037   UniProtKB: Q86XE03   

Export aliases for SNX32 gene to outside databases

Previous GC identifers: GC11P065357 GC11P061927


(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 SNX32 Gene:
SNX32 (sorting nexin 32) is a protein-coding gene. Diseases associated with SNX32 include inflammatory bowel disease, and breast cancer. GO annotations related to this gene include phosphatidylinositol binding. An important paralog of this gene is SNX6.

UniProtKB/Swiss-Prot: SNX32_HUMAN, Q86XE0
Function: May be involved in several stages of intracellular trafficking (By similarity)




(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_000011.10  NT_167190.2  NC_018922.2  
Regulatory elements:
   Regulatory transcription factor binding sites in the SNX32 gene promoter:
         NF-E2 p45   Gfi-1   RORalpha1   N-Myc   GATA-6   POU2F1   POU2F1a   NF-E2   Pax-4a   ATF6   
         Other transcription factors

SwitchGear Promoter luciferase reporter plasmidSNX32 promoter sequence
   Search Chromatin IP Primers for SNX32

Epigenetics:
DNA Methylation CpG Assay Predesigned for Pyrosequencing in human, mouse, rat SNX32


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

Entrez Gene cytogenetic band: 11q13.1   Ensembl cytogenetic band:  11q13.1   HGNC cytogenetic band: 11q13.1

SNX32 Gene in genomic location: bands according to Ensembl, locations according to (and/or Entrez Gene and/or Ensembl if different)
SNX32 gene location

GeneLoc information about chromosome 11         GeneLoc Exon Structure

GeneLoc location for GC11P065601:  view genomic region     (about GC identifiers)

Start:
65,601,112 bp from pter      End:
65,624,367 bp from pter
Size:
23,256 bases      Orientation:
plus 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, 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., 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: SNX32_HUMAN, Q86XE0 (See protein sequence)
Recommended Name: Sorting nexin-32  
Size: 403 amino acids; 46399 Da
Secondary accessions: Q8IW53 Q96NG4
Alternative splicing: 2 isoforms:  Q86XE0-1   Q86XE0-2   (No experimental confirmation available)

Explore the universe of human proteins at neXtProt for SNX32: NX_Q86XE0

Explore proteomics data for SNX32 at MOPED

Post-translational modifications: 

  • Ubiquitination2 at Lys132

  • See SNX32 Protein Expression from SPIRE MOPED, PaxDB, and MaxQB

    REFSEQ proteins: NP_689973.2  
    ENSEMBL proteins: 
     ENSP00000310620  

    SNX32 Human Recombinant Protein Products:

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    LSBio Antibodies in human, mouse, rat for SNX32

    SNX32 Assay Products:

    Browse Kits and Assays available from EMD Millipore
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    Cloud-Clone Corp. ELISAs for SNX32
    Cloud-Clone Corp. CLIAs for SNX32


    (According to HGNC, IUPHAR, InterPro, ProtoNet, UniProtKB, and/or BLOCKS, Sets of similar genes according to GeneDecks)
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    HGNC Gene Families:
    SNX: Sorting nexins

    4 InterPro protein domains:
     IPR028657 SNX6/SNX32
     IPR015404 Vps5_C
     IPR014637 SNX5/SNX6/SNX32
     IPR001683 Phox

    Graphical View of Domain Structure for InterPro Entry Q86XE0

    ProtoNet protein and cluster: Q86XE0

    1 Blocks protein domain: IPB001683 Phox-like

    UniProtKB/Swiss-Prot: SNX32_HUMAN, Q86XE0
    Similarity: Belongs to the sorting nexin family
    Similarity: Contains 1 PX (phox homology) domain


    SNX32 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,
    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, and Vector BioLabs, Cell Lines from GenScript, ESI BIO, In Situ Hybridization Assays from Advanced Cell Diagnostics, Ontologies according to Gene Ontology Consortium 01 Apr 2014 via Entrez Gene.)
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    Molecular Function:

         UniProtKB/Swiss-Prot Summary: SNX32_HUMAN, Q86XE0
    Function: May be involved in several stages of intracellular trafficking (By similarity)

         Gene Ontology (GO): 1 molecular function term:    About this table

    GO IDQualified GO termEvidencePubMed IDs
    GO:0035091phosphatidylinositol binding IBA--
         
