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ZNF182 Gene

protein-coding   GIFtS: 50
GCID: GC0XM047834

Zinc Finger Protein 182

(Previous names: zinc finger protein 182 (HHZ150), zinc finger protein 21...)
(Previous symbol: ZNF21)
  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 1821 2     Zinc Finger Protein 182 (HHZ150)1
ZNF211 2 3 5     HHZ1502
Zinc Finger Protein 21 (KOX 14)1 2     Zfp1822
Zinc Finger Protein KOX142 3     Zinc Finger Protein 213
KOX142 3     

External Ids:    HGNC: 130011   Entrez Gene: 75692   Ensembl: ENSG000001471187   OMIM: 3149935   UniProtKB: P170253   

Export aliases for ZNF182 gene to outside databases

Previous GC identifers: GC00U990427 GC0XM047719 GC0XM045547


(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 ZNF182 Gene:
Zinc-finger proteins bind nucleic acids and play important roles in various cellular functions, including cell
proliferation, differentiation, and apoptosis. This gene encodes a zinc finger protein, and belongs to the
krueppel C2H2-type zinc-finger protein family. It may be involved in transcriptional regulation. Multiple
alternatively spliced transcript variants encoding different isoforms have been identified. (provided by RefSeq,
May 2010)

GeneCards Summary for ZNF182 Gene:
ZNF182 (zinc finger protein 182) is a protein-coding gene. Diseases associated with ZNF182 include aland island eye disease, and eye disease. An important paralog of this gene is ZNF175.

UniProtKB/Swiss-Prot: ZN182_HUMAN, P17025
Function: May be involved in transcriptional regulation

Gene Wiki entry for ZNF182 Gene


(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_000023.11  NC_018934.2  NT_079573.5  
Regulatory elements:
   Regulatory transcription factor binding sites in the ZNF182 gene promoter:
         Nkx3-1   ISGF-3   Nkx3-1 v4   AML1a   Nkx3-1 v1   Evi-1   Nkx3-1 v2   IRF-7A   Nkx3-1 v3   
         Other transcription factors

SwitchGear Promoter luciferase reporter plasmidZNF182 promoter sequence
   Search Chromatin IP Primers for ZNF182

Epigenetics:
DNA Methylation CpG Assay Predesigned for Pyrosequencing in human, mouse, rat ZNF182


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

Entrez Gene cytogenetic band: Xp11.23   Ensembl cytogenetic band:  Xp11.23   HGNC cytogenetic band: Xp11.23

ZNF182 Gene in genomic location: bands according to Ensembl, locations according to (and/or Entrez Gene and/or Ensembl if different)
ZNF182 gene location

GeneLoc information about chromosome X         GeneLoc Exon Structure

GeneLoc location for GC0XM047834:  view genomic region     (about GC identifiers)

Start:
47,834,250 bp from pter      End:
47,863,394 bp from pter
Size:
29,145 bases      Orientation:
minus 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, 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, Cloud-Clone Corp, and/or others.)
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UniProtKB/Swiss-Prot: ZN182_HUMAN, P17025 (See protein sequence)
Recommended Name: Zinc finger protein 182  
Size: 639 amino acids; 73646 Da
Secondary accessions: A2IDD7 Q3KP67 Q96QH7
Alternative splicing: 2 isoforms:  P17025-1   P17025-2   (No experimental confirmation available)

Explore the universe of human proteins at neXtProt for ZNF182: NX_P17025

Explore proteomics data for ZNF182 at MOPED

Post-translational modifications: 

  • Modification sites at neXtProt
  • Modification sites at PhosphoSitePlus

  • See ZNF182 Protein Expression from SPIRE MOPED, PaxDB, and MaxQB

    REFSEQ proteins (3 alternative transcripts): 
    NP_001007089.1  NP_001171570.1  NP_008893.1  

    ENSEMBL proteins: 
     ENSP00000366142   ENSP00000380165   ENSP00000306351  

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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 P17025

