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    LOC105370109 uncharacterized LOC105370109 [ Homo sapiens (human) ]

    Gene ID: 105370109, updated on 10-Dec-2024

    Summary

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    Gene symbol
    LOC105370109
    Gene description
    uncharacterized LOC105370109
    See related
    Ensembl:ENSG00000262198
    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
    Biased expression in endometrium (RPKM 2.4) and kidney (RPKM 0.3) See more
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    Genomic context

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    See LOC105370109 in Genome Data Viewer
    Location:
    13q12.12
    Exon count:
    3
    Annotation release Status Assembly Chr Location
    RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 13 NC_000013.11 (22884187..22909059)
    RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 13 NC_060937.1 (22083089..22107930)
    RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 13 NC_000013.10 (23458326..23483198)

    Chromosome 13 - NC_000013.11Genomic Context describing neighboring genes Neighboring gene inositol polyphosphate multikinase pseudogene 1 Neighboring gene Rieske (Fe-S) domain containing pseudogene 1 Neighboring gene H3K27ac hESC enhancer GRCh37_chr13:23433285-23434072 Neighboring gene long intergenic non-protein coding RNA 621 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 7448 Neighboring gene NANOG hESC enhancer GRCh37_chr13:23460806-23461307 Neighboring gene BASP1 pseudogene 1 Neighboring gene H3K27ac hESC enhancer GRCh37_chr13:23489315-23490228 Neighboring gene NUS1 pseudogene 2 Neighboring gene collagen alpha-1(III) chain-like

    Genomic regions, transcripts, and products

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    Go to nucleotide: Graphics FASTA GenBank

    Expression

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    • 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

    Bibliography

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    GeneRIFs: Gene References Into Functions

    Phenotypes

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    Review eQTL and phenotype association data in this region using PheGenI

    Variation

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    See variants in ClinVar

    See studies and variants in dbVar

    See Variation Viewer (GRCh37.p13)

    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.

    RNA

    1. NR_187640.1 RNA Sequence

      Status: VALIDATED

      Source sequence(s)
      AL157931, AL162853
      Related
      ENST00000744144.1

    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_000013.11 Reference GRCh38.p14 Primary Assembly

      Range
      22884187..22909059
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060937.1 Alternate T2T-CHM13v2.0

      Range
      22083089..22107930
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)
    Nucleotide Protein
    Heading Accession and Version

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