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ZNF92 Gene

protein-coding   GIFtS: 56
GCID: GC07P064838

Zinc Finger Protein 92

(Previous name: zinc finger protein 92 (HTF12))
  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)
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Aliases
Zinc Finger Protein 921 2     HPF122
Zinc Finger Protein HTF122 3     HTF122
Zinc Finger Protein 92 (HTF12)1     TF122
HEL-2032     Epididymis Luminal Protein 2032

External Ids:    HGNC: 131681   Entrez Gene: 1683742   Ensembl: ENSG000001467577   OMIM: 6039745   UniProtKB: Q039363   

Export aliases for ZNF92 gene to outside databases

Previous GC identifers: GC19U990112 GC07P064236 GC07P064250 GC07P064282 GC07P064476 GC07P061127


(According to Entrez Gene, GeneCards, Tocris Bioscience, Wikipedia's Gene Wiki, PharmGKB,
UniProtKB/Swiss-Prot, and/or UniProtKB/TrEMBL)
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GeneCards Summary for ZNF92 Gene:
ZNF92 (zinc finger protein 92) is a protein-coding gene. Diseases associated with ZNF92 include myocardial stunning, and retinitis. GO annotations related to this gene include sequence-specific DNA binding transcription factor activity. An important paralog of this gene is ZNF85.

UniProtKB/Swiss-Prot: ZNF92_HUMAN, Q03936
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 75), Regulatory elements and Epigenetics data according to QIAGEN, and/or SwitchGear Genomics)
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RefSeq DNA sequence:
NC_000007.14  NT_007933.16  NC_018918.2  
Regulatory elements:
   Regulatory transcription factor binding sites in the ZNF92 gene promoter:
         STAT5B   NF-YA   NF-YB   CBF-B   CBF-A   Ik-2   IRF-7A   CP1A   NF-Y   CBF(2)   
         Other transcription factors

SwitchGear Promoter luciferase reporter plasmids (see all 2): ZNF92 promoter sequence
   Search Chromatin IP Primers for ZNF92

Epigenetics:
DNA Methylation CpG Assay Predesigned for Pyrosequencing in human, mouse, rat ZNF92


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

Entrez Gene cytogenetic band: 7q11.21   Ensembl cytogenetic band:  7q11.21   HGNC cytogenetic band: 7q11.21

ZNF92 Gene in genomic location: bands according to Ensembl, locations according to (and/or Entrez Gene and/or Ensembl if different)
ZNF92 gene location

GeneLoc information about chromosome 7         GeneLoc Exon Structure

GeneLoc location for GC07P064838:  view genomic region     (about GC identifiers)

Start:
64,838,712 bp from pter      End:
64,866,038 bp from pter
Size:
27,327 bases      Orientation:
plus strand

1 alternative location:
Chr7+,CRA_TCAG 64,176,361-64,203,591     

(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, 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., Antibodies by EMD Millipore, R&D Systems, Cell Signaling Technology, OriGene, Novus Biologicals, Thermo Fisher Scientific, LSBio, Abcam, and/or Cloud-Clone Corp.)
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UniProtKB/Swiss-Prot: ZNF92_HUMAN, Q03936 (See protein sequence)
Recommended Name: Zinc finger protein 92  
Size: 586 amino acids; 68487 Da
Developmental stage: Expressed early during embryonic development
Secondary accessions: A6NNF9 Q8N492 Q8NB35
Alternative splicing: 3 isoforms:  Q03936-1   Q03936-2   Q03936-3   (No experimental confirmation available)

Explore the universe of human proteins at neXtProt for ZNF92: NX_Q03936

Explore proteomics data for ZNF92 at MOPED

Post-translational modifications: 

  • Ubiquitination2 at Lys97
  • Modification sites at PhosphoSitePlus

  • See ZNF92 Protein Expression from SPIRE MOPED, PaxDB, and MaxQB

    REFSEQ proteins (5 alternative transcripts): 
    NP_001274461.1  NP_001274462.1  NP_001274463.1  NP_009070.2  NP_689839.1  

    ENSEMBL proteins: 
     ENSP00000332595   ENSP00000400495   ENSP00000396126   ENSP00000350113  
    Reactome Protein details: Q03936

    ZNF92 Human Recombinant Protein Products:

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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 Q03936

    ProtoNet protein and cluster: Q03936

    1 Blocks protein domain: IPB001909 KRAB box

    UniProtKB/Swiss-Prot: ZNF92_HUMAN, Q03936
    Similarity: Belongs to the krueppel C2H2-type zinc-finger protein family
    Similarity: Contains 16 C2H2-type zinc fingers
    Similarity: Contains 1 KRAB domain


