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    LOC105375690 uncharacterized LOC105375690 [ Homo sapiens (human) ]

    Gene ID: 105375690, updated on 9-Jun-2025
    Gene symbol
    LOC105375690
    Gene description
    uncharacterized LOC105375690
    Gene type
    ncRNA
    RefSeq status
    VALIDATED
    Organism
    Homo sapiens
    Lineage
    Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
    Expression
    Low expression observed in reference dataset See more
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    See LOC105375690 in Genome Data Viewer
    Location:
    8q22.3
    Exon count:
    8
    Annotation release Status Assembly Chr Location
    RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 8 NC_000008.11 (103481280..103501910, complement)
    RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 8 NC_060932.1 (104608876..104629509, complement)
    RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 8 NC_000008.10 (104493508..104514138, complement)

    Chromosome 8 - NC_000008.11Genomic Context describing neighboring genes Neighboring gene H3K27ac hESC enhancer GRCh37_chr8:104427001-104427622 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr8:104430836-104431727 Neighboring gene solute carrier family 25 member 32 Neighboring gene DDB1 and CUL4 associated factor 13 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 19459 Neighboring gene Sharpr-MPRA regulatory region 6081 Neighboring gene ReSE screen-validated silencer GRCh37_chr8:104577723-104577885 Neighboring gene mediator complex subunit 21 pseudogene Neighboring gene regulating synaptic membrane exocytosis 2 Neighboring gene prothymosin alpha pseudogene 15

    Go to nucleotide: Graphics FASTA GenBank

    • 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

    GeneRIFs: Gene References Into Functions

    Review eQTL and phenotype association data in this region using PheGenI

    See variants in ClinVar

    See studies and variants in dbVar

    See Variation Viewer (GRCh37.p13)

    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_145697.1 RNA Sequence

      Status: VALIDATED

      Description
      Transcript Variant: This variant (1) represents the longest transcript
      Source sequence(s)
      AC012213

    2. NR_145698.1 RNA Sequence

      Status: VALIDATED

      Source sequence(s)
      AC012213

    3. NR_145699.1 RNA Sequence

      Status: VALIDATED

      Source sequence(s)
      AC012213

    4. NR_145700.1 RNA Sequence

      Status: VALIDATED

      Source sequence(s)
      AC012213

    5. NR_145701.1 RNA Sequence

      Status: VALIDATED

      Source sequence(s)
      AC012213

    6. NR_145702.1 RNA Sequence

      Status: VALIDATED

      Source sequence(s)
      AC012213

    7. NR_145703.1 RNA Sequence

      Status: VALIDATED

      Source sequence(s)
      AC012213

    8. NR_145704.1 RNA Sequence

      Status: VALIDATED

      Source sequence(s)
      AC012213

    9. NR_145705.1 RNA Sequence

      Status: VALIDATED

      Source sequence(s)
      AC012213

    10. NR_145706.1 RNA Sequence

      Status: VALIDATED

      Source sequence(s)
      AC012213

    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_000008.11 Reference GRCh38.p14 Primary Assembly

      Range
      103481280..103501910 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060932.1 Alternate T2T-CHM13v2.0

      Range
      104608876..104629509 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)
    Nucleotide Protein
    Heading Accession and Version

    Gene LinkOut

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