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SNX11 Gene

protein-coding   GIFtS: 47
GCID: GC17P046184

Sorting Nexin 11

  Search for SNX11
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 111 2
Sorting Nexin-112

External Ids:    HGNC: 149751   Entrez Gene: 299162   Ensembl: ENSG000000029197   OMIM: 6149065   UniProtKB: Q9Y5W93   

Export aliases for SNX11 gene to outside databases

Previous GC identifers: GC17P045890 GC17P048665 GC17P046526 GC17P046659 GC17P043539 GC17P041555


(According to Entrez Gene, GeneCards, Tocris Bioscience, Wikipedia's Gene Wiki, PharmGKB,
UniProtKB/Swiss-Prot, and/or UniProtKB/TrEMBL)
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Entrez Gene summary for SNX11 Gene:
This gene encodes a member of the sorting nexin family. Members of this family contain a phox (PX) domain, which
is a phosphoinositide binding domain, and are involved in intracellular trafficking. This protein does not
contain a coiled coil region, like some family members. This gene encodes a protein of unknown function. This
gene results in two transcript variants differing in the 5' UTR, but encoding the same protein. (provided by
RefSeq, Jul 2008)

GeneCards Summary for SNX11 Gene:
SNX11 (sorting nexin 11) is a protein-coding gene. GO annotations related to this gene include phosphatidylinositol phosphate binding. An important paralog of this gene is SNX10.

UniProtKB/Swiss-Prot: SNX11_HUMAN, Q9Y5W9
Function: Phosphoinositide-binding protein involved in protein sorting and membrane trafficking in endosomes




(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_000017.11  NT_010783.16  NC_018928.2  
Regulatory elements:
   Regulatory transcription factor binding sites in the SNX11 gene promoter:
         CREB   Tal-1   deltaCREB   Pax-4a   E47   
         Other transcription factors

SwitchGear Promoter luciferase reporter plasmidSNX11 promoter sequence
   Search Chromatin IP Primers for SNX11

Epigenetics:
DNA Methylation CpG Assay Predesigned for Pyrosequencing in human, mouse, rat SNX11


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

Entrez Gene cytogenetic band: 17q21.32   Ensembl cytogenetic band:  17q21.32   HGNC cytogenetic band: 17q21.32

SNX11 Gene in genomic location: bands according to Ensembl, locations according to (and/or Entrez Gene and/or Ensembl if different)
SNX11 gene location

GeneLoc information about chromosome 17         GeneLoc Exon Structure

GeneLoc location for GC17P046184:  view genomic region     (about GC identifiers)

Start:
46,180,719 bp from pter      End:
46,200,436 bp from pter
Size:
19,718 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: SNX11_HUMAN, Q9Y5W9 (See protein sequence)
Recommended Name: Sorting nexin-11  
Size: 270 amino acids; 30433 Da
Subunit: Monomer
Sequence caution: Sequence=AAD27834.1; Type=Erroneous initiation; Note=Translation N-terminally extended;
2 PDB 3D structures from and Proteopedia for SNX11:
4IKB (3D)        4IKD (3D)    
Secondary accessions: B3KRL6 D3DTV0 Q53YC0 Q9H885

Explore the universe of human proteins at neXtProt for SNX11: NX_Q9Y5W9

Explore proteomics data for SNX11 at MOPED

Post-translational modifications: 

  • Modification sites at neXtProt
  • Modification sites at PhosphoSitePlus

  • See SNX11 Protein Expression from SPIRE MOPED, PaxDB, and MaxQB

    REFSEQ proteins (2 alternative transcripts): 
    NP_037455.2  NP_689450.1  

    ENSEMBL proteins: 
     ENSP00000464136   ENSP00000462188   ENSP00000396790   ENSP00000377059   ENSP00000464410  
     ENSP00000352175   ENSP00000463250   ENSP00000463948   ENSP00000463726   ENSP00000463076  
     ENSP00000407369  

    SNX11 Human Recombinant Protein Products:

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    Cloud-Clone Corp. CLIAs for SNX11


    (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

    2 InterPro protein domains:
     IPR001683 Phox
     IPR028655 SNX11

    Graphical View of Domain Structure for InterPro Entry Q9Y5W9

    ProtoNet protein and cluster: Q9Y5W9

    1 Blocks protein domain: IPB001683 Phox-like

    UniProtKB/Swiss-Prot: SNX11_HUMAN, Q9Y5W9
    Domain: The PX domain mediates interaction with membranes enriched in phosphatidylinositol 3-phosphate
    (PubMed:23615901)
    Similarity: Belongs to the sorting nexin family
    Similarity: Contains 1 PX (phox homology) domain


