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

ZNF17 Gene

protein-coding   GIFtS: 52
GCID: GC19P057922

zinc finger protein 17

(Previous names: zinc finger protein 17 (HPF3, KOX 10) )
 Explore 5 diseases affiliated with
ZNF17 via our new
 Human Malady Compendium 
Biological research products
for ZNF17
    

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

Aliases
Zinc Finger Protein 171 2     Zinc Finger Protein HPF32 3
KOX101 2 3     Zinc Finger Protein KOX102 3
HPF31 2     FLJ408641
Zinc Finger Protein 17 (HPF3, KOX 10)1 2     FLJ460581
KIAA19471 3     FLJ466151

External Ids:    HGNC: 129581   Entrez Gene: 75652   Ensembl: ENSG000001862727   UniProtKB: P170213   

Export aliases for ZNF17 gene to outside databases

Previous GC identifers: GC19P058829 GC19P058376 GC19P062539 GC19P062615 GC19P062616 GC19P062617 GC19P054235


(According to Entrez Gene, Tocris Bioscience, Wikipedia's Gene Wiki, PharmGKB,
UniProtKB/Swiss-Prot, and/or UniProtKB/TrEMBL)
About This Section

UniProtKB/Swiss-Prot: ZNF17_HUMAN, P17021
Function: May be involved in transcriptional regulation




(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_000019.9  NC_018930.1  NT_011109.16  
Regulatory elements:
   SABiosciences Regulatory transcription factor binding sites in the ZNF17 gene promoter:
         HTF   XBP-1   
         Other transcription factors

SwitchGear Promoter luciferase reporter plasmidZNF17 promoter sequence
   Search SABiosciences Chromatin IP Primers for ZNF17

Epigenetics:
QIAGEN PyroMark CpG Assay predesigned Pyrosequencing DNA Methylation assays in human, mouse, rat ZNF17


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

Entrez Gene cytogenetic band: 19q13.4   Ensembl cytogenetic band:  19q13.43   HGNC cytogenetic band: 19q13.43

ZNF17 Gene in genomic location: bands according to Ensembl, locations according to (and/or Entrez Gene and/or Ensembl if different)
ZNF17 gene location

GeneLoc information about chromosome 19         GeneLoc Exon Structure

GeneLoc location for GC19P057922:  view genomic region     (about GC identifiers)

Start:
57,922,529 bp from pter      End:
57,933,307 bp from pter
Size:
10,779 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: ZNF17_HUMAN, P17021 (See protein sequence)
Recommended Name: Zinc finger protein 17  
Size: 662 amino acids; 77204 Da
Subcellular location: Nucleus (Potential)
Sequence caution: Sequence=BAC04956.1; Type=Erroneous initiation; Sequence=BAC05252.1; Type=Erroneous termination;
Positions=461; Note=Translated as Gln;
Secondary accessions: B3KXU2 B3KY20 Q8N7M1 Q8N893 Q8TF54
Alternative splicing: 3 isoforms:  P17021-1   P17021-2   P17021-3   

Explore the universe of human proteins at neXtProt for ZNF17: NX_P17021

Post-translational modifications:

  • View modification sites using PhosphoSitePlus2
  • View neXtProt modification sites for NX_P17021

  • ZNF17 Protein expression data from MOPED and PaxDb:    About this image 
    Estimated protein expression log10 (pmol).

    REFSEQ proteins: NP_008890.2  
    ENSEMBL proteins: 
     ENSP00000302455  
    Reactome Protein details: P17021
    Human Recombinant Protein Products: 
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    Uscn Proteins for ZNF17

    Gene Ontology (GO): 1 cellular component term (GO ID links to tree view):    About this table

    GO IDQualified GO termEvidencePubMed IDs
    GO:0005634nucleus IEA--


    ZNF17 for ontologies           About GeneDecksing



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    Uscn ELISAs and CLIAs for ZNF17


    (According to InterPro, ProtoNet, UniProtKB, and/or BLOCKS, Sets of similar genes according to GeneDecks)
    About This Section