    SNX32 for ontologies           About GeneDecksing


    Animal Models:
       inGenious Targeting Laboratory: Let us create your new Knockout/Knockin mouse model for SNX32
       inGenious Targeting Laboratory: Contact us about creating complex and humanized mouse models for SNX32

       genOway customized KO model: permanent, tissue-specific or time-controlled inactivation for SNX32
       genOway customized Knockin model: humanization, point mutation, expression monitoring, etc. for SNX32

    miRNA
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    miRTarBase miRNAs that target SNX32:
    hsa-mir-335-5p (MIRT018071)

    Block miRNA regulation of human, mouse, rat SNX32 using miScript Target Protectors
    2 qRT-PCR Assays for microRNAs that regulate SNX32:
    hsa-miR-146b-3p hsa-miR-548aa
    SwitchGear 3'UTR luciferase reporter plasmidSNX32 3' UTR sequence
    Inhib. RNA
    Products:
        
    OriGene RNAi products in human, mouse, rat for SNX32
    Predesigned siRNA for gene silencing in human, mouse, rat SNX32

    Gene Editing
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    Clone
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    OriGene custom cloning services - gene synthesis, subcloning, mutagenesis, variant library, vector shuttling
    GenScript: all cDNA clones in your preferred vector: SNX32 (NM_152760)
    Sino Biological Human cDNA Clone for SNX32
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    Vector BioLabs ready-to-use adenovirus/AAV for human, mouse, rat SNX32

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    Advanced Cell Diagnostics RNAscope RNA in situ hybridization assays for SNX32


    (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 COMPARTMENTS: 

    CompartmentConfidence
    cytosol3
    nucleus2

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

    GO IDQualified GO termEvidencePubMed IDs
    GO:0005768endosome IBA--

    SNX32 for ontologies           About GeneDecksing


    (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 SNX32
    Interactions:

        Search GeneGlobe Interaction Network for SNX32

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

    Selected Interacting proteins for SNX32 (Q86XE03 ENSP000003106204) via UniProtKB, MINT, STRING, and/or I2D (see all 6)
    InteractantInteraction Details
    GeneCardExternal ID(s)
    SNX1Q135963I2D: score=1 
    VPS35ENSP000002991384STRING: ENSP00000299138
    VPS26AENSP000002635594STRING: ENSP00000263559
    VPS26BENSP000002811874STRING: ENSP00000281187
    GIT2ENSP000003474644STRING: ENSP00000347464
    About this table

    Gene Ontology (GO): 3 biological process terms:    About this table

    GO IDQualified GO termEvidencePubMed IDs
    GO:0006886intracellular protein transport IBA--
    GO:0007154cell communication ----
    GO:0015031protein transport ----

    SNX32 for ontologies           About GeneDecksing



    (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 SNX32



    (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, Primers from OriGene, and/or QIAGEN )
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    REFSEQ mRNAs for SNX32 gene: 
    NM_152760.2  

    Unigene Cluster for SNX32:

    Sorting nexin 32
    Hs.591950  [show with all ESTs]
    Unigene Representative Sequence: AL833261
    9 Ensembl transcripts including schematic representations, and UCSC links where relevant:
    ENST00000308342(uc001ofr.3) ENST00000533298(uc010rop.1) ENST00000531503(uc009yqt.3)
    ENST00000531795 ENST00000526972 ENST00000534387 ENST00000524729 ENST00000530101
    ENST00000533236
    miRNA
    Products:
         
    Block miRNA regulation of human, mouse, rat SNX32 using miScript Target Protectors
    2 qRT-PCR Assays for microRNAs that regulate SNX32:
    hsa-miR-146b-3p hsa-miR-548aa
    SwitchGear 3'UTR luciferase reporter plasmidSNX32 3' UTR sequence
    Inhib. RNA
    Products:
         
    OriGene RNAi products in human, mouse, rat for SNX32
    Predesigned siRNA for gene silencing in human, mouse, rat SNX32
    Clone
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    GenScript: all cDNA clones in your preferred vector: SNX32 (NM_152760)
    DNA2.0 Custom Codon Optimized Gene Synthesis Service for SNX32
    Vector BioLabs ready-to-use adenovirus/AAV for human, mouse, rat SNX32
    Primer
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    OriGene qSTAR qPCR primer pairs in human, mouse for SNX32
    Pre-validated RT2 qPCR Primer Assay in human, mouse, rat SNX32
      QuantiTect SYBR Green Assays in human, mouse, rat SNX32
      QuantiFast Probe-based Assays in human, mouse, rat SNX32

    Additional mRNA sequence: 

