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    NCOR1P1 nuclear receptor corepressor 1 pseudogene 1 [ Homo sapiens (human) ]

    Gene ID: 149934, updated on 4-May-2015
    Official Symbol
    NCOR1P1provided by HGNC
    Official Full Name
    nuclear receptor corepressor 1 pseudogene 1provided by HGNC
    Primary source
    HGNC:HGNC:16724
    See related
    Ensembl:ENSG00000240108
    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
    C20orf191; bB329D4.2
    See NCOR1P1 in Epigenomics, MapViewer
    Location:
    20p11.1
    Exon count:
    2
    Annotation release Status Assembly Chr Location
    107 current GRCh38.p2 (GCF_000001405.28) 20 NC_000020.11 (26103416..26114041, complement)
    105 previous assembly GRCh37.p13 (GCF_000001405.25) 20 NC_000020.10 (26084052..26094677, complement)

    Chromosome 20 - NC_000020.11Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC100134868 Neighboring gene family with sequence similarity 182, member A Neighboring gene MIR663A host gene Neighboring gene microRNA 663a Neighboring gene protein FRG1-like

    Related articles in PubMed

    GeneRIFs: Gene References Into FunctionsWhat's a GeneRIF?

    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_003678.1 RNA Sequence

      Status: VALIDATED

      Source sequence(s)
      BC132806, EH318080
      Related
      ENST00000478176

    RefSeqs of Annotated Genomes: Homo sapiens Annotation Release 107

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

    Reference GRCh38.p2 Primary Assembly

    Genomic

    1. NC_000020.11 Reference GRCh38.p2 Primary Assembly

      Range
      26103416..26114041
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate CHM1_1.1

    Genomic

    1. NC_018931.2 Alternate CHM1_1.1

      Range
      26084223..26094870
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Suppressed Reference Sequence(s)

    The following Reference Sequences have been suppressed. Explain

    1. NM_001039379.1: Suppressed sequence

      Description
      NM_001039379.1: This RefSeq was permanently suppressed because it is now thought that this gene is a pseudogene.