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

ZNF711 Gene

protein-coding   GIFtS: 54
GCID: GC0XP084498

zinc finger protein 711

(Previous names: zinc finger protein 6 (CMPX1), zinc finger protein 6 )
(Previous symbol: ZNF6)
 Explore 5 diseases affiliated with
ZNF711 via our new
 Human Malady Compendium 
Biological research products
for ZNF711
    

(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 7111 2     DJ75N13.11
CMPX11 2 3 5     Zinc Finger Protein 6 (CMPX1)1 2
ZNF61 2 3 5     Zinc Finger Protein 61 3
ZNF41 2     MRX972
ZNF51 2     DJ75N13.1 (Znf6-Like)2
Zfp7111 2     

External Ids:    HGNC: 131281   Entrez Gene: 75522   Ensembl: ENSG000001471807   OMIM: 3149905   UniProtKB: Q9Y4623   

Export aliases for ZNF711 gene to outside databases

Previous GC identifers: GC0XP084385 GC0XP078072


(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 ZNF711:
This gene encodes a zinc finger protein of unknown function. It bears similarity to a zinc finger protein which acts as
a transcriptional activator. This gene lies in a region of the X chromosome which has been associated with mental
retardation. (provided by RefSeq, Jul 2008)

UniProtKB/Swiss-Prot: ZN711_HUMAN, Q9Y462
Function: Transcription regulator required for brain development. Probably acts as a transcription factor that binds to
the promoter of target genes and recruits PHF8 histone demethylase, leading to activate expression of genes involved
in neuron development, such as KDM5C




(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_000023.10  NC_018934.1  NT_011651.17  
Regulatory elements:
   SABiosciences Regulatory transcription factor binding sites in the ZNF711 gene promoter:
         E2F-4   E2F-3a   E2F-5   RFX1   GATA-3   E2F-2   GATA-2   GATA-1   E2F   E2F-1   
         Other transcription factors

SwitchGear Promoter luciferase reporter plasmidZNF711 promoter sequence
   Search SABiosciences Chromatin IP Primers for ZNF711

Epigenetics:
QIAGEN PyroMark CpG Assay predesigned Pyrosequencing DNA Methylation assays in human, mouse, rat ZNF711


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

Entrez Gene cytogenetic band: Xq21.1   Ensembl cytogenetic band:  Xq21.1   HGNC cytogenetic band: Xq21.1

ZNF711 Gene in genomic location: bands according to Ensembl, locations according to (and/or Entrez Gene and/or Ensembl if different)
ZNF711 gene location

GeneLoc information about chromosome X         GeneLoc Exon Structure

GeneLoc location for GC0XP084498:  view genomic region     (about GC identifiers)

Start:
84,498,997 bp from pter      End:
84,528,368 bp from pter
Size:
29,372 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: ZN711_HUMAN, Q9Y462 (See protein sequence)
Recommended Name: Zinc finger protein 711  
Size: 761 amino acids; 86245 Da
Subunit: Interacts with PHF8
Subcellular location: Nucleus (Probable)
Sequence caution: Sequence=BAG61766.1; Type=Erroneous initiation; Note=Translation N-terminally extended;
Sequence=CAA39837.2; Type=Frameshift; Positions=Several; Sequence=CAA39837.2; Type=Miscellaneous discrepancy;
Note=Chimera;
Secondary accessions: B4DSV4 Q6NX42 Q9Y4J6
Alternative splicing: 3 isoforms:  Q9Y462-1   Q9Y462-2   Q9Y462-3   (No experimental confirmation available)

Explore the universe of human proteins at neXtProt for ZNF711: NX_Q9Y462

Post-translational modifications:

  • Phosphorylated upon DNA damage, probably by ATM or ATR1
  • View modification sites using PhosphoSitePlus2
  • View neXtProt modification sites for NX_Q9Y462

  • ZNF711 Protein expression data from MOPED and PaxDb:    About this image 
    ZNF711 Protein Expression
    REFSEQ proteins: NP_068838.3  
    ENSEMBL proteins: 
     ENSP00000362260   ENSP00000276123   ENSP00000353922   ENSP00000378798   ENSP00000442071  
    Reactome Protein details: Q9Y462
    Human Recombinant Protein Products for ZNF711: 
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    Uscn Proteins for ZNF711

