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    LOC101060048 uncharacterized LOC101060048 [ Homo sapiens (human) ]

    Gene ID: 101060048, updated on 10-Oct-2023

    Summary

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    Gene symbol
    LOC101060048
    Gene description
    uncharacterized LOC101060048
    Gene type
    pseudo
    RefSeq status
    MODEL
    Organism
    Homo sapiens
    Lineage
    Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
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    Genomic context

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    Location:
    16p11.2
    Annotation release Status Assembly Chr Location
    RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 16 NC_000016.10 (32810719..32812001)
    RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 16 NC_060940.1 (33472671..33473953, complement)

    Chromosome 16 - NC_000016.10Genomic Context describing neighboring genes Neighboring gene COX assembly mitochondrial protein 2 homolog Neighboring gene HERC2 pseudogene 5 Neighboring gene NANOG-H3K27ac hESC enhancer GRCh37_chr16:32832865-32833524 Neighboring gene OCT4 hESC enhancer GRCh37_chr16:32843933-32844434 Neighboring gene NANOG hESC enhancer GRCh37_chr16:32845410-32845911 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr16:32849074-32850050 Neighboring gene ReSE screen-validated silencer GRCh37_chr16:32857908-32858079 Neighboring gene immunoglobulin heavy variable 2/OR16-5 (non-functional) Neighboring gene B cell receptor associated protein 31 pseudogene 2

    Genomic regions, transcripts, and products

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    Go to nucleotide: Graphics FASTA GenBank

    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

    See Variation Viewer (GRCh38)

    NCBI Reference Sequences (RefSeq)

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    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_000016.10 Reference GRCh38.p14 Primary Assembly

      Range
      32810719..32812001
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060940.1 Alternate T2T-CHM13v2.0

      Range
      33472671..33473953 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)
    Nucleotide Protein
    Heading Accession and Version

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