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    LOC107984606 uncharacterized LOC107984606 [ Homo sapiens (human) ]

    Gene ID: 107984606, updated on 17-Sep-2024

    Summary

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    Gene symbol
    LOC107984606
    Gene description
    uncharacterized LOC107984606
    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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    Genomic context

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    See LOC107984606 in Genome Data Viewer
    Location:
    13q33.2
    Exon count:
    6
    Annotation release Status Assembly Chr Location
    RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 13 NC_000013.11 (104753525..104837986, complement)
    RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 13 NC_060937.1 (103974636..104058681, complement)

    Chromosome 13 - NC_000013.11Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC105370340 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr13:105174630-105175130 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr13:105175131-105175631 Neighboring gene uncharacterized LOC107984624 Neighboring gene uncharacterized LOC107984607 Neighboring gene uncharacterized LOC107984608 Neighboring gene uncharacterized LOC105370342 Neighboring gene ribosomal protein L7 pseudogene 45 Neighboring gene uncharacterized LOC105370343

    Genomic regions, transcripts, and products

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    Go to nucleotide: Graphics FASTA GenBank

    Expression

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    • 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

    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 studies and variants in dbVar

    Genotypes

    NCBI Reference Sequences (RefSeq)

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    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
      104753525..104837986 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    RNA

    1. XR_001749995.2 RNA Sequence

    2. XR_007063859.1 RNA Sequence

    3. XR_001749994.2 RNA Sequence

    4. XR_001749993.2 RNA Sequence

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060937.1 Alternate T2T-CHM13v2.0

      Range
      103974636..104058681 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    RNA

    1. XR_007083654.1 RNA Sequence

    2. XR_007083653.1 RNA Sequence

    3. XR_007083652.1 RNA Sequence

    4. XR_007083651.1 RNA Sequence

    Nucleotide Protein
    Heading Accession and Version

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