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    LOC101929050 uncharacterized LOC101929050 [ Homo sapiens (human) ]

    Gene ID: 101929050, updated on 10-Dec-2024

    Summary

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    Gene symbol
    LOC101929050
    Gene description
    uncharacterized LOC101929050
    See related
    Ensembl:ENSG00000232817
    Gene type
    ncRNA
    RefSeq status
    VALIDATED
    Organism
    Homo sapiens
    Lineage
    Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
    Expression
    Restricted expression toward testis (RPKM 3.4) See more
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    Genomic context

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    See LOC101929050 in Genome Data Viewer
    Location:
    7q11.21
    Exon count:
    8
    Annotation release Status Assembly Chr Location
    RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 7 NC_000007.14 (63375703..63394267, complement)
    RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 7 NC_060931.1 (64574452..64593010, complement)
    RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 7 NC_000007.13 (62836081..62854645, complement)

    Chromosome 7 - NC_000007.14Genomic Context describing neighboring genes Neighboring gene solute carrier family 25 member 1 pseudogene Neighboring gene uncharacterized LOC100287704 Neighboring gene long intergenic non-protein coding RNA 3075 Neighboring gene vomeronasal 1 receptor 31 pseudogene Neighboring gene vomeronasal 1 receptor 32 pseudogene Neighboring gene uncharacterized LOC124901641 Neighboring gene uncharacterized LOC100287834 Neighboring gene solute carrier family 25 member 1 pseudogene 2 Neighboring gene vomeronasal 1 receptor 33 pseudogene

    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 variants in ClinVar

    See studies and variants in dbVar

    See Variation Viewer (GRCh37.p13)

    See Variation Viewer (GRCh38)

    NCBI Reference Sequences (RefSeq)

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    RefSeqs maintained independently of Annotated Genomes

    These reference sequences exist independently of genome builds. Explain

    These reference sequences are curated independently of the genome annotation cycle, so their versions may not match the RefSeq versions in the current genome build. Identify version mismatches by comparing the version of the RefSeq in this section to the one reported in Genomic regions, transcripts, and products above.

    RNA

    1. NR_187716.1 RNA Sequence

      Status: VALIDATED

      Source sequence(s)
      AC073188

    2. NR_187717.1 RNA Sequence

      Status: VALIDATED

      Source sequence(s)
      AC073188
      Related
      ENST00000844858.1

    3. NR_187718.1 RNA Sequence

      Status: VALIDATED

      Source sequence(s)
      AC073188

    4. NR_187719.1 RNA Sequence

      Status: VALIDATED

      Source sequence(s)
      AC073188
      Related
      ENST00000844865.1

    5. NR_187720.1 RNA Sequence

      Status: VALIDATED

      Source sequence(s)
      AC073188
      Related
      ENST00000844866.1

    6. NR_187721.1 RNA Sequence

      Status: VALIDATED

      Source sequence(s)
      AC073188
      Related
      ENST00000844867.1

    7. NR_187722.1 RNA Sequence

      Status: VALIDATED

      Source sequence(s)
      AC073188
      Related
      ENST00000844870.1

    8. NR_187723.1 RNA Sequence

      Status: VALIDATED

      Source sequence(s)
      AC073188
      Related
      ENST00000844873.1

    9. NR_187724.1 RNA Sequence

      Status: VALIDATED

      Source sequence(s)
      AC073188

    10. NR_187725.1 RNA Sequence

      Status: VALIDATED

      Source sequence(s)
      AC073188
      Related
      ENST00000844875.1

    11. NR_187726.1 RNA Sequence

      Status: VALIDATED

      Source sequence(s)
      AC073188
      Related
      ENST00000844872.1

    12. NR_187727.1 RNA Sequence

      Status: VALIDATED

      Source sequence(s)
      AC073188
      Related
      ENST00000844876.1

    13. NR_187728.1 RNA Sequence

      Status: VALIDATED

      Source sequence(s)
      AC073188
      Related
      ENST00000844881.1

    14. NR_187729.1 RNA Sequence

      Status: VALIDATED

      Source sequence(s)
      AC073188
      Related
      ENST00000844879.1

    15. NR_187730.1 RNA Sequence

      Status: VALIDATED

      Source sequence(s)
      AC073188
      Related
      ENST00000844882.1

    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_000007.14 Reference GRCh38.p14 Primary Assembly

      Range
      63375703..63394267 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060931.1 Alternate T2T-CHM13v2.0

      Range
      64574452..64593010 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)
    Nucleotide Protein
    Heading Accession and Version

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