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ZNF778 Gene

protein-coding   GIFtS: 52
GCID: GC16P089284

Zinc Finger Protein 778

  See ZNF778-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)
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Aliases
Zinc Finger Protein 7781 2

External Ids:    HGNC: 264791   Entrez Gene: 1973202   Ensembl: ENSG000001701007   UniProtKB: Q96MU63   

Export aliases for ZNF778 gene to outside databases

Previous GC identifers: GC16P087812 GC16P074983


(According to Entrez Gene, GeneCards, Tocris Bioscience, Wikipedia's Gene Wiki, PharmGKB,
UniProtKB/Swiss-Prot, and/or UniProtKB/TrEMBL)
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Entrez Gene summary for ZNF778 Gene:
The protein encoded by this gene is a member of the krueppel C2H2-type zinc-finger protein family, and it contains
one KRAB domain and eighteen C2H2-type zinc fingers. This gene is a candidate gene for autism and variable
cognitive impairment in the 16q24.3 microdeletion syndrome. Alternatively spliced transcript variants have been
found for this gene. (provided by RefSeq, Jan 2011)

GeneCards Summary for ZNF778 Gene:
ZNF778 (zinc finger protein 778) is a protein-coding gene. Diseases associated with ZNF778 include kbg syndrome, and 16q24.3 microdeletion syndrome. An important paralog of this gene is ZNF812.

UniProtKB/Swiss-Prot: ZN778_HUMAN, Q96MU6
Function: May be involved in transcriptional regulation (By similarity)




(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 75), Regulatory elements and Epigenetics data according to QIAGEN, and/or SwitchGear Genomics)
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RefSeq DNA sequence at NCBI GenBank:
NC_000016.9  NT_010498.16  NC_018927.2  
Regulatory elements:
   Search for regulatory transcription factor binding sites for ZNF778
         Other transcription factors

SwitchGear Promoter luciferase reporter plasmidZNF778 promoter sequence
   Search Chromatin IP Primers for ZNF778

Epigenetics:
DNA Methylation CpG Assay Predesigned for Pyrosequencing in human, mouse, rat ZNF778


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

Entrez Gene cytogenetic band: 16q24.3   Ensembl cytogenetic band:  16q24.3   HGNC cytogenetic band: 16q24.3

ZNF778 Gene in genomic location: bands according to Ensembl, locations according to (and/or Entrez Gene and/or Ensembl if different)
ZNF778 gene location

GeneLoc information about chromosome 16         GeneLoc Exon Structure

GeneLoc location for GC16P089284:  view genomic region     (about GC identifiers)

Start:
89,284,111 bp from pter      End:
89,295,965 bp from pter
Size:
11,855 bases      Orientation:
plus strand

(According to 1UniProtKB, HORDE, 2neXtProt, Ensembl, and/or Reactome, Modification sites according to PhosphoSitePlus, Specific Peptides from DME, 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, Cloud-Clone Corp., and/or eBioscience,
Biochemical Assays by EMD Millipore, R&D Systems, OriGene, GenScript, Cell Signaling Technology, Enzo Life Sciences, Cloud-Clone Corp., and/or eBioscience, Antibodies by EMD Millipore, R&D Systems, Cell Signaling Technology, OriGene, Novus Biologicals, Thermo Fisher Scientific, LSBio, Abcam, Cloud-Clone Corp, and/or others.)
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UniProtKB/Swiss-Prot: ZN778_HUMAN, Q96MU6 (See protein sequence)
Recommended Name: Zinc finger protein 778  
Size: 729 amino acids; 81964 Da
Sequence caution: Sequence=BAB71183.1; Type=Frameshift; Positions=393;
Secondary accessions: Q08AG0
Alternative splicing: 2 isoforms:  Q96MU6-1   Q96MU6-2   

Explore the universe of human proteins at neXtProt for ZNF778: NX_Q96MU6

Explore proteomics data for ZNF778 at MOPED

Post-translational modifications: 

  • Modification sites at neXtProt
  • Modification sites at PhosphoSitePlus

  • See ZNF778 Protein Expression from SPIRE MOPED, PaxDB, and MaxQB

    REFSEQ proteins (2 alternative transcripts): 
    NP_001188336.1  NP_872337.2  

    ENSEMBL proteins: 
     ENSP00000457800   ENSP00000405289   ENSP00000456655   ENSP00000305203  
    Reactome Protein details: Q96MU6