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

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

    ZNF711 for ontologies           About GeneDecksing



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

    ZNF711 for domains           About GeneDecksing

    4 InterPro domains/families:
     IPR006794 Transcrp_activ_Zfx/Zfy-dom
     IPR015880 Znf_C2H2-like
     IPR013087 Znf_C2H2/integrase_DNA-bd
     IPR007087 Znf_C2H2

    Graphical View of Domain Structure for InterPro Entry Q9Y462

    ProtoNet protein and cluster: Q9Y462

    1 Blocks protein family: IPB006794 Zfx / Zfy transcription activation region

    UniProtKB/Swiss-Prot: ZN711_HUMAN, Q9Y462
    Similarity: Belongs to the krueppel C2H2-type zinc-finger protein family
    Similarity: Contains 12 C2H2-type zinc fingers


    (According to 1UniProtKB, Genatlas, LifeMap Discovery™, IUBMB, and/or 2DME, Human phenotypes from GenomeRNAi, Animal models from MGI Mar 06 2013, inGenious Targeting Laboratory,
    bound targets from SABiosciences, miRNA Gene Targets from miRTarBase, shRNA from OriGene, Sirion Biotech, 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, and Vector BioLabs, Cell Lines from GenScript, LifeMap BioReagents, Sirion Biotech, In Situ Hybridization Assays from Advanced Cell Diagnostics, Ontologies according to Gene Ontology Consortium 01 Mar 2013 via Entrez Gene.)
    About This Section

    Molecular Function:

         UniProtKB/Swiss-Prot Summary: ZN711_HUMAN, Q9Y462
    Function: Transcription regulator required for brain development. Probably acts as a transcription factor that binds to
    the promoter of target genes and recruits PHF8 histone demethylase, leading to activate expression of genes involved
    in neuron development, such as KDM5C

         Gene Ontology (GO): 4 molecular function terms (GO ID links to tree view):    About this table

    GO IDQualified GO termEvidencePubMed IDs
    GO:0003677DNA binding ----
    GO:0005515protein binding IPI--
    GO:0008270zinc ion binding IEA--
    GO:0043565sequence-specific DNA binding IDA--
         
    ZNF711 for ontologies           About GeneDecksing


    Phenotypes:
         4 GenomeRNAi human phenotypes for ZNF711:
     Cell division defect  Decreased POU5F1-GFP protein e  Increased G2M DNA content  Increased number of mitotic ce 

    Animal Models:
       inGenious Targeting Laboratory - Customizable classic, inducible, and humanized mouse model solutions for ZNF711 

    miRNA
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    SwitchGear 3'UTR luciferase reporter plasmidZNF711 3' UTR sequence
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    In Situ Assay
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    (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 ZNF711
        Generic Transcription Pathway
    Gene Expression



    ZNF711 for pathways           About GeneDecksing

    Interactions:

        Search SABiosciences Gene Network CentralTM Interacting Genes and Proteins Networks for ZNF711

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

    1 Interacting protein for ZNF711 (Q9Y4623 ENSP000002761234) via UniProtKB, MINT, STRING, and/or I2D
    InteractantInteraction Details
    GeneCardExternal ID(s)
    PHF8Q9UPP13, ENSP000003388684I2D: score=1 STRING: ENSP00000338868
    About this table

    Gene Ontology (GO): 3 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 ----
    GO:0045893positive regulation of transcription, DNA-dependent IMP--

    ZNF711 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
    Browse Small Molecules at EMD Millipore
    Browse drugs & compounds from Enzo Life Sciences

    Browse Tocris compounds for ZNF711
    Search CenterWatch for drugs/clinical trials and news about ZNF711 / ZN711 

    (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, Sirion Biotech, 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 ZNF711 gene: 
    NM_021998.4  

    Unigene Cluster for ZNF711:

    Zinc finger protein 711
    Hs.326801  [show with all ESTs]
    Unigene Representative Sequence: BX648117
    5 Ensembl transcripts including schematic representations, and UCSC links where relevant:
    ENST00000373165(uc011mqy.1 uc004eeo.3) ENST00000276123 ENST00000360700(uc004eep.3 uc004eeq.3)
    ENST00000395402 ENST00000542798

    miRNA
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    8/30 QIAGEN miScript miRNA Assays for microRNAs that regulate ZNF711 (see all 30):
    hsa-miR-3149 hsa-miR-30c hsa-miR-217 hsa-miR-448 hsa-miR-3607-3p hsa-miR-429 hsa-miR-301a hsa-miR-513c
    SwitchGear 3'UTR luciferase reporter plasmidZNF711 3' UTR sequence
    Inhib. RNA
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      QIAGEN QuantiTect SYBR Green Assays in human, mouse, rat ZNF711
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    Additional cDNA sequence: 

