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    TRIM53BP tripartite motif containing 53B, pseudogene [ Homo sapiens (human) ]

    Gene ID: 642425, updated on 10-Oct-2023

    Summary

    Official Symbol
    TRIM53BPprovided by HGNC
    Official Full Name
    tripartite motif containing 53B, pseudogeneprovided by HGNC
    Primary source
    HGNC:HGNC:37144
    See related
    AllianceGenome:HGNC:37144
    Gene type
    pseudo
    RefSeq status
    VALIDATED
    Organism
    Homo sapiens
    Lineage
    Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
    Also known as
    TRIM53B; TRIM53L; TRIM80P; TRIM53L1
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    Genomic context

    Location:
    11q14.3
    Annotation release Status Assembly Chr Location
    RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 11 NC_000011.10 (89841993..89851264)
    RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 11 NC_060935.1 (89761705..89770970)
    105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 11 NC_000011.9 (89575161..89584432)

    Chromosome 11 - NC_000011.10Genomic Context describing neighboring genes Neighboring gene tripartite motif containing 49 Neighboring gene ANKRD33B pseudogene 7 Neighboring gene tripartite motif containing 64B pseudogene Neighboring gene tripartite motif-containing 51B, pseudogene Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr11:89592843-89593838 Neighboring gene NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr11:89593839-89594834 Neighboring gene ANKRD33B pseudogene 8

    Genomic regions, transcripts, and products

    General gene information

    Other Names

    • tripartite motif containing 80, pseudogene
    • tripartite motif-containing 49 pseudogene
    • tripartite motif-containing 53B

    NCBI Reference Sequences (RefSeq)

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    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_012754.1 

      Range
      101..9372
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2023_10

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

    Reference GRCh38.p14 Primary Assembly

    Genomic

    1. NC_000011.10 Reference GRCh38.p14 Primary Assembly

      Range
      89841993..89851264
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060935.1 Alternate T2T-CHM13v2.0

      Range
      89761705..89770970
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Suppressed Reference Sequence(s)

    The following Reference Sequences have been suppressed. Explain

    1. NM_001146208.1: Suppressed sequence

      Description
      NM_001146208.1: This RefSeq was permanently suppressed because it is now thought that this gene is a pseudogene.