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

SNX15 Gene

protein-coding   GIFtS: 57
GCID: GC11P064782

Sorting Nexin 15

  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

This gene clusters with an RNA gene
Subcategory (RNA class): lncRNA

Quality score for the ORGUL clustered with this gene is 3

Aliases
Sorting Nexin 151 2
HSAF0014352
Clone Iota Unknown Protein2
Sorting Nexin-152

External Ids:    HGNC: 149781   Entrez Gene: 299072   Ensembl: ENSG000001100257   OMIM: 6059645   UniProtKB: Q9NRS63   
ORGUL members:         
NONCODE14:n410508      

Export aliases for SNX15 gene to outside databases

Previous GC identifers: GC11P067310 GC11P066463 GC11P065031 GC11P064557 GC11P064538 GC11P064552 GC11P061121


(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 SNX15 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. Overexpression of this gene
results in a decrease in the processing of insulin and hepatocyte growth factor receptors to their mature
subunits. This decrease is caused by the mislocalization of furin, the endoprotease responsible for cleavage of
insulin and hepatocyte growth factor receptors. This protein is involved in endosomal trafficking from the plasma
membrane to recycling endosomes or the trans-Golgi network. Alternative splicing results in multiple transcript
variants. Read-through transcription also exists between this gene and the upstream ADP-ribosylation factor-like
2 (ARL2) gene. (provided by RefSeq, Dec 2010)

GeneCards Summary for SNX15 Gene: 
SNX15 (sorting nexin 15) is a protein-coding gene, and is affiliated with the lncRNA class. Diseases associated with SNX15 include hereditary spastic paraplegia, and mitochondrial disorders. GO annotations related to this gene include protein transporter activity and phosphatidylinositol binding. An important paralog of this gene is RPS6KL1.

UniProtKB/Swiss-Prot: SNX15_HUMAN, Q9NRS6
Function: May be involved in several stages of intracellular trafficking. Overexpression of SNX15 disrupts the
normal trafficking of proteins from the plasma membrane to recycling endosomes or the TGN

Gene Wiki entry for SNX15 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_000011.9  NT_167190.1  NC_018922.2  
Regulatory elements:
   SABiosciences Regulatory transcription factor binding sites in the SNX15 gene promoter:
         STAT1   Tal-1   p53   MAZR   Brachyury   SREBP-1c   E47   SREBP-1b   AREB6   SREBP-1a   
         Other transcription factors

SwitchGear Promoter luciferase reporter plasmidSNX15 promoter sequence
   Search SABiosciences Chromatin IP Primers for SNX15

Epigenetics:
QIAGEN PyroMark CpG Assay predesigned Pyrosequencing DNA Methylation assays in human, mouse, rat SNX15


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

Entrez Gene cytogenetic band: 11q12   Ensembl cytogenetic band:  11q13.1   HGNC cytogenetic band: 11q12

SNX15 Gene in genomic location: bands according to Ensembl, locations according to (and/or Entrez Gene and/or Ensembl if different)
SNX15 gene location

GeneLoc information about chromosome 11         GeneLoc Exon Structure

GeneLoc location for GC11P064782:  view genomic region     (about GC identifiers)

Start:
64,781,654 bp from pter      End:
64,808,044 bp from pter
Size:
26,391 bases      Orientation:
plus 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: SNX15_HUMAN, Q9NRS6 (See protein sequence)
Recommended Name: Sorting nexin-15  
Size: 342 amino acids; 38291 Da
Subunit: Homodimer. Interacts with SNX1, SNX2 and SNX4
Subcellular location: Cytoplasm. Membrane; Peripheral membrane protein; Cytoplasmic side. Cytoplasmic vesicle
membrane; Peripheral membrane protein; Cytoplasmic side
Secondary accessions: Q9NRS5
Alternative splicing: 2 isoforms:  Q9NRS6-1   Q9NRS6-2   

Explore the universe of human proteins at neXtProt for SNX15: NX_Q9NRS6

Explore proteomics data for SNX15 at MOPED 

Post-translational modifications:

  • View modification sites using PhosphoSitePlus
  • View neXtProt modification sites for NX_Q9NRS6

