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    RPL21P117 ribosomal protein L21 pseudogene 117 [ Homo sapiens (human) ]

    Gene ID: 729241, updated on 4-May-2015
    Official Symbol
    RPL21P117provided by HGNC
    Official Full Name
    ribosomal protein L21 pseudogene 117provided by HGNC
    Primary source
    HGNC:HGNC:35987
    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
    RPL21_53_1439
    See RPL21P117 in Epigenomics, MapViewer
    Location:
    15q22.2
    Annotation release Status Assembly Chr Location
    107 current GRCh38.p2 (GCF_000001405.28) 15 NC_000015.10 (59552572..59553133, complement)
    105 previous assembly GRCh37.p13 (GCF_000001405.25) 15 NC_000015.9 (59844771..59845332, complement)

    Chromosome 15 - NC_000015.10Genomic Context describing neighboring genes Neighboring gene ribosomal protein L7a pseudogene Neighboring gene family with sequence similarity 81, member A Neighboring gene ribosomal protein L21 pseudogene 114 Neighboring gene RNA, 5S ribosomal pseudogene 396 Neighboring gene glucosaminyl (N-acetyl) transferase 3, mucin type

    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.

    Genomic

    1. NG_009622.2 

      Range
      101..662
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    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_000015.10 Reference GRCh38.p2 Primary Assembly

      Range
      59552572..59553133
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate CHM1_1.1

    Genomic

    1. NC_018926.2 Alternate CHM1_1.1

      Range
      59962722..59963283
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)