    ZNF778 Human Recombinant Protein Products:

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    Cloud-Clone Corp. Proteins for ZNF778

     
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    (According to HGNC, IUPHAR, InterPro, ProtoNet, UniProtKB, and/or BLOCKS, Sets of similar genes according to GeneDecks)
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    HGNC Gene Families:
    ZNF: Zinc fingers, C2H2-type

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

    Graphical View of Domain Structure for InterPro Entry Q96MU6

    ProtoNet protein and cluster: Q96MU6

    1 Blocks protein domain: IPB001909 KRAB box

    UniProtKB/Swiss-Prot: ZN778_HUMAN, Q96MU6
    Similarity: Belongs to the krueppel C2H2-type zinc-finger protein family
    Similarity: Contains 18 C2H2-type zinc fingers
    Similarity: Contains 1 KRAB domain


    Find genes that share domains with ZNF778           About GenesLikeMe


    (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,
    transcription factor targeting from QIAGEN and/or HOMER, miRNA Gene Targets from miRTarBase, shRNA from OriGene, siRNAs from OriGene, QIAGEN, microRNA from QIAGEN, SwitchGear Genomics, Gene Editing from DNA2.0, Clones from OriGene, GenScript, Sino Biological, DNA2.0, Vector BioLabs and/or Addgene, Cell Lines from GenScript, ESI BIO, In Situ Hybridization Assays from Advanced Cell Diagnostics, Flow cytometry from eBioscience, Ontologies according to Gene Ontology Consortium 01 Apr 2014 via Entrez Gene.)
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    Molecular Function:

         UniProtKB/Swiss-Prot Summary: ZN778_HUMAN, Q96MU6
    Function: May be involved in transcriptional regulation (By similarity)

         Gene Ontology (GO): 3 molecular function terms:    About this table

    GO IDQualified GO termEvidencePubMed IDs
    GO:0003676nucleic acid binding ----
    GO:0003677DNA binding IEA--
    GO:0046872metal ion binding IEA--
         
    Find genes that share ontologies with ZNF778           About GenesLikeMe


    Phenotypes:
         1 GenomeRNAi human phenotype for ZNF778:
     Increased HPV18 LCR reporter a 

    Animal Models:
       inGenious Targeting Laboratory: Let us create your new Knockout/Knockin mouse model for ZNF778
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       genOway customized Knockin model: humanization, point mutation, expression monitoring, etc. for ZNF778

    miRNA
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    miRTarBase miRNAs that target ZNF778:
    hsa-mir-27a-3p (MIRT050018)

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    SwitchGear 3'UTR luciferase reporter plasmidZNF778 3' UTR sequence
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    Predesigned siRNA for gene silencing in human, mouse, rat ZNF778

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    Advanced Cell Diagnostics RNAscope RNA in situ hybridization assays for ZNF778


    (According to UniProtKB, COMPARTMENTS Subcellular localization database, Ontologies according to Gene Ontology Consortium 01 Apr 2014 via Entrez Gene.)
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    Subcellular locations from UniProtKB/Swiss-Prot
    ZN778_HUMAN, Q96MU6: Nucleus (Probable)
    Subcellular locations from COMPARTMENTS: 

    CompartmentConfidence
    nucleus4
    cytosol2

    Gene Ontology (GO): 2 cellular component terms:    About this table

    GO IDQualified GO termEvidencePubMed IDs
    GO:0005622intracellular ----
    GO:0005634nucleus IEA--

    Find genes that share ontologies with ZNF778           About GenesLikeMe


    (SuperPaths according to PathCards, Pathways according to 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 QIAGEN, 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 Apr 2014 via Entrez Gene).
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    SuperPaths for ZNF778 About    
    See pathways by source

    SuperPathContained pathways About
    1Gene Expression
    Generic Transcription Pathway0.40
    Gene Expression0.40


    Find genes that share SuperPaths with ZNF778           About GenesLikeMe

    Pathways by source                                                                                                                                                                 See SuperPaths
    Show all pathways


    1 Reactome Pathway for ZNF778
        Generic Transcription Pathway


        Custom Pathway & Disease-focused RT2 Profiler PCR Arrays for ZNF778
    Interactions:

