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    TMSB4XP5 TMSB4X pseudogene 5 [ Homo sapiens (human) ]

    Gene ID: 7119, updated on 21-Dec-2019

    Summary

    Official Symbol
    TMSB4XP5provided by HGNC
    Official Full Name
    TMSB4X pseudogene 5provided by HGNC
    Primary source
    HGNC:HGNC:11887
    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
    TMSL5

    Genomic context

    See TMSB4XP5 in Genome Data Viewer
    Location:
    11q12.3
    Annotation release Status Assembly Chr Location
    109.20191205 current GRCh38.p13 (GCF_000001405.39) 11 NC_000011.10 (63520434..63520952, complement)
    105 previous assembly GRCh37.p13 (GCF_000001405.25) 11 NC_000011.9 (63287903..63288424, complement)

    Chromosome 11 - NC_000011.10Genomic Context describing neighboring genes Neighboring gene phospholipase A and acyltransferase 5 Neighboring gene zinc finger protein 91 pseudogene Neighboring gene galectin 12 Neighboring gene Sharpr-MPRA regulatory region 8142 Neighboring gene phospholipase A and acyltransferase 4

    Genomic regions, transcripts, and products

    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_002996.6 

      Range
      101..619
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    RefSeqs of Annotated Genomes: Homo sapiens Updated Annotation Release 109.20191205

    The following sections contain reference sequences that belong to a specific genome build. Explain

    Reference GRCh38.p13 Primary Assembly

    Genomic

    1. NC_000011.10 Reference GRCh38.p13 Primary Assembly

      Range
      63520434..63520952 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)
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