  • SNX15 Protein expression data from MOPED1, PaxDb2 and MAXQB3 :    About this image 

    SNX15 Protein Expression
    REFSEQ proteins (2 alternative transcripts): 
    NP_037438.2  NP_680086.2  

    ENSEMBL proteins: 
     ENSP00000366452   ENSP00000434778   ENSP00000437277   ENSP00000431690   ENSP00000316410  
     ENSP00000436023  

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    Cloud-Clone Corp. Proteins for SNX15 

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

    GO IDQualified GO termEvidencePubMed IDs
    GO:0005730nucleolus IDA--
    GO:0005737cytoplasm IDA--
    GO:0005829cytosol NAS11085978
    GO:0016020membrane NAS11085978
    GO:0030659cytoplasmic vesicle membrane IEA--

    SNX15 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: 
    SNX: Sorting nexins

    2 InterPro protein domains:
     IPR007330 MIT
     IPR001683 Phox

    Graphical View of Domain Structure for InterPro Entry Q9NRS6

    ProtoNet protein and cluster: Q9NRS6

    2 Blocks protein domains:
    IPB001683 Phox-like
    IPB007330 MIT


    UniProtKB/Swiss-Prot: SNX15_HUMAN, Q9NRS6
    Domain: The PX domain mediates interaction with membranes enriched in phosphatidylinositol 3-phosphate (By
    similarity)
    Similarity: Belongs to the sorting nexin family
    Similarity: Contains 1 MIT domain
    Similarity: Contains 1 PX (phox homology) domain


    SNX15 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: SNX15_HUMAN, Q9NRS6
    Function: May be involved in several stages of intracellular trafficking. Overexpression of SNX15 disrupts the
    normal trafficking of proteins from the plasma membrane to recycling endosomes or the TGN

         Gene Ontology (GO): 3 molecular function terms (GO ID links to tree view):    About this table

    GO IDQualified GO termEvidencePubMed IDs
    GO:0005515protein binding ----
    GO:0008565protein transporter activity NAS--
    GO:0035091phosphatidylinositol binding IEA--
         
    SNX15 for ontologies           About GeneDecksing


    Animal Models:
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    (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

    SuperPaths for SNX15 About                                                                                                See pathways by source

    SuperPathContained pathways About
    1PDGFR-beta signaling pathway
    PDGFR-beta signaling pathway


    1 BioSystems Pathway for SNX15
        PDGFR-beta signaling pathway



    Interactions:

        Search SABiosciences Gene Network CentralTM Interacting Genes and Proteins Networks for SNX15

    4 Interacting proteins for SNX15 (Q9NRS62, 3) via UniProtKB, MINT, STRING, and/or I2D
    InteractantInteraction Details
    GeneCardExternal ID(s)
    RABAC1Q9UI142, 3MINT-67772 I2D: score=5 
    TMEM66Q96BY92, 3MINT-64352 I2D: score=4 
    REEP6Q96HR93I2D: score=1 
    RTN4Q9NQC33I2D: score=1 
    About this table

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

    GO IDQualified GO termEvidencePubMed IDs
    GO:0006886intracellular protein transport NAS11085978
    GO:0007154cell communication IEA--

    SNX15 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 SNX15

    Search CenterWatch for drugs/clinical trials and news about SNX15

    (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,
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    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 SNX15 gene (2 alternative transcripts): 
    NM_013306.4  NM_147777.3  

    Unigene Cluster for SNX15:

    Sorting nexin 15
    Hs.80132  [show with all ESTs]
    Unigene Representative Sequence: NR_037650
    8 Ensembl transcripts including schematic representations, and UCSC links where relevant:
    ENST00000301886(uc001oci.4 uc001ock.3) ENST00000377244 ENST00000529673
    ENST00000534637 ENST00000524831 ENST00000352068 ENST00000526702 ENST00000525648

    miRNA
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    8/10 QIAGEN miScript miRNA Assays for microRNAs that regulate SNX15 (see all 10):
    hsa-miR-34c-5p hsa-miR-449b hsa-miR-513a-3p hsa-miR-133b hsa-miR-449a hsa-miR-34a hsa-miR-935 hsa-miR-133a
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      QIAGEN QuantiFast Probe-based Assays in human, mouse, rat SNX15

