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    LOC105377938 uncharacterized LOC105377938 [ Homo sapiens (human) ]

    Gene ID: 105377938, updated on 17-Sep-2024

    Summary

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    Gene symbol
    LOC105377938
    Gene description
    uncharacterized LOC105377938
    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
    Restricted expression toward bone marrow (RPKM 1.8) See more
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    Genomic context

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    See LOC105377938 in Genome Data Viewer
    Location:
    6q21
    Exon count:
    2
    Annotation release Status Assembly Chr Location
    RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 6 NC_000006.12 (110475517..110479436)
    RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 6 NC_060930.1 (111654016..111657930)

    Chromosome 6 - NC_000006.12Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC105377936 Neighboring gene solute carrier family 22 member 16 Neighboring gene RNA, 7SL, cytoplasmic 617, pseudogene Neighboring gene NANOG hESC enhancer GRCh37_chr6:110776381-110776893 Neighboring gene MPRA-validated peak6024 silencer Neighboring gene OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr6:110832459-110833172 Neighboring gene uncharacterized LOC105377940 Neighboring gene uncharacterized LOC105377939

    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

    General gene information

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    Other Names

    • CTA-331P3.1

    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_000006.12 Reference GRCh38.p14 Primary Assembly

      Range
      110475517..110479436
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    RNA

    1. XR_942860.3 RNA Sequence

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060930.1 Alternate T2T-CHM13v2.0

      Range
      111654016..111657930
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    RNA

    1. XR_007077023.1 RNA Sequence

    Nucleotide Protein
    Heading Accession and Version

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