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    LOC105372733 uncharacterized LOC105372733 [ Homo sapiens (human) ]

    Gene ID: 105372733, updated on 17-Sep-2024

    Summary

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    Gene symbol
    LOC105372733
    Gene description
    uncharacterized LOC105372733
    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 testis (RPKM 1.4), adrenal (RPKM 0.7) and 25 other tissues See more
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    Genomic context

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    See LOC105372733 in Genome Data Viewer
    Location:
    21p11.2
    Exon count:
    11
    Annotation release Status Assembly Chr Location
    RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 21 NC_000021.9 (9996066..10119490, complement)
    RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 21 NC_060945.1 (9717587..9732889, complement) , (9609437..9669718, complement)

    Chromosome 21 - NC_000021.9Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC124900471 Neighboring gene uncharacterized LOC105372734 Neighboring gene MPRA-validated peak4341 silencer Neighboring gene CDRT15 pseudogene 8 Neighboring gene NANOG hESC enhancer GRCh37_chr21:11186421-11186922 Neighboring gene eukaryotic translation initiation factor 3 subunit F pseudogene 1

    Genomic regions, transcripts, and products

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    Go to nucleotide: Graphics FASTA GenBank

    Expression

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    • Project title: HPA RNA-seq normal tissues
    • Description: RNA-seq was performed of tissue samples from 95 human individuals representing 27 different tissues in order to determine tissue-specificity of all protein-coding genes
    • BioProject: PRJEB4337
    • Publication: PMID 24309898
    • Analysis date: Wed Apr 4 07:08:55 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

    NCBI Reference Sequences (RefSeq)

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    NEW Try the new Transcript table

    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_000021.9 Reference GRCh38.p14 Primary Assembly

      Range
      9996066..10119490 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    RNA

    1. XR_951173.4 RNA Sequence

    2. XR_951174.4 RNA Sequence

    3. XR_951171.3 RNA Sequence

    4. XR_951170.3 RNA Sequence

    5. XR_951164.3 RNA Sequence

    6. XR_002958652.2 RNA Sequence

    7. XR_001754954.2 RNA Sequence

    8. XR_001754953.2 RNA Sequence

    9. XR_001754952.2 RNA Sequence

    10. XR_951172.2 RNA Sequence

    11. XR_007067819.1 RNA Sequence

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060945.1 Alternate T2T-CHM13v2.0

      Range
      9609437..9669718 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    2. NC_060945.1 Alternate T2T-CHM13v2.0

      Range
      9717587..9732889 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    RNA

    1. XR_007090048.1 RNA Sequence

    2. XR_007090047.1 RNA Sequence

    3. XR_007090046.1 RNA Sequence

    4. XR_007090045.1 RNA Sequence

    5. XR_007090049.1 RNA Sequence

    6. XR_007090050.1 RNA Sequence

    Nucleotide Protein
    Heading Accession and Version

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