    Additional mRNA sequence: 

    AF001435.1 AF175267.2 AF175268.1 AK315034.1 AK315642.1 BC009897.2 BC012767.2 BC014520.2 
    BT006631.1 NR_037650.1 

    7 DOTS entries:

    DT.113150  DT.100828277  DT.100828278  DT.92425265  DT.100828276  DT.95296513  DT.102825943 

    24/324 AceView cDNA sequences (see all 324):

    AJ346501 BC014520 NM_013306 CB109435 AA325070 BM853836 BE140389 CB117465 
    CR595019 NM_147777 CB156380 T29292 AI631767 AW297877 AW190262 BM695030 
    BE279801 AA333945 BU730115 BQ957603 CR614003 BC002530 CR619183 BQ691172 

    GeneLoc Exon Structure

    5 Alternative Splicing Database (ASD) splice patterns (SP) for SNX15    About this scheme

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


    ECgene alternative splicing isoforms for SNX15

    (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

    SNX15 expression in normal human tissues (normalized intensities)
    See probesets specificity/sensitivity at GeneAnnot
    About this imageBioGPS <intensity>2/3
    CGAP TAG: TCTGTCTGTC
    SNX15 Expression
    About this image


    See SNX15 Protein Expression from SPIRE MOPED and PaxDB
    Genevestigator expression for SNX15

    SOURCE GeneReport for Unigene cluster: Hs.80132

    UniProtKB/Swiss-Prot: SNX15_HUMAN, Q9NRS6
    Tissue specificity: Widely expressed

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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 SNX15 gene from 5/11 species (see all 11)    About this table
    Organism Taxonomic
    classification
    Gene Description Human
    Similarity
    Orthology
    Type
    Details
    mouse
    (Mus musculus)
    Mammalia Snx151 , 5 sorting nexin 151, 5 84.72(n)1
    88.1(a)1
      19 (4.34 cM)5
    690241  NM_026912.11  NP_081188.11 
     61193995 
    lizard
    (Anolis carolinensis)
    Reptilia SNX156
    Uncharacterized protein
    52(a)
    1 ↔ 1
    GL344077.1(58242-69328)
    zebrafish
    (Danio rerio)
    Actinopterygii snx151 sorting nexin 15 53.05(n)
    47.87(a)
      393352  NM_001111237.1  NP_001104707.1 
    fruit fly
    (Drosophila melanogaster)
    Insecta CG71566
    --
    5(a)
    1 → many
    3R(14065142-14067906)
    worm
    (Caenorhabditis elegans)
    Secernentea rskd-16
    Protein RSKD-1, isoform a
    2(a)
    1 → many
    V(12284058-12288617)


    ENSEMBL Gene Tree for SNX15 (if available)
    TreeFam Gene Tree for SNX15 (if available)

    (Paralogs according to 1HomoloGene,
    2Ensembl, and 3SIMAP, Pseudogenes according to 4Pseudogene.org Build 68)
    About This Section
    Paralogs for SNX15 gene
    RPS6KL12  RPS6KC12  
    1 SIMAP similar gene for SNX15 using alignment to 6 protein entries:     SNX15_HUMAN (see all proteins):
    RPS6KC1

    SNX15 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

    10/355 SNPs in SNX15 are shown (see all 355)    About this table     
    Genomic DataTranscription Related DataAllele Frequencies
    SNP IDValidClinical
    significance
    Chr 11 posSequence#AA
    Chg
    TypeMore#Allele
    freq
    PopTotal
    sample
    More
    ----------
    rs1112725491,2
    C--64712744(+) TGTGA-/CCACT 
            
