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

ZNF711 Gene

protein-coding   GIFtS: 57
GCID: GC0XP084498

Zinc Finger Protein 711

(Previous names: zinc finger protein 6 (CMPX1), zinc finger protein 6)
(Previous symbol: ZNF6)
  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

Aliases
Zinc Finger Protein 7111 2     ZNF42
ZNF61 2 3 5     ZNF52
CMPX12 3 5     Zfp7112
Zinc Finger Protein 6 (CMPX1)1 2     dJ75N13.12
Zinc Finger Protein 61 3     DJ75N13.1 (Znf6-Like)2
MRX972     

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 Gene:
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)

GeneCards Summary for ZNF711 Gene: 
ZNF711 (zinc finger protein 711) is a protein-coding gene. Diseases associated with ZNF711 include allan-herndon-dudley syndrome, and znf711-related x-linked mental retardation, and among its related super-pathways are Gene Expression. GO annotations related to this gene include sequence-specific DNA binding and zinc ion binding. An important paralog of this gene is ZNF639.

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 73), Regulatory elements and Epigenetics data according to QIAGEN, SABiosciences, and/or SwitchGear Genomics)
About This Section
RefSeq DNA sequence:
NC_000023.10  NT_011651.17  NC_018934.2  
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 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: 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

Explore proteomics data for ZNF711 at MOPED 

Post-translational modifications:

  • View modification sites using PhosphoSitePlus
  • View neXtProt modification sites for NX_Q9Y462

  • ZNF711 Protein expression data from MOPED1, PaxDb2 and MAXQB3 :    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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    Cloud-Clone Corp. 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 HGNC, IUPHAR, InterPro, ProtoNet, UniProtKB, and/or BLOCKS, Sets of similar genes according to GeneDecks)
    About This Section
    HGNC Gene Families: 
    ZNF: Zinc fingers, C2H2-type

    4 InterPro protein domains:
     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 domain: 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


    ZNF711 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: 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): 5 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 ----
    GO:0043565sequence-specific DNA binding IDA--
    GO:0046872metal ion binding IEA--
         
    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:
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    SwitchGear 3'UTR luciferase reporter plasmidZNF711 3' UTR sequence
    Inhib. RNA
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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 ZNF711 About                                                                                                See pathways by source

    SuperPathContained pathways About
    1Generic Transcription Pathway
    Generic Transcription Pathway0.47
    Gene Expression0.47

    Pathways by source                                                                                                                                                                 See SuperPaths
    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, 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 ZNF711 (ZN711)

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

    (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 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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    SwitchGear 3'UTR luciferase reporter plasmidZNF711 3' UTR sequence
    Inhib. RNA
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    Additional mRNA 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):

    CB053788 AI453159 NM_021998 BX648117 T16534 BU741599 R19445 BE675513 
    BM724321 BM979874 BI524105 BC006349 BC067294 AA928817 BP379715 AI989555 
    AA897714 BM975110 BF055342 AI678955 BI598126 BF203844 AL696495 CB962230 

    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)      ZNF711 embryonic expression: see
    See probesets specificity/sensitivity at GeneAnnot
    About this imageBioGPS <intensity>2/3
    CGAP TAG: CTATATTGTG
    ZNF711 Expression
    About this image


    ZNF711 expression in embryonic tissues and stem cells    About this table
    Data from LifeMap, the Embryonic Development and Stem Cells Database 
     5/8 selected tissues (see all 8) fully expand
     
     Blood (Hematopoietic System)    fully expand to see all 2 entries
             Hematopoietic Stem Cells Hematopoietic Bone Marrow
     
     Heart (Cardiovascular System)
             Cardiac Fibroblasts Myocardium
     
     Ovary (Reproductive System)
             XX Germ Cells Ovigerous Cord
     
     Liver (Hepatobiliary System)
             Mesothelial Cells Hepatic Mesenchyme
     
     Gonad
             XX Germ Cells Ovigerous Cord

    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

        SABiosciences Custom PCR Arrays for ZNF711
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    In Situ
    Assay Products:
     

     
    Advanced Cell Diagnostics RNAscope RNA in situ hybridization assays for ZNF711

    (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 4/10 species (see all 10)    About this table
    Organism Taxonomic
    classification
    Gene Description Human
    Similarity
    Orthology
    Type
    Details
    mouse
    (Mus musculus)
    Mammalia Zfp7111 , 5 zinc finger protein 7111, 5 92.29(n)1
    96.32(a)1
      X (48.76 cM)5
    2455951  NM_177747.31  NP_808415.21 
     1126005265 
    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
    zinc finger protein 711
    81(a)
    1 ↔ 1
    GL343202.1(1113841-1128927)
    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  
    18/84 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, 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

    10/423 SNPs in ZNF711 are shown (see all 423)    About this table     
    Genomic DataTranscription Related DataAllele Frequencies
    SNP IDValidClinical
    significance
    Chr X posSequence#AA
    Chg
    TypeMore#Allele
    freq
    PopTotal
    sample
    More
    ----------
    rs1994222401,2
    Cpathogenic184500100(+) ATATGA/TGAACC 2 R * stg10--------
    VAR_0629944
    ----see VAR_0629942 N S mis40--------
    VAR_0629914
    ----see VAR_0629912 T A mis40--------
    VAR_0629954
    ----see VAR_0629952 E D mis40--------
    VAR_0629934
    ----see VAR_0629932 M T mis40--------
    VAR_0629904
    ----see VAR_0629902 G E mis40--------
    VAR_0629924
    ----see VAR_0629922 H R mis40--------
    rs20668961,2
    C,F--84471222(+) CTGAAA/C/GAAGGT 1 -- us2k11CSA 1
    rs1415178401,2
    C--84471287(+) CTCAGG/TATATT 1 -- us2k10--------
    rs1812790811,2
    --84471979(+) TATCTA/GTCTAT 1 -- us2k10--------

    HapMap Linkage Disequilibrium report for ZNF711 (84498997 - 84528368 bp)

    Structural Variations
         Database of Genomic Variants (DGV) 2 variations for ZNF711:    About this table     
    Variant IDTypeSubtypePubMed ID
    esv2466752CNV Deletion19546169
    esv2740275CNV Deletion23290073


    Human Gene Mutation Database (HGMD): ZNF711

    Locus Specific Mutation Databases (LSDB): ZNF711
    SABiosciences Cancer Mutation PCR Assays
    SeqTarget long-range PCR primers for resequencing ZNF711
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    (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: 314990    OMIM disorders: --

    UniProtKB/Swiss-Prot: ZN711_HUMAN, Q9Y462
  • Mental retardation, X-linked, ZNF711-related (MRXZ) [MIM:300803]: A disorder characterized by
    significantly below average general intellectual functioning associated with impairments in adaptative behavior
    and manifested during the developmental period. Note=The disease is caused by mutations affecting the gene
    represented in this entry

  • 7 diseases for ZNF711:    About MalaCards
    allan-herndon-dudley syndrome    znf711-related x-linked mental retardation    autism spectrum disorder    intellectual disability
    mental retardation    mental retardation, x-linked    neuronitis

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

    ZNF711 for disorders           About GeneDecksing


    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)
    About This Section
     ANDOR
    Aliases
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      Query String
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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: 23 Oct 2013 - Incrementals: 3 Nov 2013 , 7 Nov 2013 , 23 Jan 2014

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