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    RNF19BPX ring finger protein 19B pseudogene, X-linked [ Homo sapiens (human) ]

    Gene ID: 100419788, updated on 3-Mar-2013
    Official Symbol
    RNF19BPXprovided by HGNC
    Official Full Name
    ring finger protein 19B pseudogene, X-linkedprovided by HGNC
    Primary source
    HGNC:38484
    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
    RNF19BX
    Location :
    chromosome: X
    Sequence :
    Chromosome: X; NC_000023.10 (89463867..89465427, complement)
    See RNF19BPX in Epigenomics, MapViewer

    Chromosome X - NC_000023.10Genomic Context describing neighboring genes Neighboring gene staufen, RNA binding protein, homolog 2 (Drosophila) pseudogene Neighboring gene ubiquitin specific peptidase 12 pseudogene, X-linked Neighboring gene ubiquitin-conjugating enzyme E2 variant 1 pseudogene 9 Neighboring gene TSC22 domain family, member 3 pseudogene

    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_022619.2 Reference

      Range
      101..1661
      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_000023.10 Reference GRCh37.p10 Primary Assembly

      Range
      89463867..89465427, complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate CHM1_1.0

    Genomic

    1. NC_018934.1 Alternate CHM1_1.0

      Range
      89433663..89435222, complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

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