        Search GeneGlobe Interaction Network for ZNF778

    STRING Interaction Network Preview (showing 2 interactants - click image to see more details)

    2 Interacting proteins for ZNF778 (ENSP000004052894) via UniProtKB, MINT, STRING, and/or I2D
    InteractantInteraction Details
    GeneCardExternal ID(s)
    SOS2ENSP000002163734STRING: ENSP00000216373
    SOS1ENSP000003846754STRING: ENSP00000384675
    About this table

    Gene Ontology (GO): 2 biological process terms:    About this table

    GO IDQualified GO termEvidencePubMed IDs
    GO:0006351transcription, DNA-templated IEA--
    GO:0006355regulation of transcription, DNA-templated IEA--

    Find genes that share ontologies with ZNF778           About GenesLikeMe



    (Chemical Compounds according to UniProtKB, Enzo Life Sciences, EMD Millipore, Tocris Bioscience, ApexBio, HMDB, BitterDB, and/or Novoseek, Ligands according to IUPHAR, and Drugs according to DrugBank, Enzo Life Sciences, and/or PharmGKB)
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    Browse Small Molecules at EMD Millipore
       Browse drugs & compounds from Enzo Life Sciences
      Browse compounds at ApexBio 

    Browse Tocris compounds for ZNF778 (ZN778)



    (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,
    exon structure from GeneLoc, alternative splicing isoforms according to ASD and/or ECgene,
    siRNAs from OriGene, QIAGEN, shRNA from OriGene, microRNA from QIAGEN, SwitchGear Genomics,
    Tagged/untagged cDNA clones from OriGene, GenScript, DNA2.0, Vector BioLabs, and/or Addgene, Primers from OriGene, and/or QIAGEN, Flow cytometry from eBioscience )
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    REFSEQ mRNAs for ZNF778 gene (2 alternative transcripts): 
    NM_001201407.1  NM_182531.3  

    Unigene Cluster for ZNF778:

    Zinc finger protein 778
    Hs.647385  [show with all ESTs]
    Unigene Representative Sequence: NM_001201407
    6 Ensembl transcripts including schematic representations, and UCSC links where relevant:
    ENST00000565877 ENST00000564906 ENST00000433976(uc021tms.1 uc010vpg.2 uc002fmv.3 uc002fmw.2)
    ENST00000567651 ENST00000306502 ENST00000565414
    miRNA
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    Primer
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      QuantiTect SYBR Green Assays in human, mouse, rat ZNF778
      QuantiFast Probe-based Assays in human, mouse, rat ZNF778

    Additional mRNA sequence: 

    AK056437.1 BC015872.1 BC125192.1 BC143524.1 NR_037705.1 

    2 DOTS entries:

    DT.40209848  DT.75123045 

    15 AceView cDNA sequences:

    BU608778 BF035326 BC015872 BM697683 BG563705 AK056437 NM_182531 BU735850 
    W95097 BI669263 W95098 BM147023 BF095126 BQ219517 BF964392 

    GeneLoc Exon Structure

    3 Alternative Splicing Database (ASD) splice patterns (SP) for ZNF778    About this scheme

    ExUns: 1a · 1b ^ 2a · 2b ^ 3 ^ 4 ^ 5 ^ 6 ^ 7
    SP1:                                      -               
    SP2:                                                      
    SP3:              -                                       


    ECgene alternative splicing isoforms for ZNF778

    (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™, Protein expression images according to data from SPIRE 1MOPED, 2PaxDb, and 3MaxQB, plus additional links to SOURCE, and/or BioGPS, and/or UniProtKB,
    PCR Arrays from QIAGEN, Primers from OriGene, and/or QIAGEN, In Situ Hybridization Assays from Advanced Cell Diagnostics)
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    ZNF778 expression in normal human tissues (normalized intensities)
    See probesets specificity/sensitivity at GeneAnnot
    About this imageBioGPS <intensity>2/3
    CGAP TAG: TGAAAACTCA
    ZNF778 Expression
    About this image


    ZNF778 expression in embryonic tissues and stem cells    About this table
    Data from LifeMap, the Embryonic Development and Stem Cells Database
     selected tissues (see all 2) fully expand
     
     Neurons
             nGnG Amacrine Cells Inner Nuclear Layer
     
     Eye (Sensory Organs)
             nGnG Amacrine Cells Inner Nuclear Layer
    ZNF778 Protein expression data from MOPED1, PaxDb2 and MaxQB3    About this image

    ZNF778 Protein Expression

    SOURCE GeneReport for Unigene cluster: Hs.647385
        Custom PCR Arrays for ZNF778
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    In Situ
    Assay Products:
     

     
    Advanced Cell Diagnostics RNAscope RNA in situ hybridization assays for ZNF778

    (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)
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    This gene was present in the common ancestor of chordates.