    SNX11 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: SNX11_HUMAN, Q9Y5W9
    Function: Phosphoinositide-binding protein involved in protein sorting and membrane trafficking in endosomes

         Gene Ontology (GO): 2 molecular function terms:    About this table

    GO IDQualified GO termEvidencePubMed IDs
    GO:0035091phosphatidylinositol binding ----
    GO:1901981phosphatidylinositol phosphate binding IDA--
         
    SNX11 for ontologies           About GeneDecksing


    Phenotypes:
         1 GenomeRNAi human phenotype for SNX11:
     Decreased viability of wild-ty 

    Animal Models:
       inGenious Targeting Laboratory: Let us create your new Knockout/Knockin mouse model for SNX11
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    miRNA
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    miRTarBase miRNAs that target SNX11:
    hsa-mir-484 (MIRT042365), hsa-mir-151a-5p (MIRT038195), hsa-mir-128-3p (MIRT045867)

    Block miRNA regulation of human, mouse, rat SNX11 using miScript Target Protectors
    Selected qRT-PCR Assays for microRNAs that regulate SNX11 (see all 10):
    hsa-miR-3173-3p hsa-miR-4289 hsa-miR-146a* hsa-miR-1233 hsa-miR-3926 hsa-miR-2355-5p hsa-miR-214 hsa-miR-3622b-3p
    SwitchGear 3'UTR luciferase reporter plasmidSNX11 3' UTR sequence
    Inhib. RNA
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    Sino Biological Human cDNA Clone for SNX11
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    Vector BioLabs ready-to-use adenovirus/AAV for human, mouse, rat SNX11

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    In Situ Assay
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    Advanced Cell Diagnostics RNAscope RNA in situ hybridization assays for SNX11


    (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
    SNX11_HUMAN, Q9Y5W9: Membrane; Peripheral membrane protein; Cytoplasmic side (Potential). Endosome
    Subcellular locations from COMPARTMENTS: 

    CompartmentConfidence
    cytosol3
    nucleus2
    extracellular1

    Gene Ontology (GO): 2 cellular component terms:    About this table

    GO IDQualified GO termEvidencePubMed IDs
    GO:0005768endosome IDA--
    GO:0016020membrane IEA--

    SNX11 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 SNX11
    Interactions:

        Search GeneGlobe Interaction Network for SNX11

    STRING Interaction Network Preview (showing 5 interactants - click image to see 11)

    Selected Interacting proteins for SNX11 (ENSP000003521754) via UniProtKB, MINT, STRING, and/or I2D (see all 11)
    InteractantInteraction Details
    GeneCardExternal ID(s)
    PIN1ENSP000002479704STRING: ENSP00000247970
    EIF1AXENSP000003689274STRING: ENSP00000368927
    EIF1AYENSP000003547224STRING: ENSP00000354722
    VPS35ENSP000002991384STRING: ENSP00000299138
    TSG101ENSP000002519684STRING: ENSP00000251968
    About this table

    Gene Ontology (GO): 4 biological process terms:    About this table

    GO IDQualified GO termEvidencePubMed IDs
    GO:0006886intracellular protein transport IBA--
    GO:0007154cell communication ----
    GO:0015031protein transport ----
    GO:0016050vesicle organization IMP--

    SNX11 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 SNX11



    (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 SNX11 gene (2 alternative transcripts): 
    NM_013323.2  NM_152244.1  

    Unigene Cluster for SNX11:

    Sorting nexin 11
    Hs.15827  [show with all ESTs]
    Unigene Representative Sequence: AK023932
    14 Ensembl transcripts including schematic representations, and UCSC links where relevant:
    ENST00000581298 ENST00000578861 ENST00000580219 ENST00000452859 ENST00000393405(uc010wlg.1 uc002inf.1 uc002ing.1 uc010wlh.1 uc010wli.1 uc010wlj.1 uc002inh.1)
    ENST00000580875 ENST00000581705 ENST00000359238 ENST00000583320 ENST00000582104
    ENST00000584335 ENST00000582481 ENST00000577310 ENST00000439357
    miRNA
    Products:
         
    Block miRNA regulation of human, mouse, rat SNX11 using miScript Target Protectors
    Selected qRT-PCR Assays for microRNAs that regulate SNX11 (see all 10):
    hsa-miR-3173-3p hsa-miR-4289 hsa-miR-146a* hsa-miR-1233 hsa-miR-3926 hsa-miR-2355-5p hsa-miR-214 hsa-miR-3622b-3p
    SwitchGear 3'UTR luciferase reporter plasmidSNX11 3' UTR sequence
    Inhib. RNA
    Products:
         
