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    CTAGE7P CTAGE family member 7, pseudogene [ Homo sapiens (human) ]

    Gene ID: 119437, updated on 17-Jun-2019

    Summary

    Official Symbol
    CTAGE7Pprovided by HGNC
    Official Full Name
    CTAGE family member 7, pseudogeneprovided by HGNC
    Primary source
    HGNC:HGNC:25111
    See related
    Ensembl:ENSG00000233122
    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
    CTAGE7; CTAGEP; rcCTAGE5; bA500G10.2

    Genomic context

    See CTAGE7P in Genome Data Viewer
    Location:
    10q26.3
    Exon count:
    1
    Annotation release Status Assembly Chr Location
    109.20190607 current GRCh38.p13 (GCF_000001405.39) 10 NC_000010.11 (130106009..130108838)
    105 previous assembly GRCh37.p13 (GCF_000001405.25) 10 NC_000010.10 (131904273..131907102)

    Chromosome 10 - NC_000010.11Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC105378558 Neighboring gene EBF transcription factor 3 Neighboring gene VISTA enhancer hs232 Neighboring gene chromosome 10 open reading frame 143 Neighboring gene uncharacterized LOC102724883 Neighboring gene uncharacterized LOC105378561 Neighboring gene glutaredoxin 3

    Genomic regions, transcripts, and products

    Bibliography

    Related articles in PubMed

    GeneRIFs: Gene References Into FunctionsWhat's a GeneRIF?

    General gene information

    Other Names

    • CTAGE family pseudogene
    • CTAGE family, member 5 pseudogene
    • meningioma expressed antigen 6 (coiled-coil proline-rich) pseudogene

    Clone Names

    • MGC33437

    NCBI Reference Sequences (RefSeq)

    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_044994.1 RNA Sequence

      Status: VALIDATED

      Source sequence(s)
      AL139123
      Related
      ENST00000435712.1

    RefSeqs of Annotated Genomes: Homo sapiens Annotation Release 109

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

    Reference GRCh38.p13 Primary Assembly

    Genomic

    1. NC_000010.11 Reference GRCh38.p13 Primary Assembly

      Range
      130106009..130108838
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Suppressed Reference Sequence(s)

    The following Reference Sequences have been suppressed. Explain

    1. NG_006026.3: Suppressed sequence

      Description
      NG_006026.3: This RefSeq was permanently suppressed because it did not represent the correct sequence for the pseudogene (GeneID 119437). A new NG record is provided to represent the genomic region defined by alignment of BC03652
    2. NG_006973.3: Suppressed sequence

      Description
      NG_006973.3: This RefSeq was permanently suppressed because it is now thought that this gene is a transcribed pseudogene.
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