    AK294953.1 AK299604.1 AK299933.1 AK308097.1 AY726603.1 BC006349.2 BC067294.1 BX648117.1 

    7 DOTS entries:

    DT.100672885  DT.100810979  DT.102825354  DT.75120096  DT.97796447  DT.121307078  DT.121307084 

    24/54 AceView cDNA sequences (see all 54):

    BM724321 BC006349 R19445 NM_021998 CB053788 BE675513 AI453159 BX648117 
    AA928817 BU741599 BC067294 BI524105 BM979874 T16534 BP379715 BM669821 
    AI479353 AA331768 CB962230 BM975110 R44692 BI598126 BF203844 AI989555 

    GeneLoc Exon Structure

    5/9 Alternative Splicing Database (ASD) splice patterns (SP) for ZNF711 (see all 9)    About this scheme

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


    ECgene alternative splicing isoforms for ZNF711

    (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

    ZNF711 expression in normal human tissues (normalized intensities)
    See probesets specificity/sensitivity at GeneAnnot
    About this imageBioGPS
    CGAP TAG: CTATATTGTG
    ZNF711 Expression
    About this image
    See ZNF711 Protein Expression from SPIRE MOPED and PaxDB
    Genevestigator expression for ZNF711

    SOURCE GeneReport for Unigene cluster: Hs.326801

    UniProtKB/Swiss-Prot: ZN711_HUMAN, Q9Y462
    Tissue specificity: Expressed in neural tissues

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    In Situ
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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 chordates.

    Orthologs for ZNF711 gene from 3/10 species (see all 10)    About this table
    Organism Taxonomic
    classification
    Gene Description Human
    Similarity
    Orthology
    Type
    Details
    chicken
    (Gallus gallus)
    Aves ZNF7111 zinc finger protein 711 80.67(n)
    86.39(a)
      422269  XM_420253.3  XP_420253.3 
    lizard
    (Anolis carolinensis)
    Reptilia ZNF7116
    --
    80(a)
    1 ↔ 1
    GL343202.1(1114013-1127544)
    zebrafish
    (Danio rerio)
    Actinopterygii znf7111 zinc finger protein 711 67.89(n)
    73.26(a)
      562505  NM_001105523.1  NP_001098993.1 


    ENSEMBL Gene Tree for ZNF711 (if available)
    TreeFam Gene Tree for ZNF711 (if available) 

    (Paralogs according to 1HomoloGene,
    2Ensembl, and 3SIMAP, Pseudogenes according to 4Pseudogene.org Build 68)
    About This Section
    Paralogs for ZNF711 gene
    ZNF6392  ZFY2  ZFX2  
    18/101 SIMAP similar genes for ZNF711 using alignment to 4 protein entries:     ZN711_HUMAN (see all proteins) (see all similar genes):
    ZFY    ZFX    ZNF55    kr-znf3    HZF16    KLF4
    ZBTB17    ZNF    ZNF672    A-328A3.4    ZFS-2    ZFS-5
    ZNF500    HZF36    ZNF410    ZSCAN21    DKFZp686N0199    KLF1

    ZNF711 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

    10/340 NCBI SNPs in ZNF711 are shown (see all 340    About this table
    Genomic DataTranscription Related DataAllele Frequencies
    SNP IDValidClinical
    significance
    Chr X posSequence#AA
    Chg
    TypeMore#Allele
    freq
    PopTotal
    sample
    More
    ----------
    rs1994222401,2
    Cpathogenic84526121(+) ATATGA/TGAACC 2 R * stg10--------
    rs20668961,2
    C--84497027(+) CTGAAA/C/GAAGGT 1 -- us2k11CSA 1
    rs1415178401,2
    --84497092(+) CTCAGG/TATATT 1 -- us2k10--------
    rs1812790811,2
    --84497784(+) TATCTA/GTCTAT 1 -- us2k10--------
    rs1854830341,2
    --84497813(+) TAGTAA/GTAACT 1 -- us2k10--------
    rs1898747981,2
    --84497849(+) AATTAC/TATCTC 1 -- us2k10--------
    rs21066661,2
    C,F,A--84497905(+) CAGAGC/GAGAGT 1 -- us2k13Minor allele frequency- G:0.33NA WA 6
    rs10066291,2
    C,F,A,H--84497935(+) TAGCCC/TTCAAA 1 -- us2k113Minor allele frequency- T:0.13NS EA NA WA 1688
    rs1442257231,2
    --84498015(+) TTTGCC/TGACTC 1 -- us2k10--------
    rs1823458761,2
    --84498401(+) AGCTGA/TAAGTG 1 -- us2k10--------