    ZNF92 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,
    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, and Vector BioLabs, Cell Lines from GenScript, ESI BIO, In Situ Hybridization Assays from Advanced Cell Diagnostics, Ontologies according to Gene Ontology Consortium 01 Apr 2014 via Entrez Gene.)
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    Molecular Function:

         UniProtKB/Swiss-Prot Summary: ZNF92_HUMAN, Q03936
    Function: May be involved in transcriptional regulation

         Genatlas biochemistry entry for ZNF92:
    zinc finger protein 92 (HTF12),KRAB subfamily

         Gene Ontology (GO): 5 molecular function terms:    About this table

    GO IDQualified GO termEvidencePubMed IDs
    GO:0003676nucleic acid binding ----
    GO:0003677DNA binding IEA--
    GO:0003700sequence-specific DNA binding transcription factor activity NAS2023909
    GO:0008270zinc ion binding NAS2023909
    GO:0046872metal ion binding ----
         
    ZNF92 for ontologies           About GeneDecksing


    Phenotypes:
         1 GenomeRNAi human phenotype for ZNF92:
     Low eccentricity cells 

    Animal Models:
       inGenious Targeting Laboratory: Let us create your new Knockout/Knockin mouse model for ZNF92
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    miRNA
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    miRTarBase miRNAs that target ZNF92:
    hsa-mir-148a-3p (MIRT025985), hsa-mir-361-5p (MIRT020082)

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    (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
    ZNF92_HUMAN, Q03936: Nucleus (Probable)
    Subcellular locations from COMPARTMENTS: 

    CompartmentConfidence
    nucleus5
    cytosol2

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

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

    ZNF92 for ontologies           About GeneDecksing


    (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 ZNF92 About    
    See pathways by source

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

    Pathways by source                                                                                                                                                                 See SuperPaths
    Show all pathways


    1 Reactome Pathway for ZNF92
        Generic Transcription Pathway



    ZNF92 for pathways           About GeneDecksing

        Custom Pathway & Disease-focused RT2 Profiler PCR Arrays for ZNF92
    Interactions:

        Search GeneGlobe Interaction Network for ZNF92

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

    2 Interacting proteins for ZNF92 (Q039363 ENSP000003325954) via UniProtKB, MINT, STRING, and/or I2D
    InteractantInteraction Details
    GeneCardExternal ID(s)
    CREB1P162203, ENSP000003876994I2D: score=1 STRING: ENSP00000387699
    STAT6P422263, ENSP000003001344I2D: score=1 STRING: ENSP00000300134
    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 ----

    ZNF92 for ontologies           About GeneDecksing



    (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 ZNF92



    (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,
    siRNAs from OriGene, QIAGEN, shRNA from OriGene, microRNA from QIAGEN, SwitchGear Genomics,
    Tagged/untagged cDNA clones from OriGene, GenScript, DNA2.0, Vector BioLabs, Primers from OriGene, and/or QIAGEN )
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    REFSEQ mRNAs for ZNF92 gene (5 alternative transcripts): 
    NM_001287532.1  NM_001287533.1  NM_001287534.1  NM_007139.3  NM_152626.3  

    Unigene Cluster for ZNF92:

    Zinc finger protein 92
    Hs.9521  [show with all ESTs]
    Unigene Representative Sequence: NM_152626
    5 Ensembl transcripts including schematic representations, and UCSC links where relevant:
    ENST00000328747(uc003ttz.3 uc003tua.3 uc010kzu.3) ENST00000488849
    ENST00000431504(uc003tub.3) ENST00000450302 ENST00000357512
    miRNA
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    Primer
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      QuantiTect SYBR Green Assays in human, mouse, rat ZNF92
      QuantiFast Probe-based Assays in human, mouse, rat ZNF92

    Additional mRNA sequence: 

    AK091618.1 AK093566.1 BC036439.1 BC040594.1 BX647875.1 M61872.1 

    8 DOTS entries:

    DT.100812409  DT.99975752  DT.210131  DT.95157766  DT.121127724  DT.121127558  DT.91646854  DT.95209034 

    Selected AceView cDNA sequences (see all 47):

    AK091618 CB162419 NM_152626 AI821000 AI469706 BX647875 AX747097 BQ048958 
    BP362173 BC040594 AA329633 BQ423752 NM_007139 BG502050 BP372472 BQ938007 
    AX748205 BC036439 AL598687 BG403184 AA737692 BM724070 BE783397 AI925835 

