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    ZNF818P zinc finger protein 818, pseudogene [ Homo sapiens (human) ]

    Gene ID: 390963, updated on 26-Feb-2013
    Official Symbol
    ZNF818Pprovided by HGNC
    Official Full Name
    zinc finger protein 818, pseudogeneprovided by HGNC
    Primary source
    HGNC:33265
    See related
    HPRD:13537
    Gene type
    pseudo
    RefSeq status
    VALIDATED
    Organism
    Homo sapiens
    Lineage
    Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
    Also known as
    ZNF818
    Location :
    19q13.42
    Sequence :
    Chromosome: 19; NC_000019.9 (53716227..53719347)
    See ZNF818P in Epigenomics, MapViewer

    Chromosome 19 - NC_000019.9Genomic Context describing neighboring genes Neighboring gene zinc finger protein 665 Neighboring gene zinc finger protein 415 pseudogene Neighboring gene NADH dehydrogenase (ubiquinone) flavoprotein 2 pseudogene 1 Neighboring gene zinc finger protein 677

    Related articles in PubMed

    GeneRIFs: Gene References Into Functions What's a GeneRIF?

    Markers

    Clone Names

    • FLJ46385

    Gene Ontology Provided by GOA

    Function Evidence Code Pubs
    DNA binding IEA
    Inferred from Electronic Annotation
    more info
     
    zinc ion binding IEA
    Inferred from Electronic Annotation
    more info
     
    Process Evidence Code Pubs
    regulation of transcription, DNA-dependent IEA
    Inferred from Electronic Annotation
    more info
     
    transcription, DNA-dependent IEA
    Inferred from Electronic Annotation
    more info
     
    Component Evidence Code Pubs
    nucleus IEA
    Inferred from Electronic Annotation
    more info
     

    RefSeqs maintained independently of Annotated Genomes

    These reference sequences exist independently of genome builds. Explain

    These reference sequences are curated independently of the genome annotation cycle, so their versions may not match the RefSeq versions in the current genome build. Identify version mismatches by comparing the version of the RefSeq in this section to the one reported in Genomic regions, transcripts, and products above.

    RNA

    1. NR_073396.1 RNA Sequence

      Status: VALIDATED

      Source sequence(s)
      AC092070, AK128250, BF908632, BG759674, GD137562

    RefSeqs of Annotated Genomes: Homo sapiens Annotation Release 104

    The following sections contain reference sequences that belong to a specific genome build. Explain

    Reference GRCh37.p10 Primary Assembly

    Genomic

    1. NC_000019.9 Reference GRCh37.p10 Primary Assembly

      Range
      53716227..53719347
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate HuRef

    Genomic

    1. AC_000151.1 Alternate HuRef

      Range
      50037222..50040310
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate CHM1_1.0

    Genomic

    1. NC_018930.1 Alternate CHM1_1.0

      Range
      53876838..53879958
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Suppressed Reference Sequence(s)

    The following Reference Sequences have been suppressed. Explain

    1. NG_008186.1: Suppressed sequence

      Description
      NG_008186.1: This RefSeq was permanently suppressed because it is now thought that this gene is transcribed.
    2. NM_001001675.1: Suppressed sequence

      Description
      NM_001001675.1: This RefSeq was permanently suppressed because currently sufficient data to support this transcript do not exist and the transcript is a nonsense-mediated mRNA decay (NMD) candidate.

      Supplemental Content

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