    Orthologs for ZNF778 gene from Selected species (see all 5)    About this table
    Organism Taxonomic
    classification
    Gene Description Human
    Similarity
    Orthology
    Type
    Details
    mouse
    (Mus musculus)
    Mammalia Zfp5605
    Zfp261
    zinc finger protein 5605
    zinc finger protein 261
    65.03(n)1
    53.02(a)1
      9 (7.52 cM)5
    226881  NM_011753.31  NP_035883.21 
     203451365 
    rainbow trout
    (Oncorhynchus mykiss)
    Actinopterygii BX867429.12   -- 75.42(n)    BX867429.1 


    ENSEMBL Gene Tree for ZNF778 (if available)
    TreeFam Gene Tree for ZNF778 (if available)

    (Paralogs according to 1HomoloGene,
    2Ensembl, and 3SIMAP, Pseudogenes according to 4Pseudogene.org Build 68)
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    Paralogs for ZNF778 gene
    ZNF8122  ZNF2662  ZNF4262  ZNF5602  ZNF8462  ZNF1212  ZNF5612  ZNF5592  
    ZNF5622  
    Selected SIMAP similar genes for ZNF778 using alignment to 4 protein entries:     ZN778_HUMAN (see all proteins) (see all similar genes):
    ZNF625-ZNF20    FIK    MGC12518    ZNF738    ZNF669    LOC101928664
    ZNF177    ZFP90    ZNF121    ZNF78L1    ZNF506    KRBOX4
    ZNF84    ZNF577    ZNF302    ZNF846    ZNF675    ZNF624

    Find genes that share paralogs with ZNF778           About GenesLikeMe



    (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), the Human Cytochrome P450 Allele Nomenclature Database, and the Locus Specific Mutation Databases (LSDB), Blood group antigen gene mutations by BGMUT, Resequencing Primers, Cancer Mutation PCR Arrays and Assays, and Copy Number PCR Arrays from QIAGEN)
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    Selected SNPs for ZNF778 (see all 617)    About this table                                 

    Genomic DataTranscription Related DataAllele Frequencies
    SNP IDValidClinical
    significance
    Chr 16 posSequence#AA
    Chg
    TypeMore#Allele
    freq
    PopTotal
    sample
    More
    ----------
    rs724919481,2
    C--74995446(+) GCAGCA/GTAGGC 3 -- ds50010--------
    rs1486788221,2
    --74995450(+) CGTAGA/GCTCTG 3 -- ds50010--------
    rs1826196441,2
    --74995451(+) GTAGGC/GTCTGG 3 -- ds50010--------
    rs1869023871,2
    --74995453(+) AGGCTC/TTGGTT 3 -- ds50010--------
    rs347387671,2
    C--89285591(+) CAACA-/TTTTTC 3 -- int10--------
    rs105865251,2
    C,F--89287614(+) TACACAG/-TGTGT 3 -- int12Minor allele frequency- -:0.50NA CSA 4
    rs756379551,2
    --89287614(+) TACACT/AGTGTG 3 -- int11Minor allele frequency- A:0.50NA 2
    rs1123021111,2
    C--89287990(+) ATGGC-/CT/TG 
            
    TGTGT
    3 -- int11CSA 2
    rs664781571,2
    C--89287992(+) ATGGC-/TGTG  
            
    TGTGT
    3 -- int10--------
    rs355033851,2
    C--89287993(+) GTGTG-/GTTGTGT 3 -- int11Minor allele frequency- GT:0.00NA 2

    HapMap Linkage Disequilibrium report for ZNF778 (89284111 - 89295965 bp)