    ZNF17 for domains           About GeneDecksing

    4 InterPro domains/families:
     IPR015880 Znf_C2H2-like
     IPR001909 Krueppel-associated_box
     IPR013087 Znf_C2H2/integrase_DNA-bd
     IPR007087 Znf_C2H2

    Graphical View of Domain Structure for InterPro Entry P17021

    ProtoNet protein and cluster: P17021

    1 Blocks protein family: IPB007086 C2H2-type zinc finger signature

    UniProtKB/Swiss-Prot: ZNF17_HUMAN, P17021
    Similarity: Belongs to the krueppel C2H2-type zinc-finger protein family
    Similarity: Contains 17 C2H2-type zinc fingers
    Similarity: Contains 1 KRAB domain


    (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: ZNF17_HUMAN, P17021
    Function: May be involved in transcriptional regulation

         Genatlas biochemistry entry for ZNF17:
    zinc finger protein 17 (KOX10) (C2H2 type,Kruppel-like)

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

    GO IDQualified GO termEvidencePubMed IDs
    GO:0003677DNA binding IEA--
    GO:0008270zinc ion binding IEA--


    ZNF17 for ontologies           About GeneDecksing


    1 GenomeRNAi human phenotype for ZNF17:
     Cell cycle / mitosis defect 


    (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
    1Generic Transcription Pathway
    Generic Transcription Pathway1.00
    Gene Expression0.46

    Pathway sources
    See GeneCards unified pathways
    Show all pathways


    2        Reactome Pathways for ZNF17
        Generic Transcription Pathway
    Gene Expression



    ZNF17 for pathways           About GeneDecksing

    Interactions:

        Search SABiosciences Gene Network CentralTM Interacting Genes and Proteins Networks for ZNF17

    STRING Interaction Network Preview (showing 1 interactants - click image to see more details)

    1 Interacting protein for ZNF17 (P170213 ENSP000003024554) via UniProtKB, MINT, STRING, and/or I2D
    InteractantInteraction Details
    GeneCardExternal ID(s)
    NDEL1Q9GZM83, ENSP000003339824I2D: score=2 STRING: ENSP00000333982
    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:0006351transcription, DNA-dependent IEA--
    GO:0006355regulation of transcription, DNA-dependent IEA--


    ZNF17 for ontologies           About GeneDecksing



    (Chemical Compounds according to UniProtKB, Enzo Life Sciences, EMD Millipore, Tocris Bioscience HMDB, BitterDB, and/or Novoseek, and Drugs according to DrugBank, Enzo Life Sciences, and/or PharmGKB, with drugs/clinical trials/news search links to CenterWatch)
    About This Section

    ZNF17 for compounds           About GeneDecksing

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

    Browse Tocris compounds for ZNF17
    2 Novoseek chemical compound relationships for ZNF17 gene    About this table
    Compound   -log (P-Val)   Hits   PubMed IDs for Articles with Shared Sentences (# sentences)
    zanamivir 82.7 1 11070006 (1)
    sialic acid 75.8 9 10603317 (2), 8965678 (2), 11711635 (1), 12477836 (1) (see all 6)

    Search CenterWatch for drugs/clinical trials and news about ZNF17 

    (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 ZNF17 gene: 
    NM_006959.2  

    Unigene Cluster for ZNF17:

    Zinc finger protein 17
    Hs.729403  [show with all ESTs]
    Unigene Representative Sequence: AK128471
    1 Ensembl transcript including schematic representation, and UCSC links where relevant:
    ENST00000307658(uc021vck.1 uc002qoo.1 uc002qop.1)

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    Inhib. RNA
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    Additional cDNA sequence: 

    AK097123.1 AK098183.1 AK127948.1 AK128471.1 X52341.1 

    6 DOTS entries:

    DT.101973760  DT.40264556  DT.100020506  DT.100020504  DT.121454074  DT.121454139 

    24/25 AceView cDNA sequences (see all 25):