    HapMap Linkage Disequilibrium report for ZNF711 (84498997 - 84528368 bp)
    Structural Variations (Copy Number Variations, Insertions/Deletions, Inversions)
    Database of Genomic Variants (DGV): 1 variation for ZNF711
         1 CNV: 103261
    Human Gene Mutation Database (HGMD): ZNF711

    Locus Specific Mutation Databases (LSDB): ZNF711

    SABiosciences Cancer Mutation PCR Assays
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    DNA2.0 Custom Variant and Variant Library Synthesis for ZNF711

    (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

    ZNF711 for disorders           About GeneDecksing

    OMIM gene information: 314990    OMIM disorders: --

    UniProtKB/Swiss-Prot: ZN711_HUMAN, Q9Y462
  • Defects in ZNF711 are the cause of mental retardation X-linked ZNF711-related (MRXZ) [MIM:300803]. Mental
  • retardation is characterized by significantly below average general intellectual functioning associated with
    impairments in adaptative behavior and manifested during the developmental period

    5 diseases for ZNF711:    About MalaCards
    allan-herndon-dudley syndrome    mental retardation, x-linked    autism spectrum disorder    intellectual disability
    neuronitis

    1 disease from the University of Copenhagen DISEASES database for ZNF711:
    Allan-Herndon-Dudley syndrome

    Export disorders for ZNF711 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 ZNF711 gene, integrated from 9 sources (see all 14):
    (articles sorted by number of sources associating them with ZNF711)
        Utopia: connect your pdf to the dynamic
    world of online information

    1. A functional link between the histone demethylase PHF 8 and the transcription factor ZNF711 in X-linked mental retardation. (PubMed id 20346720)1, 2 Kleine-Kohlbrecher D....Helin K. (2010)
    2. The DNA sequence of the human X chromosome. (PubMed id 15772651)1, 2 Ross M.T.... Bentley D.R. (2005)
    3. 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)
    4. An X linked zinc finger gene mapping to Xq21.1-q21.3 closely related to ZFX and ZFY. Possible origins from a common ancestral gene. (PubMed id 1923752)1, 2 Lloyd S.L....Affara N.A. (1991)
    5. Fine mapping of Xq11.1-q21.33 and mutation screening of RPS6KA6, ZNF711, ACSL4, DLG3, and IL1RAPL2 for autism spectrum disorders (AS D). (PubMed id 21384559)1 KantojAorvi K....JAorvelAo I. (2011)
    6. A proteome-wide, quantitative survey of in vivo ubiqui tylation sites reveals widespread regulatory roles. (PubMed id 21890473)1 Wagner S.A....Choudhary C. (2011)
    7. A systematic, large-scale resequencing screen of X-chromosome coding exons in mental retardation. (PubMed id 19377476)2 Tarpey P.S.... Stratton M.R. (2009)
    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. Complete sequencing and characterization of 21,243 full-length human cDNAs. (PubMed id 14702039)2 Ota T.... Sugano S. (2004)
    10. Sumoylation of heterogeneous nuclear ribonucleoproteins, zinc finger proteins, and nuclear pore complex proteins: a proteomic analysis. (PubMed id 15161980)1 Li T....Chock P.B. (2004)

    (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: 7552 HGNC: 13128 AceView: ZNF6 Ensembl:ENSG00000147180 euGenes: HUgn7552
    ECgene: ZNF711 H-InvDB: ZNF711

    (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 ZNF711 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 ZNF711 gene:
    Search GeneIP for patents involving ZNF711

    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: 19 Mar 2013 - Incrementals: 21 Mar 2013 , 15 Apr 2013 , 26 Apr 2013 , 13 May 2013

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