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    LOC101927798 uncharacterized LOC101927798 [ Homo sapiens (human) ]

    Gene ID: 101927798, updated on 10-Dec-2024

    Summary

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    Gene symbol
    LOC101927798
    Gene description
    uncharacterized LOC101927798
    See related
    Ensembl:ENSG00000253165
    Gene type
    ncRNA
    RefSeq status
    VALIDATED
    Organism
    Homo sapiens
    Lineage
    Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
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    Genomic context

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    See LOC101927798 in Genome Data Viewer
    Location:
    8q24.22
    Exon count:
    3
    Annotation release Status Assembly Chr Location
    RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 8 NC_000008.11 (133775551..133777352, complement)
    RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 8 NC_060932.1 (134899574..134901375, complement)
    RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 8 NC_000008.10 (134787794..134789595, complement)

    Chromosome 8 - NC_000008.11Genomic Context describing neighboring genes Neighboring gene NANOG-H3K27ac hESC enhancer GRCh37_chr8:134770744-134771389 Neighboring gene MT-CO1 pseudogene 49 Neighboring gene MT-ND2 pseudogene 7 Neighboring gene NANOG-H3K27ac hESC enhancer GRCh37_chr8:134781362-134781982 Neighboring gene H3K27ac hESC enhancer GRCh37_chr8:134783441-134783941 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr8:134864388-134864888 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr8:134864889-134865389 Neighboring gene uncharacterized LOC101927822 Neighboring gene OCT4-NANOG-H3K4me1 hESC enhancer GRCh37_chr8:134909490-134909990 Neighboring gene MIA SH3 domain ER export factor 2 pseudogene

    Genomic regions, transcripts, and products

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    Go to nucleotide: Graphics FASTA GenBank

    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)

    See Variation Viewer (GRCh38)

    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_125422.1 RNA Sequence

      Status: VALIDATED

      Source sequence(s)
      AC090821, BC015456
      Related
      ENST00000517380.1

    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_000008.11 Reference GRCh38.p14 Primary Assembly

      Range
      133775551..133777352 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060932.1 Alternate T2T-CHM13v2.0

      Range
      134899574..134901375 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)
    Nucleotide Protein
    Heading Accession and Version

    Gene LinkOut

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