    CCAAC
    2 -- us2k11Minor allele frequency- CCACT:0.00CSA 2
    rs171465891,2
    C,F,H--64712781(+) TATGTC/TAGAGT 2 -- us2k115Minor allele frequency- T:0.12NA NS EA WA CSA 929
    rs1400681001,2
    --64712809(+) TGTAGA/GTGCTG 2 -- us2k10--------
    rs710496801,2
    C,F--64712865(-) ATCTC-/A/ATCT
    C
    /GTCTCA
    AAAAA
    4 -- us2k1 cds12NA 4
    rs108975431,2
    C,A--64712870(+) TGAGAC/TGGAGT 2 -- us2k11Minor allele frequency- T:0.50NA 2
    rs1864034741,2
    C--64713002(+) GCACCC/TGCCAC 2 -- us2k10--------
    rs1118684371,2
    C,F--64713010(+) CACCAC/TGCCCA 2 -- us2k11Minor allele frequency- T:0.50WA 2
    rs3708290251,2
    C--64713042(+) GAGAC-/GGGGGT 2 -- us2k10--------
    rs1884624861,2
    --64713251(+) CACGCA/GTCTGC 2 -- us2k10--------
    rs5023331,2
    C,F,O,H--64713330(-) CCTGAC/TCTCAG 2 -- us2k127Minor allele frequency- N:0.00MN EA NA NS WA CSA 2916

    HapMap Linkage Disequilibrium report for SNX15 (64781654 - 64808044 bp)

    Structural Variations
         Database of Genomic Variants (DGV) 2 variations for SNX15:    About this table     
    Variant IDTypeSubtypePubMed ID
    dgv1174n71CNV Loss21882294
    nsv526181CNV Gain19592680

    SABiosciences Cancer Mutation PCR Assays
    SeqTarget long-range PCR primers for resequencing SNX15
    DNA2.0 Custom Variant and Variant Library Synthesis for SNX15

    (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: 605964    OMIM disorders: --

    5 diseases for SNX15:    About MalaCards
    hereditary spastic paraplegia    mitochondrial disorders    paraplegia    multiple endocrine neoplasia
    spasticity

    1 disease from the University of Copenhagen DISEASES database for SNX15:
    Paraplegia

    SNX15 for disorders           About GeneDecksing


    Export disorders for SNX15 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 SNX15 gene, integrated from 9 sources (see all 22):
    (articles sorted by number of sources associating them with SNX15)
        Utopia: connect your pdf to the dynamic
    world of online information

    1. 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)
    2. Identification and characterization of snx15, a novel sorting nexin involved in protein trafficking. (PubMed id 11085978)1, 2 Phillips S.A.... Haft C.R. (2001)
    3. Overexpression of a novel sorting nexin, SNX15, affects endosome morphology and protein trafficking. (PubMed id 11208079)1, 3 Barr V.A....Haft C.R. (2000)
    4. A clinical, genetic and candidate gene study of Silver syndrome, a complicated form of hereditary spastic paraplegia. (PubMed id 15372247)1, 9 Warner T.T....Crosby A.H. (2004)
    5. A Y2H-seq approach defines the human protein methyltransferase interactome. (PubMed id 23455924)1 Weimann M.... Stelzl U. (2013)
    6. A census of human soluble protein complexes. (PubMed id 22939629)1 Havugimana P.C....Emili A. (2012)
    7. Initial characterization of the human central proteome. (PubMed id 21269460)2 Burkard T.R.... Colinge J. (2011)
    8. Identification of rare DNA variants in mitochondrial disorders with improved array-based sequencing. (PubMed id 20843780)1 Wang W....Scharfe C. (2010)
    9. Quantitative phosphoproteomic analysis of T cell receptor signaling reveals system-wide modulation of protein-protein interactions. (PubMed id 19690332)2 Mayya V.... Han D.K. (2009)
    10. Proteomic analysis of integrin-associated complexes i dentifies RCC2 as a dual regulator of Rac1 and Arf6. (PubMed id 19738201)1 Humphries J.D....Humphries M.J. (2009)

    (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: 29907 HGNC: 14978 AceView: ARL2andSNX15 Ensembl:ENSG00000110025 euGenes: HUgn29907
    ECgene: SNX15 H-InvDB: SNX15

    (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 SNX15 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 SNX15 gene:
    Search GeneIP for patents involving SNX15

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



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    GeneCards Homepage - Last full update: 23 Oct 2013 - Incrementals: 4 Nov 2013 , 7 Nov 2013 , 23 Jan 2014

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