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

FBXW10 Gene

protein-coding   GIFtS: 48
GCID: GC17P018647

F-box and WD repeat domain containing 10

(Previous names: chromosome 17 open reading frame 1A, F-box and WD-40 domain...)
(Previous symbols: C17orf1, C17orf1A)
 Explore 2 diseases affiliated with
FBXW10 via our new
 Human Malady Compendium 
Biological research products
for FBXW10
    

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

Aliases
F-Box And WD Repeat Domain Containing 101 2     Chromosome 17 Open Reading Frame 1A1
Fbw101 2     SM25H22
HREP1 2     F-Box/WD Repeat-Containing Protein 102
SM2SH21 2     Ubiquitin Ligase Specificity Factor2
F-Box And WD-40 Domain Protein 101 2     F-Box And WD-40 Domain-Containing Protein 103
C17orf11     Ubiquitin Ligase-Specificity Factor3
C17orf1A1     

External Ids:    HGNC: 12111   Entrez Gene: 105172   Ensembl: ENSG000001719317   OMIM: 6116795   UniProtKB: Q5XX133   

Export aliases for FBXW10 gene to outside databases

Previous GC identifers: GC17P018589 GC17P018230


(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 FBXW10:
Members of the F-box protein family, such as FBXW10, are characterized by an approximately 40-amino acid F-box motif.
SCF complexes, formed by SKP1 (MIM 601434), cullin (see CUL1; MIM 603134), and F-box proteins, act as
protein-ubiquitin ligases. F-box proteins interact with SKP1 through the F box, and they interact with ubiquitination
targets through other protein interaction domains (Jin et al., 2004 (PubMed 15520277)).(supplied by OMIM, Mar 2008)

UniProtKB/Swiss-Prot: FBW10_HUMAN, Q5XX13
Function: Probable substrate-recognition component of a SCF (SKP1-CUL1-F-box protein)-type E3 ubiquitin ligase complex
which mediates the ubiquitination and subsequent proteasomal degradation of target proteins. Overexpression is leading
to degradation of CBX5 and CBX1

Gene Wiki entry for FBXW10


(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_000017.10  NC_018928.1  NT_010718.16  
Regulatory elements:
   SABiosciences Regulatory transcription factor binding sites in the FBXW10 gene promoter:
         COUP-TF1   COUP-TF   COUP   FOXO1a   MyoD   HNF-4alpha2   HNF-4alpha1   FOXO1   
         Other transcription factors

SwitchGear Promoter luciferase reporter plasmidFBXW10 promoter sequence
   Search SABiosciences Chromatin IP Primers for FBXW10

Epigenetics:
QIAGEN PyroMark CpG Assay predesigned Pyrosequencing DNA Methylation assays in human, mouse, rat FBXW10


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

Entrez Gene cytogenetic band: 17p12   Ensembl cytogenetic band:  17p11.2   HGNC cytogenetic band: 17p11

FBXW10 Gene in genomic location: bands according to Ensembl, locations according to (and/or Entrez Gene and/or Ensembl if different)
FBXW10 gene location

GeneLoc information about chromosome 17         GeneLoc Exon Structure

GeneLoc location for GC17P018647:  view genomic region     (about GC identifiers)

Start:
18,647,326 bp from pter      End:
18,682,662 bp from pter
Size:
35,337 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: FBW10_HUMAN, Q5XX13 (See protein sequence)
Recommended Name: F-box/WD repeat-containing protein 10  
Size: 1052 amino acids; 119846 Da
Secondary accessions: C9JRY8 C9JZD7 Q8TC00 Q9H0F0
Alternative splicing: 4 isoforms:  Q5XX13-1   Q5XX13-2   Q5XX13-3   Q5XX13-4   (No experimental confirmation available)

Explore the universe of human proteins at neXtProt for FBXW10: NX_Q5XX13

Post-translational modifications:

  • View modification sites using PhosphoSitePlus2
  • View neXtProt modification sites for NX_Q5XX13

  • FBXW10 Protein expression data from MOPED and PaxDb:    About this image 
    Estimated protein expression log10 (pmol).

    REFSEQ proteins (2 alternative transcripts): 
    NP_001254514.1  NP_001254515.1  

    ENSEMBL proteins: 
     ENSP00000379025   ENSP00000310382   ENSP00000463552   ENSP00000306937   ENSP00000379026  
    Reactome Protein details: Q5XX13
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    (According to InterPro, ProtoNet, UniProtKB, and/or BLOCKS, Sets of similar genes according to GeneDecks)
    About This Section

    FBXW10 for domains           About GeneDecksing

    5/6 InterPro domains/families (see all 6):
     IPR019775 WD40_repeat_CS
     IPR001810 F-box_dom_cyclin-like
     IPR001680 WD40_repeat
     IPR020472 G-protein_beta_WD-40_rep
     IPR017986 WD40_repeat_dom

    Graphical View of Domain Structure for InterPro Entry Q5XX13

    ProtoNet protein and cluster: Q5XX13

    UniProtKB/Swiss-Prot: FBW10_HUMAN, Q5XX13
    Similarity: Contains 1 F-box domain
    Similarity: Contains 7 WD repeats