    ProtoNet protein and cluster: P17025

    1 Blocks protein domain: IPB001909 KRAB box

    UniProtKB/Swiss-Prot: ZN182_HUMAN, P17025
    Similarity: Belongs to the krueppel C2H2-type zinc-finger protein family
    Similarity: Contains 15 C2H2-type zinc fingers
    Similarity: Contains 1 KRAB domain


    ZNF182 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: ZN182_HUMAN, P17025
    Function: May be involved in transcriptional regulation

         Genatlas biochemistry entry for ZNF182:
    zinc finger 182,C2H2 type,Kruppel-like,Krab subfamily,involved in differentiation and development of heart

         Gene Ontology (GO): 4 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 IBA--
    GO:0046872metal ion binding IEA--
         
    ZNF182 for ontologies           About GeneDecksing


    Phenotypes:
         1 GenomeRNAi human phenotype for ZNF182:
     Decreased p24 protein expressi 

         1 MGI phenotypic allele for Zfp182 (no phenotypes)

    ZNF182 for phenotypes           About GeneDecksing

    Animal Models:
       inGenious Targeting Laboratory: Let us create your new Knockout/Knockin mouse model for ZNF182
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    Selected qRT-PCR Assays for microRNAs that regulate ZNF182 (see all 13):
    hsa-miR-3690 hsa-miR-522 hsa-let-7a-2* hsa-miR-1253 hsa-miR-378b hsa-miR-224* hsa-miR-422a hsa-miR-513b
    SwitchGear 3'UTR luciferase reporter plasmidZNF182 3' UTR sequence
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    Advanced Cell Diagnostics RNAscope RNA in situ hybridization assays for ZNF182


    (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
    ZN182_HUMAN, P17025: Nucleus (Potential)
    Subcellular locations from COMPARTMENTS: 

    CompartmentConfidence
    nucleus3
    cytosol2

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

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

    ZNF182 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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        Custom Pathway & Disease-focused RT2 Profiler PCR Arrays for ZNF182
    Interactions:

        Search GeneGlobe Interaction Network for ZNF182

    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 IBA--

    ZNF182 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 ZNF182 (ZN182)



    (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, Primers from OriGene, and/or QIAGEN )
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    REFSEQ mRNAs for ZNF182 gene (3 alternative transcripts): 
    NM_001007088.1  NM_001178099.1  NM_006962.1  

    Unigene Cluster for ZNF182:

    Zinc finger protein 182
    Hs.189690  [show with all ESTs]
    Unigene Representative Sequence: NM_001178099
    3 Ensembl transcripts including schematic representations, and UCSC links where relevant:
    ENST00000376943 ENST00000396965(uc004dir.3 uc004dis.3 uc004dit.3)
    ENST00000305127
    miRNA
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    Selected qRT-PCR Assays for microRNAs that regulate ZNF182 (see all 13):
    hsa-miR-3690 hsa-miR-522 hsa-let-7a-2* hsa-miR-1253 hsa-miR-378b hsa-miR-224* hsa-miR-422a hsa-miR-513b
    SwitchGear 3'UTR luciferase reporter plasmidZNF182 3' UTR sequence
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      QuantiTect SYBR Green Assays in human, mouse, rat ZNF182
      QuantiFast Probe-based Assays in human, mouse, rat ZNF182

    Additional mRNA sequence: 

    AK097687.1 AK122874.1 AK130362.1 AK299325.1 BC106875.2 BC114216.1 BX537686.1 BX648401.1 
    X52345.1 

    4 DOTS entries:

    DT.104702  DT.207706  DT.121315948  DT.70104709 

    Selected AceView cDNA sequences (see all 49):

    CA435762 BX419699 BX115806 BM722079 AW137383 AA129708 AI733750 AK130362 
    BU618679 AI632919 AW305012 X52345 BU681237 AW440129 BM845671 BF589361 
    BQ006588 BX537686 AA223719 AK097687 AL121500 AI732432 BX096369 AA133309 

