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    LOC101929007 uncharacterized LOC101929007 [ Homo sapiens (human) ]

    Gene ID: 101929007, updated on 10-Dec-2024

    Summary

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    Gene symbol
    LOC101929007
    Gene description
    uncharacterized LOC101929007
    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
    Broad expression in bone marrow (RPKM 1.8), testis (RPKM 1.6) and 19 other tissues See more
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    Genomic context

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    See LOC101929007 in Genome Data Viewer
    Location:
    19p12
    Exon count:
    6
    Annotation release Status Assembly Chr Location
    RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 19 NC_000019.10 (21569902..21594675, complement)
    RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 19 NC_060943.1 (21708389..21733154, complement)

    Chromosome 19 - NC_000019.10Genomic Context describing neighboring genes Neighboring gene zinc finger protein 429 Neighboring gene BCL2 interacting protein 3 pseudogene 26 Neighboring gene H3K27ac hESC enhancer GRCh37_chr19:21734180-21734961 Neighboring gene uncharacterized LOC124904670 Neighboring gene uncharacterized LOC105372323 Neighboring gene Sharpr-MPRA regulatory region 12513 Neighboring gene CPSF6 pseudogene 1 Neighboring gene zinc finger protein 100-like

    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_000019.10 Reference GRCh38.p14 Primary Assembly

      Range
      21569902..21594675 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    RNA

    1. XR_007067176.1 RNA Sequence

    2. XR_002958421.2 RNA Sequence

    3. XR_007067177.1 RNA Sequence

    4. XR_007067179.1 RNA Sequence

    5. XR_001754041.3 RNA Sequence

    6. XR_007067178.1 RNA Sequence

    7. XR_007067180.1 RNA Sequence

    8. XR_001754044.3 RNA Sequence

    9. XR_007067174.1 RNA Sequence

    10. XR_002958423.2 RNA Sequence

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060943.1 Alternate T2T-CHM13v2.0

      Range
      21708389..21733154 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    RNA

    1. XR_007088978.1 RNA Sequence

    2. XR_007088977.1 RNA Sequence

    3. XR_007088979.1 RNA Sequence

    4. XR_007088980.1 RNA Sequence

    5. XR_007088982.1 RNA Sequence

    6. XR_007088981.1 RNA Sequence

    7. XR_007088983.1 RNA Sequence

    8. XR_007088975.1 RNA Sequence

    9. XR_007088976.1 RNA Sequence

    Nucleotide Protein
    Heading Accession and Version

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