    Structural Variations
         Database of Genomic Variants (DGV) Selected variations for ZNF778 (see all 15):    About this table    
    Variant IDTypeSubtypePubMed ID
    esv2665882CNV Deletion23128226
    esv1006131CNV Deletion20482838
    nsv509638CNV Insertion20534489
    esv268384CNV Insertion20981092
    nsv907394CNV Loss21882294
    nsv907357CNV Loss21882294
    dgv3006n71CNV Loss21882294
    dgv2998n71CNV Loss21882294
    nsv457622CNV Loss19166990
    dgv3004n71CNV Loss21882294

    Human Gene Mutation Database (HGMD): ZNF778
    Site Specific Mutation Identification with PCR Assays
    2 Copy Number PCR Panels containing ZNF778:
    Birth Defects
    Intellectual Disability
    SeqTarget long-range PCR primers for resequencing ZNF778
    DNA2.0 Custom Variant and Variant Library Synthesis for ZNF778

    (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.)
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    2 diseases for ZNF778:    
    About MalaCards
    kbg syndrome    16q24.3 microdeletion syndrome

    1 disease from the University of Copenhagen DISEASES database for ZNF778:
    KBG syndrome

    Find genes that share disorders with ZNF778           About GenesLikeMe

    Genetic Association Database (GAD): ZNF778

    Export disorders for ZNF778 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)
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    PubMed articles for ZNF778 gene integrated from 10 sources:
    (articles sorted by number of sources associating them with ZNF778)
        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. (Genome Res. 2004)
    2. Complete sequencing and characterization of 21,243 full-length human cDNAs. (PubMed id 14702039)1, 2 Ota T.... Sugano S. (Nat. Genet. 2004)
    3. Methods for quantification of in vivo changes in protein ubiquitination following proteasome and deubiquitinase inhibition. (PubMed id 22505724)1 Udeshi N.D....Carr S.A. (amp 2012)
    4. Identification of ANKRD11 and ZNF778 as candidate genes for autism and variable cognitive impairment in the novel 16q24.3 microdeletion syndrome. (PubMed id 19920853)1 Willemsen M.H....Kleefstra T. (Eur. J. Hum. Genet. 2010)
    5. A germline-specific class of small RNAs binds mammalian Piwi proteins. (PubMed id 16751776)1 Girard A....Carmell M.A. (Nature 2006)
    6. Diversification of transcriptional modulation: large-scale identification and characterization of putative alternative promoters of human genes. (PubMed id 16344560)1 Kimura K.... Sugano S. (Genome Res. 2006)
    7. The sequence and analysis of duplication-rich human chromosome 16. (PubMed id 15616553)2 Martin J.... Pennacchio L.A. (Nature 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. (Proc. Natl. Acad. Sci. U.S.A. 2002)
    9. The sequence of the human genome. (PubMed id 11181995)1 Venter J.C.... Zhu X. (Science 2001)

    (in PubMed, OMIM, and NCBI Bookshelf)
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     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)
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    Entrez Gene: 197320 HGNC: 26479 AceView: FLJ31875 Ensembl:ENSG00000170100 euGenes: HUgn197320
    ECgene: ZNF778 H-InvDB: ZNF778

    (According to HUGE)
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      --

    (According to PharmGKB, ATLAS, HORDE, IMGT, LEIDEN, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL, and/or others, e.g. Wikipedia and GeneReviews, via UniProtKB/Swiss-Prot)
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    NameDescription
    PharmGKB entry for ZNF778 Pharmacogenomics, SNPs, Pathways

    (Patent information from GeneIP,
    Licensable technologies from WIS Yeda, Salk, Tufts,
    IP news from LifeMap Sciences, Inc.)
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    Patent Information for ZNF778 gene:
    Search GeneIP for patents involving ZNF778

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



    (Antibodies, recombinant proteins, and assays from EMD Millipore, R&D Systems, OriGene, QIAGEN, GenScript, Cell Signaling Technology, Novus Biologicals, Sino Biological, Enzo Life Sciences, Abcam, ProSpec, Cloud-Clone Corp., Thermo Fisher Scientific, LSBio, eBioscience, and/or others, Gene Editing from DNA2.0. Clones from OriGene, GenScript, Sino Biological, DNA2.0, SwitchGear Genomics, Vector BioLabs, Addgene, Cell lines from GenScript, and ESI BIO, Flow cytometery from eBioscience, PCR Arrays from QIAGEN, Drugs and/or compounds from EMD Millipore, Tocris Bioscience, Enzo Life Sciences, and/or ApexBio, In Situ Hybridization Assays from
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