    GeneLoc Exon Structure

    3 Alternative Splicing Database (ASD) splice patterns (SP) for ZNF182    About this scheme

    ExUns: 1 ^ 2a · 2b ^ 3
    SP1:              -         
    SP2:              -         
    SP3:                        


    ECgene alternative splicing isoforms for ZNF182

    (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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    ZNF182 expression in normal human tissues (normalized intensities)
    See probesets specificity/sensitivity at GeneAnnot
    About this imageBioGPS <intensity>2/3
    CGAP TAG: AGAACCTGGT
    ZNF182 Expression
    About this image

    ZNF182 Protein expression data from MOPED1, PaxDb2 and MaxQB3    About this image

    ZNF182 Protein Expression

    SOURCE GeneReport for Unigene cluster: Hs.189690
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    In Situ
    Assay Products:
     

     
    Advanced Cell Diagnostics RNAscope RNA in situ hybridization assays for ZNF182

    (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 human and mouse.

    Orthologs for ZNF182 gene from Selected species (see all 7)    About this table
    Organism Taxonomic
    classification
    Gene Description Human
    Similarity
    Orthology
    Type
    Details
    mouse
    (Mus musculus)
    Mammalia Zfp1821 , 5 zinc finger protein 1821, 5 85.7(n)1
    87.79(a)1
      X (16.55 cM)5
    3195351  NM_001111076.11  NP_001104546.11 
     210289395 


    ENSEMBL Gene Tree for ZNF182 (if available)
    TreeFam Gene Tree for ZNF182 (if available)

    (Paralogs according to 1HomoloGene,
    2Ensembl, and 3SIMAP, Pseudogenes according to 4Pseudogene.org Build 68)
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    Paralogs for ZNF182 gene
    ZNF1752  ZNF6742  ZNF4872  ZNF5102  ZIM32  ZNF6142  ZNF1572  ZNF262  
    ZNF6132  ZNF812  ZNF6492  ENSG000002673602  ZNF7822  ZNF7932  ZNF252  ZNF5682  
    ENSG000002365752  ENSG000002296312  ZNF5672  ZNF37A2  ZNF2482  ZNF3002  ZNF3822  RBAK-RBAKDN2  
    Selected SIMAP similar genes for ZNF182 using alignment to 1 protein entry:     ZN182_HUMAN(see all similar genes):
    ZNF78L1    ZNF436    ZNF852    DKFZp666M039    POM121C    ZSCAN16
    ZSCAN2    kr-znf3    DKFZp666C237    ZNF664    DKFZp313M0722    HZF36
    LOC101928664    ZNF22    ZNF24    ZNF323    ZNF572    ZSCAN31

    ZNF182 for paralogs           About GeneDecksing


    1 Pseudogenes.org Pseudogene for ZNF182
    PGOHUM00000243103


    (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 ZNF182 (see all 371)    About this table    
    Genomic DataTranscription Related DataAllele Frequencies
    SNP IDValidClinical
    significance
    Chr X posSequence#AA
    Chg
    TypeMore#Allele
    freq
    PopTotal
    sample
    More
    ----------
    rs1411442971,2
    C--47753379(+) GATTCC/GTGTTT 3 -- ds50010--------
    rs455836351,2
    C--47753515(+) TCAATA/TATTTT 3 -- ds50010--------
    rs1865937841,2
    --47753651(+) ATTCAA/CCAAAA 3 -- ds50010--------
    rs5196091,2
    C--47753793(+) GTACAT/CAGTAC 3 -- ut31 ese31Minor allele frequency- C:0.00NA 2
    rs734912761,2
    C--47753886(+) CCCAAG/AGTAAT 3 -- ut311Minor allele frequency- A:0.50WA 2
    rs1424794711,2
    --47754191(+) ACAAAC/TGCTGC 3 -- ut310--------
    rs1461115121,2
    C--47754250(+) GTACAG/TTCCTA 3 -- ut310--------
    rs115505531,2
    C--47754450(+) CCCACA/GGCTGT 3 -- ut312Minor allele frequency- G:0.00NA 4
    rs1910645461,2
    --47754461(+) TCGTTC/GTTTCT 3 -- ut310--------
    rs1832096111,2
    --47754616(+) TTCTCA/GAGGCC 3 -- ut310--------

