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    LOC100996756 uncharacterized LOC100996756 [ Homo sapiens (human) ]

    Gene ID: 100996756, updated on 10-Dec-2024

    Summary

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    Gene symbol
    LOC100996756
    Gene description
    uncharacterized LOC100996756
    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
    Ubiquitous expression in bone marrow (RPKM 5.7), prostate (RPKM 4.4) and 25 other tissues See more
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    Genomic context

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    See LOC100996756 in Genome Data Viewer
    Location:
    1q21.1
    Exon count:
    2
    Annotation release Status Assembly Chr Location
    RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 1 NC_000001.11 (146386547..146388089)
    RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 1 NC_060925.1 (148420292..148421498, complement)

    Chromosome 1 - NC_000001.11Genomic Context describing neighboring genes Neighboring gene SEC22 homolog B4, pseudogene Neighboring gene tRNA-Asn (anticodon GTT) 24-1 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 1276 Neighboring gene U1 spliceosomal RNA Neighboring gene uncharacterized LOC112268274 Neighboring gene U1 spliceosomal RNA Neighboring gene uncharacterized LOC105371235 Neighboring gene uncharacterized LOC124904407

    Genomic regions, transcripts, and products

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    Go to nucleotide: Graphics FASTA GenBank

    Expression

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    • Project title: Tissue-specific circular RNA induction during human fetal development
    • Description: 35 human fetal samples from 6 tissues (3 - 7 replicates per tissue) collected between 10 and 20 weeks gestational time were sequenced using Illumina TruSeq Stranded Total RNA
    • BioProject: PRJNA270632
    • Publication: PMID 26076956
    • Analysis date: Mon Apr 2 22:54:59 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

    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_000001.11 Reference GRCh38.p14 Primary Assembly

      Range
      146386547..146388089
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    RNA

    1. XR_159169.5 RNA Sequence

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060925.1 Alternate T2T-CHM13v2.0

      Range
      148420292..148421498 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    RNA

    1. XR_007070654.1 RNA Sequence

    Nucleotide Protein
    Heading Accession and Version

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