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    TRIM51CP tripartite motif-containing 51C, pseudogene [ Homo sapiens (human) ]

    Gene ID: 100130105, updated on 27-Aug-2024

    Summary

    Official Symbol
    TRIM51CPprovided by HGNC
    Official Full Name
    tripartite motif-containing 51C, pseudogeneprovided by HGNC
    Primary source
    HGNC:HGNC:43968
    See related
    Ensembl:ENSG00000249910 AllianceGenome:HGNC:43968
    Gene type
    pseudo
    RefSeq status
    INFERRED
    Organism
    Homo sapiens
    Lineage
    Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
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    Genomic context

    Location:
    11p11.12
    Annotation release Status Assembly Chr Location
    RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 11 NC_000011.10 (48945684..48952068)
    RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 11 NC_060935.1 (49122175..49128560)
    105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 11 NC_000011.9 (48967236..48973620)

    Chromosome 11 - NC_000011.10Genomic Context describing neighboring genes Neighboring gene ANKRD33B pseudogene 2 Neighboring gene tripartite motif containing 48 pseudogene Neighboring gene tripartite motif-containing 51G Neighboring gene tripartite motif containing 53C, pseudogene

    Genomic regions, transcripts, and products

    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_028918.2 

      Range
      101..6485
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      GenBank, FASTA, Sequence Viewer (Graphics)

    RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2024_08

    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
      48945684..48952068
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060935.1 Alternate T2T-CHM13v2.0

      Range
      49122175..49128560
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)