    HapMap Linkage Disequilibrium report for ZNF182 (47834250 - 47863394 bp)

    Structural Variations
         Database of Genomic Variants (DGV) Selected variations for ZNF182 (see all 11):    About this table    
    Variant IDTypeSubtypePubMed ID
    nsv6890CNV Loss18451855
    nsv522886CNV Gain19592680
    nsv471601CNV Gain15918152
    esv2752324CNV Gain17911159
    esv25781CNV Gain19812545
    esv32909CNV Gain+Loss17666407
    dgv2443e1CNV Complex17122850
    dgv2444e1CNV Complex17122850
    dgv14n29CNV Complex16826518
    dgv2442e1CNV Complex17122850

    Locus Specific Mutation Databases (LSDB): ZNF182

    Site Specific Mutation Identification with PCR Assays
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    (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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    OMIM gene information: 314993    OMIM disorders: --

    6 diseases for ZNF182:    
    About MalaCards
    aland island eye disease    eye disease    synovial sarcoma    wiskott-aldrich syndrome
    sarcoma    hiv-1


    ZNF182 for disorders           About GeneDecksing

    Genetic Association Database (GAD): ZNF182
    Human Genome Epidemiology (HuGE) Navigator: ZNF182 (1 document)

    Export disorders for ZNF182 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 ZNF182 gene, integrated from 10 sources (see all 12):
    (articles sorted by number of sources associating them with ZNF182)
        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. Localization of a novel zinc finger gene to the human chromosome 7p11.2-p12 by fluorescence in situ hybridization. (PubMed id 8914609)1, 3 Wang R....Liew C.C. (Somat. Cell Mol. Genet. 1996)
    4. Clustered organization of KrA1ppel zinc-finger genes at Xp11.23, flanking a translocation breakpoint at OATL1: a physical map with locus assignments for ZNF21, ZNF41, ZNF81, and ELK1. (PubMed id 8088786)1, 3 Knight J.C....Coleman M.P. (Genomics 1994)
    5. Twenty-seven nonoverlapping zinc finger cDNAs from human T cells map to nine different chromosomes with apparent clustering. (PubMed id 2014798)1, 3 Huebner K....Thiesen H.J. (Am. J. Hum. Genet. 1991)
    6. Multiple genes encoding zinc finger domains are expressed in human T cells. (PubMed id 2288909)1, 2 Thiesen H.-J. (New Biol. 1990)
    7. Pathway Analysis of ChIP-Seq-Based NRF1 Target Genes Suggests a Logical Hypothesis of their Involvement in the Pathogenesis of Neurodegenerative Diseases. (PubMed id 24250222)1 Satoh J....Yamamoto Y. (Gene Regul Syst Bio 2013)
    8. Genetic associations of variants in genes encoding HIV-dependency factors required for HIV-1 infection. (PubMed id 21083371)4 Chinn L.W....O'Brien S.J. (J. Infect. Dis. 2010)
    9. Identification of host proteins required for HIV infection through a functional genomic screen. (PubMed id 18187620)1 Brass A.L....Elledge S.J. (Science 2008)
    10. The DNA sequence of the human X chromosome. (PubMed id 15772651)2 Ross M.T.... Bentley D.R. (Nature 2005)

    (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: 7569 HGNC: 13001 AceView: ZNF21 Ensembl:ENSG00000147118 euGenes: HUgn7569
    ECgene: ZNF182 H-InvDB: ZNF182

    (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)
    About This Section

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    NameDescription
    PharmGKB entry for ZNF182 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 ZNF182 gene:
    Search GeneIP for patents involving ZNF182

    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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