    (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: FBW10_HUMAN, Q5XX13
    Function: Probable substrate-recognition component of a SCF (SKP1-CUL1-F-box protein)-type E3 ubiquitin ligase complex
    which mediates the ubiquitination and subsequent proteasomal degradation of target proteins. Overexpression is leading
    to degradation of CBX5 and CBX1
    Induction: By disease-causing laminin A mutants also inducing CBX5 and CBX1 proteasomal degradation

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    4 GenomeRNAi human phenotypes for FBXW10:
     Decreased influenza A H1N1 (A/  Decreased influenza A/WSN/33 r  Increased gamma-H2AX phosphory  Synthetic lethal with Ras 


    (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  About this table 
    See pathways by source

    Super-pathwaycontained gene-specific pathways
    1Chaperonin-mediated protein folding
    Chaperonin-mediated protein folding1.00
    Association of TriC/CCT with target proteins during biosynthesis0.60
    Protein folding0.91
    2Asparagine N-linked glycosylation
    Metabolism of proteins0.15

    Pathway sources
    See GeneCards unified pathways
    Show all pathways


    4        Reactome Pathways for FBXW10
        Association of TriC/CCT with target proteins during biosynthesis
    Chaperonin-mediated protein folding
    Metabolism of proteins
    Protein folding



    FBXW10 for pathways           About GeneDecksing

    Interactions:

        SABiosciences Gene Network CentralTM Interacting Genes and Proteins Network for FBXW10

    (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
    Browse Small Molecules at EMD Millipore
    Browse drugs & compounds from Enzo Life Sciences

    Browse Tocris compounds for FBXW10
    Search CenterWatch for drugs/clinical trials and news about FBXW10 / FBW10 

    (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 FBXW10 gene (3 alternative transcripts): 
    NM_031456.3  NM_001267585.1  NM_001267586.1  

    Unigene Cluster for FBXW10:

    F-box and WD repeat domain containing 10
    Hs.592128  [show with all ESTs]
    Unigene Representative Sequence: NR_051988
    6 Ensembl transcripts including schematic representations, and UCSC links where relevant:
    ENST00000395665 ENST00000308799(uc002gul.3) ENST00000574478 ENST00000301938
    ENST00000573605 ENST00000395667(uc002guj.3 uc002guk.3 uc010cqh.2)


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    Additional cDNA sequence: 

    AK310383.1 AL136822.1 AY729024.1 NR_051988.1 

    7 DOTS entries:

    DT.99958727  DT.100743137  DT.120937583  DT.100689099  DT.40122744  DT.40273190  DT.91647682 

    24 AceView cDNA sequences:

    BI828401 BV183782 BP369886 NM_031456 BQ774415 BC028364 BV183779 BV179399 
    BV172996 BV167161 BV174334 BV167160 BG724426 AL136822 BV167162 AV721196 
    AI809214 BF979266 BI461612 BG721464 AA634374 BF979797 BU568777 BE502292 

    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

    FBXW10 expression in normal human tissues (normalized intensities)
    See probesets specificity/sensitivity at GeneAnnot
    About this imageBioGPS
    CGAP TAG: GATCAGGAAG

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

    About this image
    See FBXW10 Protein Expression from SPIRE MOPED and PaxDB
    Genevestigator expression for FBXW10

    SOURCE GeneReport for Unigene cluster: Hs.592128
        SABiosciences Expression via Pathway-Focused PCR Arrays including FBXW10: 
              Ubiquitination (Ubiquitylation) Pathway in human mouse rat
              Ubiquitin Ligases in human mouse rat

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    In Situ
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    Advanced Cell Diagnostics RNAscope RNA in situ hybridization assays for FBXW10

    (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 chordates.

    Orthologs for FBXW10 gene from 5/12 species (see all 12)    About this table
    Organism Taxonomic
    classification
    Gene Description Human
    Similarity
    Orthology
    Type
    Details
    mouse
    (Mus musculus)
    Mammalia Fbxw105 F-box and WD-40 domain protein 10   --   11 (38.78 cM) 62847069 
    chicken
    (Gallus gallus)
    Aves --
    Uncharacterized protein
    39(a)
    1 → many
    18(2194666-2204960)
    lizard
    (Anolis carolinensis)
    Reptilia --
    --
    39(a)
    1 → many
    2(106145494-106169139)
    tropical clawed frog
    (Xenopus tropicalis)
    Amphibia BX711433.12   -- 74.72(n)    BX711433.1 
    zebrafish
    (Danio rerio)
    Actinopterygii CR752650.16
    --
    30(a)
    1 → many
    12(37125613-37134954)


    ENSEMBL Gene Tree for FBXW10 (if available)
    TreeFam Gene Tree for FBXW10 (if available) 

    (Paralogs according to 1HomoloGene,
    2Ensembl, and 3SIMAP, Pseudogenes according to 4Pseudogene.org Build 68)
    About This Section
    Paralogs for FBXW10 gene
    ENSG000002515372  ENSG000001814642  CDRT12  
    2 SIMAP similar genes for FBXW10 using alignment to 2 protein entries:     FBW10_HUMAN (see all proteins):
    CDRT1    GNB5

