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    LOC101928421 uncharacterized LOC101928421 [ Homo sapiens (human) ]

    Gene ID: 101928421, updated on 9-Jun-2025
    Gene symbol
    LOC101928421
    Gene description
    uncharacterized LOC101928421
    Gene type
    ncRNA
    RefSeq status
    MODEL
    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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    Location:
    7p14.2
    Exon count:
    6
    Annotation release Status Assembly Chr Location
    RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 7 NC_000007.14 (35593993..35631625, complement)
    RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 7 NC_060931.1 (35734907..35772584, complement)

    Chromosome 7 - NC_000007.14Genomic Context describing neighboring genes Neighboring gene VISTA enhancer hs2286 Neighboring gene uncharacterized LOC105375230 Neighboring gene VISTA enhancer hs461 Neighboring gene VISTA enhancer hs472 Neighboring gene VISTA enhancer hs463 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 18095 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr7:35614811-35615311 Neighboring gene uncharacterized LOC124901614 Neighboring gene H3K27ac hESC enhancer GRCh37_chr7:35641191-35641691 Neighboring gene HERPUD family member 2 Neighboring gene MPRA-validated peak6479 silencer Neighboring gene H3K27ac hESC enhancer GRCh37_chr7:35733884-35734771 Neighboring gene HERPUD2 antisense RNA 1

    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 studies and variants in dbVar

    See Variation Viewer (GRCh38)

    NEW Try the new Transcript table

    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_000007.14 Reference GRCh38.p14 Primary Assembly

      Range
      35593993..35631625 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    RNA

    1. XR_007060285.1 RNA Sequence

    2. XR_007060284.1 RNA Sequence

    3. XR_001745169.3 RNA Sequence

    4. XR_927172.4 RNA Sequence

    5. XR_242157.5 RNA Sequence

    6. XR_001745168.3 RNA Sequence

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060931.1 Alternate T2T-CHM13v2.0

      Range
      35734907..35772584 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    RNA

    1. XR_007078405.1 RNA Sequence

    2. XR_007078402.1 RNA Sequence

    3. XR_007078404.1 RNA Sequence

    4. XR_007078401.1 RNA Sequence

    5. XR_007078403.1 RNA Sequence

    6. XR_007078406.1 RNA Sequence

    7. XR_007078400.1 RNA Sequence

    Nucleotide Protein
    Heading Accession and Version

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