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    CTAGE3P CTAGE family, member 3, pseudogene [ Homo sapiens (human) ]

    Gene ID: 220112, updated on 26-Feb-2013
    Official Symbol
    CTAGE3Pprovided by HGNC
    Official Full Name
    CTAGE family, member 3, pseudogeneprovided by HGNC
    Primary source
    HGNC:24348
    See related
    MIM:608857
    Gene type
    pseudo
    RefSeq status
    INFERRED
    Organism
    Homo sapiens
    Lineage
    Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
    Also known as
    CTAGE3; CTAGE-3
    Location :
    13q14.3
    Sequence :
    Chromosome: 13; NC_000013.10 (52481956..52484889, complement)
    See CTAGE3P in Epigenomics, MapViewer

    Chromosome 13 - NC_000013.10Genomic Context describing neighboring genes Neighboring gene long intergenic non-protein coding RNA 282 Neighboring gene coiled-coil domain containing 70 Neighboring gene ATPase, Cu++ transporting, beta polypeptide Neighboring gene fatty acid binding protein 5 pseudogene 2 Neighboring gene ALG11, alpha-1,2-mannosyltransferase Neighboring gene UTP14, U3 small nucleolar ribonucleoprotein, homolog C (yeast)

    Related articles in PubMed

    GeneRIFs: Gene References Into Functions What'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.

    Genomic

    1. NG_006514.3 Reference

      Range
      5..2938
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    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_000013.10 Reference GRCh37.p10 Primary Assembly

      Range
      52481956..52484889, complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate HuRef

    Genomic

    1. AC_000145.1 Alternate HuRef

      Range
      33270490..33273418, complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate CHM1_1.0

    Genomic

    1. NC_018924.1 Alternate CHM1_1.0

      Range
      33419345..33422278, complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Suppressed Reference Sequence(s)

    The following Reference Sequences have been suppressed. Explain

    1. NM_172237.1: Suppressed sequence

      Description
      NM_172237.1: This RefSeq was permanently suppressed because it is now thought that this gene is a pseudogene.

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