    OriGene RNAi products in human, mouse, rat for SNX11
    Predesigned siRNA for gene silencing in human, mouse, rat SNX11
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    OriGene ORF clones in mouse, rat for SNX11
    OriGene custom cloning services - gene synthesis, subcloning, mutagenesis, variant library, vector shuttling
    GenScript: all cDNA clones in your preferred vector (see all 2): SNX11 (NM_152244)
    DNA2.0 Custom Codon Optimized Gene Synthesis Service for SNX11
    Vector BioLabs ready-to-use adenovirus/AAV for human, mouse, rat SNX11
    Primer
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    OriGene qPCR primer pairs and template standards for SNX11
    OriGene qSTAR qPCR primer pairs in human, mouse for SNX11
    Pre-validated RT2 qPCR Primer Assay in human, mouse, rat SNX11
      QuantiTect SYBR Green Assays in human, mouse, rat SNX11
      QuantiFast Probe-based Assays in human, mouse, rat SNX11

    Additional mRNA sequence: 

    AF121861.1 AK023932.1 AK091852.1 AK296095.1 AK296569.1 AK298551.1 AK316374.1 BC000768.2 
    BC103721.1 BT006723.1 

    9 DOTS entries:

    DT.91746218  DT.114427  DT.100790793  DT.97770690  DT.95247427  DT.91746215  DT.91746214  DT.40260059 
    DT.92056707 

    Selected AceView cDNA sequences (see all 177):

    AI369845 AI359942 AU156808 BX956358 NM_013323 AV647064 BG231638 BU739766 
    BC000768 BQ433082 AL598906 BU172036 AA552016 BI760338 BU167301 NM_152244 
    BM820627 AI202171 BQ022488 AI734245 CR593364 H67933 BX401094 BQ435064 

    GeneLoc Exon Structure

    Selected Alternative Splicing Database (ASD) splice patterns (SP) for SNX11 (see all 11)    About this scheme

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


    ECgene alternative splicing isoforms for SNX11

    (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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    SNX11 expression in normal human tissues (normalized intensities)
    See probesets specificity/sensitivity at GeneAnnot
    About this imageBioGPS <intensity>2/3
    CGAP TAG: GCATTTAGTT
    SNX11 Expression
    About this image


    SNX11 expression in embryonic tissues and stem cells    About this table
    Data from LifeMap, the Embryonic Development and Stem Cells Database
     
     Neural Tube (Nervous System)
             Metencephalon
    SNX11 Protein expression data from MOPED1, PaxDb2 and MaxQB3    About this image

    SNX11 Protein Expression

    SOURCE GeneReport for Unigene cluster: Hs.15827
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    In Situ
    Assay Products:
     

     
    Advanced Cell Diagnostics RNAscope RNA in situ hybridization assays for SNX11

    (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 and fungi.

    Orthologs for SNX11 gene from Selected species (see all 14)    About this table
    Organism Taxonomic
    classification
    Gene Description Human
    Similarity
    Orthology
    Type
    Details
    mouse
    (Mus musculus)
    Mammalia Snx111 , 5 sorting nexin 111, 5 82.96(n)1
    84.44(a)1
      11 (60.10 cM)5
    744791  NM_001163389.11  NP_001156861.11 
     967675555 
    chicken
    (Gallus gallus)
    Aves SNX111 sorting nexin 11 76.68(n)
    78.69(a)
      429353  XM_004948569.1  XP_004948626.1 
    lizard
    (Anolis carolinensis)
    Reptilia SNX116
    sorting nexin 11
    88(a)
    1 ↔ 1
    6(75001101-75024588)
    tropical clawed frog
    (Xenopus tropicalis)
    Amphibia Str.152242 Transcribed sequence with moderate similarity to protein spQ9Y5W9 (H.sapiens) SNXB_HUMAN Sorting nexin 11 less 73.38(n)    AL869614.2 
    zebrafish
    (Danio rerio)
    Actinopterygii Dr.162732 Transcribed sequence with moderate similarity to protein spQ9Y5W9 (H.sapiens) SNXB_HUMAN Sorting nexin 11 less 77.92(n)    BI473731.1 
    baker's yeast
    (Saccharomyces cerevisiae)
    Saccharomycetes SNX36
    Sorting nexin required to maintain late-Golgi resi...
    26(a)
    1 → many
    XV(1009224-1009712) YOR357C


    ENSEMBL Gene Tree for SNX11 (if available)
    TreeFam Gene Tree for SNX11 (if available)

