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    TVP23BP2 TVP23B pseudogene 2 [ Homo sapiens (human) ]

    Gene ID: 100421473, updated on 17-Jun-2019

    Summary

    Official Symbol
    TVP23BP2provided by HGNC
    Official Full Name
    TVP23B pseudogene 2provided by HGNC
    Primary source
    HGNC:HGNC:38869
    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
    FAM18B4P

    Genomic context

    See TVP23BP2 in Genome Data Viewer
    Location:
    2p13.1
    Annotation release Status Assembly Chr Location
    109.20190607 current GRCh38.p13 (GCF_000001405.39) 2 NC_000002.12 (74628128..74628945, complement)
    105 previous assembly GRCh37.p13 (GCF_000001405.25) 2 NC_000002.11 (74855455..74856069, complement)

    Chromosome 2 - NC_000002.12Genomic Context describing neighboring genes Neighboring gene lysyl oxidase like 3 Neighboring gene docking protein 1 Neighboring gene meiosis 1 associated protein Neighboring gene torsin family 1 member B pseudogene Neighboring gene ssemaphorin 4F Neighboring gene uncharacterized LOC105374808

    Genomic regions, transcripts, and products

    Bibliography

    GeneRIFs: Gene References Into FunctionsWhat's a GeneRIF?

    General gene information

    Other Names

    • family with sequence similarity 18, member B pseudogene
    • family with sequence similarity 18, member B4, pseudogene
    • trans-golgi network vesicle protein 23 homolog B pseudogene 2

    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_023571.2 

      Range
      101..918
      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
      74628128..74628945 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)
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