    X52341 AA454141 AK098183 BU569994 AA604653 AK128471 BX487316 AA418246 
    AK097123 AK127948 AB075827 BQ575507 BP871984 BU681756 BG943376 BQ937753 
    BF064020 NM_006959 BG116989 BM127451 BU664322 D81878 AA418360 CK906093 

    GeneLoc Exon Structure

    4 Alternative Splicing Database (ASD) splice patterns (SP) for ZNF17    About this scheme

    ExUns: 1a · 1b · 1c ^ 2 ^ 3 ^ 4a · 4b · 4c · 4d
    SP1:                                                      
    SP2:                    -                                 
    SP3:                          -                           
    SP4:                    -     -                           


    ECgene alternative splicing isoforms for ZNF17

    (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

    ZNF17 expression in normal human tissues (normalized intensities)
    See probesets specificity/sensitivity at GeneAnnot
    About this imageBioGPS
    CGAP TAG: TGTTGCTTAA

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

    About this image
    See ZNF17 Protein Expression from SPIRE MOPED and PaxDB
    Genevestigator expression for ZNF17

    SOURCE GeneReport for Unigene cluster: Hs.729403
        SABiosciences Custom PCR Arrays for ZNF17
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    In Situ
    Assay Products:
     

     
    Advanced Cell Diagnostics RNAscope RNA in situ hybridization assays for ZNF17

    (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
      --

    ENSEMBL Gene Tree for ZNF17 (if available)
    TreeFam Gene Tree for ZNF17 (if available) 

    (Paralogs according to 1HomoloGene,
    2Ensembl, and 3SIMAP, Pseudogenes according to 4Pseudogene.org Build 68)
    About This Section
    Paralogs for ZNF17 gene
    ZNF5492  ZNF2112  ZNF4172  ZNF7922  ZNF7492  ZNF5512  ZNF7762  ZNF5472  
    ZNF4162  ZNF5482  ZNF3042  ZNF587B2  ZNF7732  ZNF1322  ZIK12  ZNF6712  
    ZNF1342  ZNF4182  ZNF2562  ZNF1542  ZNF5522  ZNF7722  ZNF5302  ZNF4192  
    18/485 SIMAP similar genes for ZNF17 using alignment to 3 protein entries:     ZNF17_HUMAN (see all proteins) (see all similar genes):
    FLJ00301    ZNF78L1    ZSCAN16    DKFZp686N14223    HZF36    kr-znf3
    ZNF81    ZNF345    ZNF502    ZNF    ZNF669    DKFZp313M0722
    DKFZp666C237    ZNF146    ZNF157    ZNF323    ZNF391    ZNF818P

    ZNF17 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

    10/211 NCBI SNPs in ZNF17 are shown (see all 211    About this table
    Genomic DataTranscription Related DataAllele Frequencies
    SNP IDValidClinical
    significance
    Chr 19 posSequence#AA
    Chg
    TypeMore#Allele
    freq
    PopTotal
    sample
    More
    ----------
    rs1896090331,2
    --57920539(+) ACTCAA/GGAGGC 1 -- us2k10--------
    rs1810952861,2
    --57920580(+) GCAGAG/TGTTGC 1 -- us2k10--------
    rs1869614021,2
    --57920666(+) AGTTTA/GTTTAG 1 -- us2k10--------
    rs1393213461,2
    --57920676(+) TTCTG-/TTTGGT 1 -- us2k10--------
    rs72461311,2
    C,F,A,H,--57920771(+) GAGACG/AGGGAT 1 -- us2k127Minor allele frequency- A:0.21NS EA NA WA CSA 2898
    rs1460027391,2
    --57920830(+) CTCCCA/GTCTTA 1 -- us2k10--------
    rs1385848551,2
    --57920842(+) CTTCCA/GTGTAG 1 -- us2k10--------
    rs1888811081,2
    --57920888(+) TTCAGC/TTGGGT 1 -- us2k10--------
    rs1412299871,2
    --57920988(+) AAAAAA/GCAGTC 1 -- us2k10--------
    rs342315351,2
    C,F,--57921007(+) TACTGG/AATATC 1 -- us2k13Minor allele frequency- A:0.33NA 6

