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    RPS29P27 ribosomal protein S29 pseudogene 27 [ Homo sapiens (human) ]

    Gene ID: 100271592, updated on 17-Jun-2019

    Summary

    Official Symbol
    RPS29P27provided by HGNC
    Official Full Name
    ribosomal protein S29 pseudogene 27provided by HGNC
    Primary source
    HGNC:HGNC:35836
    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
    RPS29_21_1656

    Genomic context

    See RPS29P27 in Genome Data Viewer
    Location:
    19q13.2
    Annotation release Status Assembly Chr Location
    109.20190607 current GRCh38.p13 (GCF_000001405.39) 19 NC_000019.10 (39697906..39698073)
    105 previous assembly GRCh37.p13 (GCF_000001405.25) 19 NC_000019.9 (40188546..40188713)

    Chromosome 19 - NC_000019.10Genomic Context describing neighboring genes Neighboring gene galectin 16 Neighboring gene galectin 14 pseudogene Neighboring gene galectin 14 Neighboring gene Charcot-Leyden crystal galectin

    Genomic regions, transcripts, and products

    Bibliography

    Related articles in PubMed

    GeneRIFs: Gene References Into FunctionsWhat's a GeneRIF?

    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.

    Genomic

    1. NG_011193.1 

      Range
      101..268
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    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_000019.10 Reference GRCh38.p13 Primary Assembly

      Range
      39697906..39698073
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)
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