    GeneLoc Exon Structure

    2 Alternative Splicing Database (ASD) splice patterns (SP) for ZNF92    About this scheme

    ExUns: 1 ^ 2 ^ 3a · 3b
    SP1:                        
    SP2:        -               


    ECgene alternative splicing isoforms for ZNF92

    (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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    ZNF92 expression in normal human tissues (normalized intensities)
    See probesets specificity/sensitivity at GeneAnnot
    About this imageBioGPS <intensity>2/3
    CGAP TAG: TTCAGACTAA
    ZNF92 Expression
    About this image


    ZNF92 expression in embryonic tissues and stem cells    About this table
    Data from LifeMap, the Embryonic Development and Stem Cells Database
     selected tissues (see all 3) fully expand
     
     Epithelial Cells
             Mature Retinal Pigmented Epithelium Cells Retinal Pigmented Epithelium
     
     Eye (Sensory Organs)
             Mature Retinal Pigmented Epithelium Cells Retinal Pigmented Epithelium
     
     Ovary (Reproductive System)
    ZNF92 Protein expression data from MOPED1, PaxDb2 and MaxQB3    About this image

    ZNF92 Protein Expression

    SOURCE GeneReport for Unigene cluster: Hs.9521
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    In Situ
    Assay Products:
     

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

    Orthologs for ZNF92 gene from Selected species (see all 6)    About this table
    Organism Taxonomic
    classification
    Gene Description Human
    Similarity
    Orthology
    Type
    Details
    lizard
    (Anolis carolinensis)
    Reptilia --
    --
    (see all 8)
    Uncharacterized protein
    (see all 8)
    52(a)
    42(a)
    (see all 8)
    many ↔ many
    many ↔ many
    (see all 8)
    AAWZ02037240(11818-13836)
    GL343434.1(292314-296903)
            Species with no ortholog for ZNF92

    ENSEMBL Gene Tree for ZNF92 (if available)
    TreeFam Gene Tree for ZNF92 (if available)

    (Paralogs according to 1HomoloGene,
    2Ensembl, and 3SIMAP, Pseudogenes according to 4Pseudogene.org Build 68)
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    Paralogs for ZNF92 gene
    ZNF852  ZNF4862  ZNF1952  ZNF1002  ZNF7322  ZNF6752  ZNF1382  ZNF5062  
    ZNF662  ZNF2732  ZNF6952  ZNF6262  ZNF6802  ZNF4792  ZNF2532  ZNF932  
    ZNF6822  ZNF4922  ZNF6762  ZNF6812  ZNF1412  ZNF7362  ZNF6792  ZNF2572  
    ZNF2542  ZNF7372  ZNF724P2  ZNF982  ZNF7162  ZNF7142  ZNF4292  ZNF5192  
    ZNF4302  ZNF7302  ZNF1172  ZNF7082  ZNF4312  ZNF902  ZNF7262  ZNF7282  
    Selected SIMAP similar genes for ZNF92 using alignment to 2 protein entries:     ZNF92_HUMAN (see all proteins) (see all similar genes):
    ZNF78L1    ZNF818P    ZNF431    ZNF726    ZFS-1    ZNF429
    ZNF708    ZNF737    ZNF85    ZNF138    ZNF208    ZNF257
    ZNF430    ZNF98    DKFZp686M04222    DKFZp762K012    ZNF479    ZNF716

    ZNF92 for paralogs           About GeneDecksing


    4 Pseudogenes.org Pseudogenes for ZNF92
    PGOHUM00000234246 PGOHUM00000234629 PGOHUM00000234643 PGOHUM00000233685


    (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 ZNF92 (see all 572)    About this table    
    Genomic DataTranscription Related DataAllele Frequencies
    SNP IDValidClinical
    significance
    Chr 7 posSequence#AA
    Chg
    TypeMore#Allele
    freq
    PopTotal
    sample
    More
    ----------
    rs2005683821,2
    --64836793(+) CTGAC-/TCATCT 2 -- us2k10--------
    rs557982221,2
    C,F--64836830(+) GGGTTG/AGGCGC 2 -- us2k13Minor allele frequency- A:0.31NA WA 124
    rs1858028041,2
    --64836846(+) CTCACA/GCCTGT 2 -- us2k10--------
    rs1894143891,2
    --64836850(+) CGCCTA/GTAATC 2 -- us2k10--------
    rs348494401,2
    C,F--64836863(-) CCCAA-/AGTGCT 2 -- us2k12Minor allele frequency- A:0.50NA CSA 4
    rs1923231241,2
    C--64836867(+) CTTTGA/GGAGGC 2 -- us2k10--------
    rs1438120121,2
    C--64836927(+) ACAAGC/GAGAAA 2 -- us2k10--------
    rs1466215311,2
    --64837047(+) GGTTGC/TGGTGA 2 -- us2k10--------
    rs1845341091,2
    --64837062(+) AGATCA/GTGCCA 2 -- us2k10--------
    rs358998511,2
    C--64837095(-) AGTTTC/TGCTCT 2 -- us2k14Minor allele frequency- T:0.12NA WA EA 360

