Format

Send to:

Choose Destination
    • Showing Current items.

    LOC100506974 uncharacterized LOC100506974 [ Homo sapiens (human) ]

    Gene ID: 100506974, updated on 17-Jun-2019

    Summary

    Gene symbol
    LOC100506974
    Gene description
    uncharacterized LOC100506974
    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

    Genomic context

    See LOC100506974 in Genome Data Viewer
    Location:
    17p12
    Exon count:
    6
    Annotation release Status Assembly Chr Location
    109.20190607 current GRCh38.p13 (GCF_000001405.39) 17 NC_000017.11 (13790327..13898625, complement)
    105 previous assembly GRCh37.p13 (GCF_000001405.25) 17 NC_000017.10 (13679945..13695867, complement)

    Chromosome 17 - NC_000017.11Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC105371544 Neighboring gene uncharacterized LOC107985014 Neighboring gene COX10 antisense RNA 1 Neighboring gene CMT1A duplicated region transcript 15 pseudogene 1

    Genomic regions, transcripts, and products

    Expression

    • Project title: 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

    Bibliography

    Related articles in PubMed

    GeneRIFs: Gene References Into FunctionsWhat's a GeneRIF?

    Phenotypes

    NHGRI GWAS Catalog

    Description
    Genome-wide association study of conduct disorder symptomatology.
    NHGRI GWA Catalog

    NCBI Reference Sequences (RefSeq)

    RefSeqs of Annotated Genomes: Homo sapiens Annotation Release 109

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

    Reference GRCh38.p13 Primary Assembly

    Genomic

    1. NC_000017.11 Reference GRCh38.p13 Primary Assembly

      Range
      13790327..13898625 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    RNA

    1. XR_001752796.1 RNA Sequence

    2. XR_001752794.1 RNA Sequence

    3. XR_001752797.1 RNA Sequence

    4. XR_001752795.1 RNA Sequence

    Support Center