    FBXW10 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

    10/616 NCBI SNPs in FBXW10 are shown (see all 616    About this table
    Genomic DataTranscription Related DataAllele Frequencies
    SNP IDValidClinical
    significance
    Chr 17 posSequence#AA
    Chg
    TypeMore#Allele
    freq
    PopTotal
    sample
    More
    ----------
    rs284968161,2
    --18645326(+) CTGGAA/GCTACA 3 -- us2k10--------
    rs283870121,2
    --18645328(+) GGAACC/TACAGG 3 -- us2k10--------
    rs713722861,2
    C,--18645624(+) CGCTGC/TCCTCT 3 -- us2k12Minor allele frequency- T:0.00NA 4
    rs1852360281,2
    --18645763(+) TTTGAA/GGAGAA 3 -- us2k10--------
    rs1896602591,2
    --18646352(+) GTGCTC/TGCCTT 3 -- us2k10--------
    rs1499068001,2
    --18646623(+) ACATGA/GGCATT 3 -- us2k10--------
    rs1401549121,2
    --18646774(+) ATCTTA/CTCCAT 3 -- us2k10--------
    rs620737431,2
    C--18646827(+) GTTGCT/CTGCTC 3 -- us2k12Minor allele frequency- C:0.25NA WA 4
    rs1833542321,2
    --18646832(+) CTGCTC/TGAGAC 3 -- us2k10--------
    rs1490117711,2
    --18646937(+) GCTGCC/TCAATA 3 -- us2k10--------

    HapMap Linkage Disequilibrium report for FBXW10 (18647326 - 18682662 bp)
    Structural Variations (Copy Number Variations, Insertions/Deletions, Inversions)
    Database of Genomic Variants (DGV): 2 variations for FBXW10
         2 CNVs: 4993 30808

    SABiosciences Cancer Mutation PCR Assays
    QIAGEN SeqTarget long-range PCR primers in human, mouse, rat for resequencing FBXW10
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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

    FBXW10 for disorders           About GeneDecksing

    OMIM gene information: 611679    OMIM disorders: --

    2 diseases for FBXW10:    About MalaCards
    hereditary neuropathies    neuropathy


    Export disorders for FBXW10 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 FBXW10 gene, integrated from 9 sources (see all 11):
    (articles sorted by number of sources associating them with FBXW10)
        Utopia: connect your pdf to the dynamic
    world of online information

    1. Lamin A rod domain mutants target heterochromatin protein 1alpha and beta for proteasomal degradation by activation of F-box protein, FBXW10. (PubMed id 20498703)1, 2 Chaturvedi P. and Parnaik V.K. (2010)
    2. Systematic analysis and nomenclature of mammalian F-box proteins. (PubMed id 15520277)1, 2 Jin J....Harper J.W. (2004)
    3. Towards a catalog of human genes and proteins: sequencing and analysis of 500 novel complete protein coding human cDNAs. (PubMed id 11230166)1, 2 Wiemann S.... Poustka A. (2001)
    4. Dynamics of cullin-RING ubiquitin ligase network revea led by systematic quantitative proteomics. (PubMed id 21145461)1 Bennett E.J....Harper J.W. (2010)
    5. Diversification of transcriptional modulation: large-scale identification and characterization of putative alternative promoters of human genes. (PubMed id 16344560)1 Kimura K.... Sugano S. (2006)
    6. DNA sequence of human chromosome 17 and analysis of rearrangement in the human lineage. (PubMed id 16625196)2 Zody M.C.... Nusbaum C. (2006)
    7. 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. (2004)
    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. (2002)
    9. Genomic structure and physical mapping of C17orf1: a gene associated with the proximal element of the CMT1A-REP binary repeat. (PubMed id 9787083)3 Kennerson M.L.... Nicholson G.A. (1998)
    10. Single test for two hereditary neuropathies, CMT1A an d HNPP. (PubMed id 7586531)3 Kennerson M.L....Nicholson G.A. (1995)

    (in PubMed, OMIM, and NCBI Bookshelf)
    About This Section
     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)
    About This Section
    Entrez Gene: 10517 HGNC: 1211 AceView: FBXW10 Ensembl:ENSG00000171931 euGenes: HUgn10517
    ECgene: FBXW10 H-InvDB: FBXW10

    (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 FBXW10 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 FBXW10 gene:
    Search GeneIP for patents involving FBXW10

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



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    In Situ Hybridization Assays from
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     FBXW10 Proteins, Antibodies, CLIAs, and ELISAs
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    GeneCards Homepage - Last full update: 18 Mar 2013 - Incrementals: 21 Mar 2013 , 15 Apr 2013 , 26 Apr 2013

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    VWF
    (GIFTS: 73)
    von Willebrand factor
    GIFtS Group
    The GeneCards human gene database gene index: 1 3 5 6 A B C D E F G H I J K L M N O P Q R S T U V W X Y Z 


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