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    LOC101928526 uncharacterized LOC101928526 [ Homo sapiens (human) ]

    Gene ID: 101928526, updated on 10-Dec-2024

    Summary

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    Gene symbol
    LOC101928526
    Gene description
    uncharacterized LOC101928526
    Gene type
    ncRNA
    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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    See LOC101928526 in Genome Data Viewer
    Location:
    2q23.1
    Exon count:
    2
    Annotation release Status Assembly Chr Location
    RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 2 NC_000002.12 (148855086..148859502)
    RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 2 NC_060926.1 (149305458..149309862)

    Chromosome 2 - NC_000002.12Genomic Context describing neighboring genes Neighboring gene H3K27ac hESC enhancer GRCh37_chr2:149402393-149402897 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 12000 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 16620 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 16621 Neighboring gene enhancer of polycomb homolog 2 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr2:149435593-149436192 Neighboring gene Neanderthal introgressed variant-containing enhancer experimental_53210 Neighboring gene ReSE screen-validated silencer GRCh37_chr2:149596595-149596791 Neighboring gene RNA, U2 small nuclear 9, pseudogene Neighboring gene ribosomal protein S20 pseudogene 13 Neighboring gene ubiquitin B pseudogene 3

    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_2024_08

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

    Reference GRCh38.p14 Primary Assembly

    Genomic

    1. NC_000002.12 Reference GRCh38.p14 Primary Assembly

      Range
      148855086..148859502
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    RNA

    1. XR_244868.1 RNA Sequence

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060926.1 Alternate T2T-CHM13v2.0

      Range
      149305458..149309862
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    RNA

    1. XR_007072537.1 RNA Sequence

    Nucleotide Protein
    Heading Accession and Version

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