    AK289587.1 AK293827.1 AK296055.1 AK299512.1 AK309435.1 AK309789.1 AK311588.1 AL833261.1 
    BC040981.2 BC045563.1 

    9 DOTS entries:

    DT.100045768  DT.95361135  DT.102839914  DT.120690027  DT.120690192  DT.100882412  DT.40208580  DT.425826 
    DT.91974206 

    Selected AceView cDNA sequences (see all 124):

    BF933256 AW451684 BE464787 BE219367 BI754340 AL833261 BF724391 W67154 
    BM921257 BI668946 BU608020 BI754354 CD638072 BP348242 NM_152760 AA573956 
    BC045563 BM922209 BI063904 AA434171 BX422808 AA134467 AI688472 AA351390 

    GeneLoc Exon Structure

    Selected Alternative Splicing Database (ASD) splice patterns (SP) for SNX32 (see all 7)    About this scheme

    ExUns: 1a · 1b · 1c · 1d · 1e ^ 2 ^ 3a · 3b · 3c · 3d ^ 4 ^ 5a · 5b · 5c ^ 6a · 6b ^ 7 ^ 8 ^ 9 ^ 10 ^ 11 ^ 12 ^ 13 ^ 14
    SP1:                                -                 -     -                       -                                                               
    SP2:                                -                 -     -                       -                                                               
    SP3:                                -                 -     -                                                                                       
    SP4:                                -           -     -     -                                                                                       
    SP5:                          -     -                 -     -                                                                                       


    ECgene alternative splicing isoforms for SNX32

    (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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    SNX32 expression in normal human tissues (normalized intensities)
    See probesets specificity/sensitivity at GeneAnnot
    About this imageBioGPS <intensity>2/3
    CGAP TAG: GGCATCATAA
    SNX32 Expression
    About this image

    SNX32 Protein expression data from MOPED1, PaxDb2 and MaxQB3    About this image

    SNX32 Protein Expression

    SOURCE GeneReport for Unigene cluster: Hs.591950
        Custom PCR Arrays for SNX32
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    In Situ
    Assay Products:
     

     
    Advanced Cell Diagnostics RNAscope RNA in situ hybridization assays for SNX32

    (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 animals.

    Orthologs for SNX32 gene from Selected species (see all 11)    About this table
    Organism Taxonomic
    classification
    Gene Description Human
    Similarity
    Orthology
    Type
    Details
    mouse
    (Mus musculus)
    Mammalia Snx321 , 5 sorting nexin 321, 5 87.06(n)1
    91.29(a)1
      19 (4.34 cM)5
    2258611  NM_001024560.21  NP_001019731.11 
     54952785 
    zebrafish
    (Danio rerio)
    Actinopterygii si:dkey-28n18.96
    si:dkey-28n18.9
    22(a)
    many ↔ many
    6(40353088-40360278) ENSDARG00000097193
    fruit fly
    (Drosophila melanogaster)
    Insecta Snx66
    Snx6
    47(a)
    1 → many
    2L(8218071-8220741)
    worm
    (Caenorhabditis elegans)
    Secernentea snx-66
    Protein SNX-6, isoform a
    40(a)
    1 → many
    V(17968547-17980082) WBGene00013354


    ENSEMBL Gene Tree for SNX32 (if available)
    TreeFam Gene Tree for SNX32 (if available)

    (Paralogs according to 1HomoloGene,
    2Ensembl, and 3SIMAP, Pseudogenes according to 4Pseudogene.org Build 68)
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    Paralogs for SNX32 gene
    SNX62  SNX52  
    2 SIMAP similar genes for SNX32 using alignment to 1 protein entry:     SNX32_HUMAN:
    SNX6    SNX5

