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    LOC101928135 uncharacterized LOC101928135 [ Homo sapiens (human) ]

    Gene ID: 101928135, updated on 17-Jun-2024

    Summary

    Gene symbol
    LOC101928135
    Gene description
    uncharacterized LOC101928135
    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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    Genomic context

    See LOC101928135 in Genome Data Viewer
    Location:
    3p22.3
    Exon count:
    4
    Annotation release Status Assembly Chr Location
    RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 3 NC_000003.12 (34875795..35394023, complement)
    RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 3 NC_060927.1 (34876759..35394697, complement)
    105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 3 NC_000003.11 (34917287..35435515, complement)

    Chromosome 3 - NC_000003.12Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC124909365 Neighboring gene ferrochelatase pseudogene 1 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr3:35187219-35187720 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr3:35187721-35188220 Neighboring gene keratin 8 pseudogene 18 Neighboring gene RNA, U6 small nuclear 243, pseudogene Neighboring gene H3K4me1 hESC enhancer GRCh37_chr3:35496170-35496670 Neighboring gene NANOG hESC enhancer GRCh37_chr3:35524036-35524570 Neighboring gene NANOG-H3K4me1 hESC enhancer GRCh37_chr3:35546325-35546826 Neighboring gene NANOG-H3K4me1 hESC enhancer GRCh37_chr3:35546827-35547326 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 19659 Neighboring gene ARPP21 antisense RNA 1 Neighboring gene cAMP regulated phosphoprotein 21 Neighboring gene microRNA 128-2

    Genomic regions, transcripts, and products

    Expression

    • Project title: HPA RNA-seq normal tissues HPA RNA-seq normal tissues
    • Description: RNA-seq was performed of tissue samples from 95 human individuals representing 27 different tissues in order to determine tissue-specificity of all protein-coding genes
    • BioProject: PRJEB4337
    • Publication: PMID 24309898
    • Analysis date: Wed Apr 4 07:08:55 2018

    Phenotypes

    EBI GWAS Catalog

    Description
    Cross-Disorder Genome-Wide Analyses Suggest a Complex Genetic Relationship Between Tourette's Syndrome and OCD.
    EBI GWAS Catalog
    Framingham Heart Study 100K Project: genome-wide associations for blood pressure and arterial stiffness.
    EBI GWAS Catalog
    Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease.
    EBI GWAS Catalog

    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_110817.1 RNA Sequence

      Status: VALIDATED

      Source sequence(s)
      AC092052, BC035904

    RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2023_10

    The following sections contain reference sequences that belong to a specific genome build. Explain

    Reference GRCh38.p14 Primary Assembly

    Genomic

    1. NC_000003.12 Reference GRCh38.p14 Primary Assembly

      Range
      34875795..35394023 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060927.1 Alternate T2T-CHM13v2.0

      Range
      34876759..35394697 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)