    (Paralogs according to 1HomoloGene,
    2Ensembl, and 3SIMAP, Pseudogenes according to 4Pseudogene.org Build 68)
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    Paralogs for SNX11 gene
    SNX102  SNX32  SNX122  
    3 SIMAP similar genes for SNX11 using alignment to 9 protein entries:     SNX11_HUMAN (see all proteins):
    SNX10    SNX3    SNX12

    SNX11 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 SNX11 (see all 363)    About this table    
    Genomic DataTranscription Related DataAllele Frequencies
    SNP IDValidClinical
    significance
    Chr 17 posSequence#AA
    Chg
    TypeMore#Allele
    freq
    PopTotal
    sample
    More
    ----------
    rs1911603081,2
    --41552708(+) CTTGAG/TAGTTC 1 -- us2k10--------
    rs1830094691,2
    --41552786(+) GGTGGC/TACACA 1 -- us2k10--------
    rs1507766431,2
    --46183048(+) GGCACA/GGTGGC 2 -- us2k10--------
    rs99105161,2
    C,F--46183160(+) taaaaG/Atacaa 2 -- us2k15Minor allele frequency- A:0.44NA WA CSA 9
    rs344494971,2
    C,F--46183189(+) GGCGCA/GTGCCT 2 -- us2k14Minor allele frequency- G:0.30NA 10
    rs562581991,2
    C,F--46183246(+) AGATCA/GGTGAT 2 -- us2k14Minor allele frequency- G:0.20WA NA 242
    rs2014656291,2
    --46183269(+) TGTGA-/TTTTTT 2 -- us2k10--------
    rs1471546881,2
    --46183285(+) ATTGAA/CTAAAT 2 -- us2k10--------
    rs99107891,2
    C,F,H--46183289(+) aataaA/Ctgcat 2 -- us2k14Minor allele frequency- C:0.00NS EA 386
    rs1866037261,2
    --46183385(+) CCATCG/TCCAAG 2 -- us2k10--------

    HapMap Linkage Disequilibrium report for SNX11 (46180719 - 46200436 bp)

    Structural Variations
         Database of Genomic Variants (DGV) 4 variations for SNX11:    About this table    
    Variant IDTypeSubtypePubMed ID
    esv1007058CNV Deletion20482838
    nsv112217CNV Loss16902084
    nsv908576CNV Gain21882294
    nsv469808CNV Complex16826518

    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: 614906    OMIM disorders: --


    SNX11 for disorders           About GeneDecksing


    Export disorders for SNX11 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 SNX11 gene integrated from 10 sources:
    (articles sorted by number of sources associating them with SNX11)
        Utopia: connect your pdf to the dynamic
    world of online information

    1. Structure of Sorting Nexin 11 (SNX11) reveals a novel extended PX Domain (PXe Domain) critical for the inhibition of Sorting Nexin 10 (SNX10) induced vacuolation. (PubMed id 23615901)1, 2 Xu J.... Liu J. (J. Biol. Chem. 2013)
    2. 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)
    3. Complete sequencing and characterization of 21,243 full-length human cDNAs. (PubMed id 14702039)1, 2 Ota T.... Sugano S. (Nat. Genet. 2004)
    4. A large family of endosome-localized proteins related to sorting nexin 1. (PubMed id 11485546)1, 2 Teasdale R.D.... Gleeson P.A. (Biochem. J. 2001)
    5. Genome-wide association analysis of genetic generalized epilepsies implicates susceptibility loci at 1q43, 2p16.1, 2q22.3 and 17q21.32. (PubMed id 22949513)1  ....Sander T. (Hum. Mol. Genet. 2012)
    6. Systems-wide analysis of ubiquitylation dynamics reveals a key role for PAF15 ubiquitylation in DNA-damage bypass. (PubMed id 23000965)1 Povlsen L.K....Choudhary C. (Nat. Cell Biol. 2012)
    7. Mass spectrometric analysis of lysine ubiquitylation reveals promiscuity at site level. (PubMed id 21139048)1 Danielsen J.M....Nielsen M.L. (amp 2011)
    8. 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)
    9. Sorting out the cellular functions of sorting nexins. (PubMed id 12461558)1 Worby C.A. and Dixon J.E. (Nat. Rev. Mol. Cell Biol. 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: 29916 HGNC: 14975 AceView: SNX11 Ensembl:ENSG00000002919 euGenes: HUgn29916
    ECgene: SNX11 H-InvDB: SNX11

    (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 SNX11 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 SNX11 gene:
    Search GeneIP for patents involving SNX11

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



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