    SNX32 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), 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 SNX32 (see all 572)    About this table    
    Genomic DataTranscription Related DataAllele Frequencies
    SNP IDValidClinical
    significance
    Chr 11 posSequence#AA
    Chg
    TypeMore#Allele
    freq
    PopTotal
    sample
    More
    ----------
    rs1809635301,2
    --65599415(+) AAACAA/GATTCA 1 -- us2k10--------
    rs112273201,2
    C,F--65599432(+) ATATCT/CTTCAC 1 -- us2k11Minor allele frequency- C:0.14EA 120
    rs767560501,2
    C,F--65599538(+) CATGAG/ATAAAT 1 -- us2k11Minor allele frequency- A:0.02NA 120
    rs1861528081,2
    --65599636(+) TCCCCA/GCTGGT 1 -- us2k10--------
    rs777791421,2
    C,F--65599656(+) CTCCTC/TACTAG 1 -- us2k13Minor allele frequency- T:0.16WA NA EA 358
    rs759554111,2
    F--65599676(+) TCTCCG/ACACTT 1 -- us2k12Minor allele frequency- A:0.04CSA WA 120
    rs1155007671,2
    F--65599677(+) CTCCGC/TACTTG 1 -- us2k11Minor allele frequency- T:0.03WA 118
    rs71103851,2
    C,H--65599743(+) TCCACT/CGGTTC 1 -- us2k14Minor allele frequency- C:0.00NS EA 404
    rs798793401,2
    C--65599744(+) CCACTA/GGTTCC 1 -- us2k10--------
    rs1474383731,2
    C--65600058(+) TCCAC-/TCAACCTCA
    GCTTCTCTCTGA
    TTGAT
    1 -- us2k10--------

    HapMap Linkage Disequilibrium report for SNX32 (65601112 - 65624367 bp)

    Structural Variations
         Database of Genomic Variants (DGV) 8 variations for SNX32:    About this table    
    Variant IDTypeSubtypePubMed ID
    esv2744634CNV Deletion23290073
    esv2744633CNV Deletion23290073
    esv2662850CNV Deletion23128226
    nsv897764CNV Loss21882294
    nsv897763CNV Loss21882294
    nsv897736CNV Loss21882294
    dgv1185n71CNV Loss21882294
    dgv393e1CNV Complex17122850

    Site Specific Mutation Identification with PCR Assays
    SeqTarget long-range PCR primers for resequencing SNX32
    DNA2.0 Custom Variant and Variant Library Synthesis for SNX32

    (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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    2 diseases for SNX32:    
    About MalaCards
    inflammatory bowel disease    breast cancer


    SNX32 for disorders           About GeneDecksing


    Export disorders for SNX32 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 SNX32 gene integrated from 10 sources:
    (articles sorted by number of sources associating them with SNX32)
        Utopia: connect your pdf to the dynamic
    world of online information

    1. The Phox (PX) domain proteins and membrane traffic. (PubMed id 16782399)1, 3 Seet L.F. and Hong W. (Biochim. Biophys. Acta 2006)
    2. Complete sequencing and characterization of 21,243 full-length human cDNAs. (PubMed id 14702039)1, 2 Ota T.... Sugano S. (Nat. Genet. 2004)
    3. Large-scale genotyping identifies 41 new loci associated with breast cancer risk. (PubMed id 23535729)1 Michailidou K....Easton D.F. (Nat. Genet. 2013)
    4. Pathway Analysis of ChIP-Seq-Based NRF1 Target Genes Suggests a Logical Hypothesis of their Involvement in the Pathogenesis of Neurodegenerative Diseases. (PubMed id 24250222)1 Satoh J....Yamamoto Y. (Gene Regul Syst Bio 2013)
    5. Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease. (PubMed id 23128233)1 Jostins L....Cho J.H. (Nature 2012)
    6. A proteome-wide, quantitative survey of in vivo ubiquitylation sites reveals widespread regulatory roles. (PubMed id 21890473)1 Wagner S.A....Choudhary C. (amp 2011)
    7. hORFeome v3.1: a resource of human open reading frames representing over 10,000 human genes. (PubMed id 17207965)1 Lamesch P.... Vidal M. (Genomics 2007)
    8. The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC). (PubMed id 15489334)2 Gerhard D.S.... Malek J. (Genome Res. 2004)
    9. Circular rapid amplification of cDNA ends for high-throughput extension cloning of partial genes. (PubMed id 15203218)1 Fu G.K....Stuve L.L. (Genomics 2004)
    10. Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences. (PubMed id 12477932)1 Strausberg R.L....Marra M.A. (Proc. Natl. Acad. Sci. U.S.A. 2002)

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

      Query String
    PubMed
    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: 254122 HGNC: 26423 AceView: FLJ30934 Ensembl:ENSG00000172803 euGenes: HUgn254122
    ECgene: SNX32 H-InvDB: SNX32

    (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)
    About This Section

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    NameDescription
    PharmGKB entry for SNX32 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 SNX32 gene:
    Search GeneIP for patents involving SNX32

    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, LSBio, Gene Editing from DNA2.0. Clones from OriGene, GenScript, Sino Biological, DNA2.0, SwitchGear Genomics, Vector BioLabs, Cell lines from GenScript, and ESI BIO, 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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