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    RNY4P15 RNY4 pseudogene 15 [ Homo sapiens (human) ]

    Gene ID: 100379291, updated on 17-Jun-2019

    Summary

    Official Symbol
    RNY4P15provided by HGNC
    Official Full Name
    RNY4 pseudogene 15provided by HGNC
    Primary source
    HGNC:HGNC:34065
    Gene type
    pseudo
    RefSeq status
    INFERRED
    Organism
    Homo sapiens
    Lineage
    Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo

    Genomic context

    See RNY4P15 in Genome Data Viewer
    Location:
    2p11.2
    Annotation release Status Assembly Chr Location
    109.20190607 current GRCh38.p13 (GCF_000001405.39) 2 NC_000002.12 (88229572..88229664, complement)

    Chromosome 2 - NC_000002.12Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC101928347 Neighboring gene fatty acid binding protein 1 Neighboring gene threonine synthase like 2 Neighboring gene mitochondrial ribosomal protein L45 pseudogene 1 Neighboring gene RNA, U6 small nuclear 1168, pseudogene

    Genomic regions, transcripts, and products

    Genomic Sequence:
    NC_000002.12 Chromosome 2 Reference GRCh38.p13 Primary Assembly

    Bibliography

    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_016613.1 

      Range
      101..193
      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_000002.12 Reference GRCh38.p13 Primary Assembly

      Range
      88229572..88229664 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)
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