    HapMap Linkage Disequilibrium report for ZNF92 (64838712 - 64866038 bp)

    Structural Variations
         Database of Genomic Variants (DGV) Selected variations for ZNF92 (see all 30):    About this table    
    Variant IDTypeSubtypePubMed ID
    dgv1213e199CNV Deletion23128226
    nsv435849CNV Deletion17901297
    esv2734586CNV Deletion23290073
    dgv1147e201CNV Deletion23290073
    dgv7318n71CNV Loss21882294
    dgv818n27CNV Loss19166990
    nsv831016CNV Loss17160897
    nsv464534CNV Loss19166990
    dgv226e55CNV Loss17911159
    dgv229e55CNV Loss17911159

    Site Specific Mutation Identification with PCR Assays
    SeqTarget long-range PCR primers for resequencing ZNF92
    DNA2.0 Custom Variant and Variant Library Synthesis for ZNF92

    (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.)
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    OMIM gene information: 603974    OMIM disorders: --

    2 diseases for ZNF92:    
    About MalaCards
    myocardial stunning    retinitis

    1 disease from the University of Copenhagen DISEASES database for ZNF92:
    Myocardial stunning

    ZNF92 for disorders           About GeneDecksing

    Genetic Association Database (GAD): ZNF92
    Human Genome Epidemiology (HuGE) Navigator: ZNF92 (4 documents)

    Export disorders for ZNF92 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 ZNF92 gene, integrated from 10 sources (see all 17):
    (articles sorted by number of sources associating them with ZNF92)
        Utopia: connect your pdf to the dynamic
    world of online information

    1. Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score. (PubMed id 20379614)1, 4 Rose J.E....Uhl G.R. (Mol. Med. 2010)
    2. Variation at the NFATC2 locus increases the risk of thiazolidinedione-induced edema in the Diabetes REduction Assessment with ramipril and rosiglitazone Medication (DREAM) study. (PubMed id 20628086)1, 4 Bailey S.D....Anand S. (Diabetes Care 2010)
    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. (Genome Res. 2004)
    4. Complete sequencing and characterization of 21,243 full-length human cDNAs. (PubMed id 14702039)1, 2 Ota T.... Sugano S. (Nat. Genet. 2004)
    5. Clustered organization of homologous KRAB zinc-finger genes with enhanced expression in human T lymphoid cells. (PubMed id 8467795)1, 3 Bellefroid E.J.... Martial J.A. (EMBO J. 1993)
    6. The evolutionarily conserved Kruppel-associated box domain defines a subfamily of eukaryotic multifingered proteins. (PubMed id 2023909)1, 2 Bellefroid E.J....Martial J.A. (Proc. Natl. Acad. Sci. U.S.A. 1991)
    7. 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)
    8. A proteome-wide, quantitative survey of in vivo ubiquitylation sites reveals widespread regulatory roles. (PubMed id 21890473)1 Wagner S.A....Choudhary C. (amp 2011)
    9. An atlas of combinatorial transcriptional regulation in mouse and man. (PubMed id 20211142)1 Ravasi T....Hayashizaki Y. (Cell 2010)
    10. Genome-wide and candidate gene association study of cigarette smoking behaviors. (PubMed id 19247474)4 Caporaso N....Bergen A.W. (PLoS ONE 2009)

    (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)
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    Entrez Gene: 168374 HGNC: 13168 AceView: ZNF92 Ensembl:ENSG00000146757 euGenes: HUgn168374
    ECgene: ZNF92 H-InvDB: ZNF92

    (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 ZNF92 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 ZNF92 gene:
    Search GeneIP for patents involving ZNF92

    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, Gene Editing from DNA2.0. Clones from OriGene, GenScript, Sino Biological, DNA2.0, SwitchGear Genomics, Vector BioLabs, Cell lines from GenScript, and ESI BIO, 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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