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    LOC391556 RB binding protein 4, chromatin remodeling factor pseudogene [ Homo sapiens (human) ]

    Gene ID: 391556, updated on 17-Jun-2019

    Summary

    Gene symbol
    LOC391556
    Gene description
    RB binding protein 4, chromatin remodeling factor pseudogene
    Gene type
    pseudo
    RefSeq status
    VALIDATED
    Organism
    Homo sapiens
    Lineage
    Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo

    Genomic context

    See LOC391556 in Genome Data Viewer
    Location:
    3q11.2
    Annotation release Status Assembly Chr Location
    109.20190607 current GRCh38.p13 (GCF_000001405.39) 3 NC_000003.12 (96566295..96567576)
    105 previous assembly GRCh37.p13 (GCF_000001405.25) 3 NC_000003.11 (96285139..96286420)

    Chromosome 3 - NC_000003.12Genomic Context describing neighboring genes Neighboring gene heterogeneous nuclear ribonucleoprotein K pseudogene 4 Neighboring gene microRNA 8060 Neighboring gene RNA, U6 small nuclear 1094, pseudogene Neighboring gene MT-RNR2 like 12

    Genomic regions, transcripts, and products

    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_023232.1 

      Range
      101..1382
      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_000003.12 Reference GRCh38.p13 Primary Assembly

      Range
      96566295..96567576
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)
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