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    TRIM16L tripartite motif containing 16 like (pseudogene) [ Homo sapiens (human) ]

    Gene ID: 147166, updated on 10-Dec-2024

    Summary

    Official Symbol
    TRIM16Lprovided by HGNC
    Official Full Name
    tripartite motif containing 16 like (pseudogene)provided by HGNC
    Primary source
    HGNC:HGNC:32670
    See related
    Ensembl:ENSG00000291110 AllianceGenome:HGNC:32670
    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
    TRIM70
    Summary
    Predicted to be located in cytoplasm. [provided by Alliance of Genome Resources, Dec 2024]
    Expression
    Ubiquitous expression in esophagus (RPKM 13.7), gall bladder (RPKM 5.6) and 24 other tissues See more
    Orthologs
    NEW
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    Try the new Transcript table

    Genomic context

    See TRIM16L in Genome Data Viewer
    Location:
    17p11.2
    Exon count:
    13
    Annotation release Status Assembly Chr Location
    RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 17 NC_000017.11 (18697998..18736112)
    RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 17 NC_060941.1 (18644447..18682266)
    RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 17 NC_000017.10 (18601311..18639425)

    Chromosome 17 - NC_000017.11Genomic Context describing neighboring genes Neighboring gene H3K27ac hESC enhancer GRCh37_chr17:18553597-18554097 Neighboring gene PAIP1 pseudogene 2 Neighboring gene zinc finger protein 286B (pseudogene) Neighboring gene forkhead box O3B Neighboring gene H3K27ac hESC enhancer GRCh37_chr17:18585117-18585622 Neighboring gene ubiquitin conjugating enzyme E2 S pseudogene 2 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 8279 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr17:18601479-18602036 Neighboring gene OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr17:18621593-18622463 Neighboring gene OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr17:18622464-18623334 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr17:18624898-18625462 Neighboring gene Sharpr-MPRA regulatory region 2370 Neighboring gene F-box and WD repeat domain containing 10 Neighboring gene OCT4-NANOG-H3K4me1 hESC enhancer GRCh37_chr17:18673855-18674355 Neighboring gene trans-golgi network vesicle protein 23 homolog B Neighboring gene NANOG hESC enhancer GRCh37_chr17:18706781-18707432

    Genomic regions, transcripts, and products

    Expression

    • Project title: Tissue-specific circular RNA induction during human fetal development
    • Description: 35 human fetal samples from 6 tissues (3 - 7 replicates per tissue) collected between 10 and 20 weeks gestational time were sequenced using Illumina TruSeq Stranded Total RNA
    • BioProject: PRJNA270632
    • Publication: PMID 26076956
    • Analysis date: Mon Apr 2 22:54:59 2018

    Interactions

    Products Interactant Other Gene Complex Source Pubs Description

    General gene information

    Markers

    Other Names

    • tripartite motif protein 70
    • tripartite motif-containing 16-like
    • tripartite motif-containing protein 16-like protein
    • tripartite motif-containing protein 70

    Gene Ontology Provided by GOA

    Function Evidence Code Pubs
    enables protein binding IPI
    Inferred from Physical Interaction
    more info
    PubMed 
    Component Evidence Code Pubs
    located_in cytoplasm IEA
    Inferred from Electronic Annotation
    more info
     

    NCBI Reference Sequences (RefSeq)

    NEW Try the new Transcript table

    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.

    RNA

    1. NR_172633.1 RNA Sequence

      Status: VALIDATED

      Source sequence(s)
      AC026271, AC107982
    2. NR_172634.1 RNA Sequence

      Status: VALIDATED

      Source sequence(s)
      AC026271, AC107982
      Related
      ENST00000572555.5
    3. NR_172635.1 RNA Sequence

      Status: VALIDATED

      Source sequence(s)
      AC026271, AC107982
    4. NR_172636.1 RNA Sequence

      Status: VALIDATED

      Source sequence(s)
      AC026271
      Related
      ENST00000449697.10
    5. NR_172637.1 RNA Sequence

      Status: VALIDATED

      Source sequence(s)
      AC026271, AC107982
    6. NR_172638.1 RNA Sequence

      Status: VALIDATED

      Source sequence(s)
      AC026271, AC107982
    7. NR_172639.1 RNA Sequence

      Status: VALIDATED

      Source sequence(s)
      AC107982
      Related
      ENST00000571542.6
    8. NR_172640.1 RNA Sequence

      Status: VALIDATED

      Source sequence(s)
      AC107982
      Related
      ENST00000424146.3
    9. NR_172641.1 RNA Sequence

      Status: VALIDATED

      Source sequence(s)
      AC107982
      Related
      ENST00000641936.2

    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_000017.11 Reference GRCh38.p14 Primary Assembly

      Range
      18697998..18736112
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060941.1 Alternate T2T-CHM13v2.0

      Range
      18644447..18682266
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Suppressed Reference Sequence(s)

    The following Reference Sequences have been suppressed. Explain

    1. NM_001037330.3: Suppressed sequence

      Description
      NM_001037330.3: This RefSeq was removed because it is now thought that this gene is a pseudogene.
    2. NM_001353219.2: Suppressed sequence

      Description
      NM_001353219.2: This RefSeq was removed because it is now thought that this gene is a pseudogene.
    3. NM_001353220.2: Suppressed sequence

      Description
      NM_001353220.2: This RefSeq was removed because it is now thought that this gene is a pseudogene.
    4. NM_001353221.2: Suppressed sequence

      Description
      NM_001353221.2: This RefSeq was removed because it is now thought that this gene is a pseudogene.
    5. NM_001353222.2: Suppressed sequence

      Description
      NM_001353222.2: This RefSeq was removed because it is now thought that this gene is a pseudogene.
    6. NM_001353223.2: Suppressed sequence

      Description
      NM_001353223.2: This RefSeq was removed because it is now thought that this gene is a pseudogene.
    7. NM_001353224.2: Suppressed sequence

      Description
      NM_001353224.2: This RefSeq was removed because it is now thought that this gene is a pseudogene.
    8. NM_001353225.2: Suppressed sequence

      Description
      NM_001353225.2: This RefSeq was removed because it is now thought that this gene is a pseudogene.
    9. NM_001353226.2: Suppressed sequence

      Description
      NM_001353226.2: This RefSeq was removed because it is now thought that this gene is a pseudogene.