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    LOC105371300 uncharacterized LOC105371300 [ Homo sapiens (human) ]

    Gene ID: 105371300, updated on 17-Sep-2024

    Summary

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    Gene symbol
    LOC105371300
    Gene description
    uncharacterized LOC105371300
    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 LOC105371300 in Genome Data Viewer
    Location:
    16q21
    Exon count:
    9
    Annotation release Status Assembly Chr Location
    RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 16 NC_000016.10 (59916262..59942774, complement)
    RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 16 NC_060940.1 (65708101..65734607, complement)

    Chromosome 16 - NC_000016.10Genomic Context describing neighboring genes Neighboring gene double homeobox A pseudogene 11 Neighboring gene apolipoprotein O pseudogene 5 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr16:59843104-59843636 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr16:59843637-59844168 Neighboring gene long intergenic non-protein coding RNA 2141 Neighboring gene uncharacterized LOC105371299 Neighboring gene NOP58 ribonucleoprotein homolog (yeast) pseudogene

    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_000016.10 Reference GRCh38.p14 Primary Assembly

      Range
      59916262..59942774 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    RNA

    1. XR_933649.1 RNA Sequence

    2. XR_933648.1 RNA Sequence

    3. XR_933650.1 RNA Sequence

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060940.1 Alternate T2T-CHM13v2.0

      Range
      65708101..65734607 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    RNA

    1. XR_007086674.1 RNA Sequence

    2. XR_007086672.1 RNA Sequence

    3. XR_007086673.1 RNA Sequence

    Nucleotide Protein
    Heading Accession and Version

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