    HapMap Linkage Disequilibrium report for ZNF17 (57922529 - 57933307 bp)
    Structural Variations (Copy Number Variations, Insertions/Deletions, Inversions)
          Database of Genomic Variants (DGV) variations for ZNF17: --

    SABiosciences Cancer Mutation PCR Assays
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    (in which this Gene is Involved, According to MalaCards, OMIM, UniProtKB, the University of Copenhagen DISEASES database, Novoseek, Genatlas, GeneTests, GAD, HuGE Navigator, and/or TGDB.)
    About This Section

    ZNF17 for disorders           About GeneDecksing

    5 diseases for ZNF17:    About MalaCards
    parainfluenza virus type 3    croup    influenza    choriocarcinoma
    schizophrenia

    1 disease from the University of Copenhagen DISEASES database for ZNF17:
    Croup

    3 Novoseek disease relationships for ZNF17 gene    About this table

    Disease   -log (P-Val)   Hits   PubMed IDs for Articles with Shared Sentences (# sentences)
    parainfluenza 91.2 14 1649512 (1), 11462020 (1), 1328668 (1), 11711635 (1) (see all 13)
    influenza 39.4 2 12477836 (1), 11070006 (1)
    virus infection 9.51 2 8525632 (2)


    Export disorders for ZNF17 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 ZNF17 gene, integrated from 9 sources (see all 23):
    (articles sorted by number of sources associating them with ZNF17)
        Utopia: connect your pdf to the dynamic
    world of online information

    1. Complete sequencing and characterization of 21,243 full-length human cDNAs. (PubMed id 14702039)1, 2 Ota T.... Sugano S. (2004)
    2. The DNA sequence and biology of human chromosome 19. (PubMed id 15057824)1, 2 Grimwood J.... Lucas S.M. (2004)
    3. Prediction of the coding sequences of unidentified human genes. XXII. The complete sequences of 50 new cDNA clones which code for large proteins. (PubMed id 11853319)1, 2 Nagase T.... Ohara O. (2001)
    4. Twenty-seven nonoverlapping zinc finger cDNAs from hu man T cells map to nine different chromosomes with apparent clustering. (PubMed id 2014798)1, 3 Huebner K....Thiesen H.J. (1991)
    5. Multiple genes encoding zinc finger domains are expressed in human T cells. (PubMed id 2288909)1, 2 Thiesen H.-J. (1990)
    6. Human proviral mRNAs down regulated in choriocarcinoma encode a zinc finger protein related to Kruppel. (PubMed id 2115127)1, 3 Kato N.... Cohen M. (1990)
    7. Disrupted in Schizophrenia 1 Interactome: evidence for the close connectivity of risk genes and a potential synaptic basis for schizophrenia. (PubMed id 17043677)1 Camargo L.M....Brandon N.J. (2007)
    8. 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)
    9. Fusion properties of cells infected with human parainfluenza virus type 3: receptor requirements for viral spread and virus-mediated membrane fusion. (PubMed id 1328668)9 Moscona A. and Peluso R.W. (1992)
    10. The use of a quantitative fusion assay to evaluate HN-receptor interaction for human parainfluenza virus type 3. (PubMed id 10603317)9 Levin Perlman S....Moscona A. (1999)

    (in PubMed, OMIM, and NCBI Bookshelf)
    About This Section
     ANDOR
    Aliases
    Disorders
    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: 7565 HGNC: 12958 AceView: ZNF17 Ensembl:ENSG00000186272 euGenes: HUgn7565
    ECgene: ZNF17 H-InvDB: ZNF17

    (According to HUGE)
    About This Section
    HUGE: KIAA1947

    (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 ZNF17 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 ZNF17 gene:
    Search GeneIP for patents involving ZNF17

    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
    Advanced Cell Diagnostics
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    GeneCards Homepage - Last full update: 19 Mar 2013 - Incrementals: 21 Mar 2013 , 15 Apr 2013 , 26 Apr 2013

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    VWF
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    von Willebrand factor
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