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    LOC102723684 uncharacterized LOC102723684 [ Homo sapiens (human) ]

    Gene ID: 102723684, updated on 10-Dec-2024

    Summary

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    Gene symbol
    LOC102723684
    Gene description
    uncharacterized LOC102723684
    See related
    Ensembl:ENSG00000286477
    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
    Restricted expression toward testis (RPKM 1.6) See more
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    Genomic context

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    See LOC102723684 in Genome Data Viewer
    Location:
    7p11.2
    Exon count:
    3
    Annotation release Status Assembly Chr Location
    RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 7 NC_000007.14 (56659149..56675082)
    RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 7 NC_060931.1 (56885584..56901475)

    Chromosome 7 - NC_000007.14Genomic Context describing neighboring genes Neighboring gene tripartite motif containing 60 pseudogene 16 Neighboring gene zinc finger protein 736 pseudogene Neighboring gene uncharacterized LOC105375289 Neighboring gene vomeronasal 1 receptor 26 pseudogene Neighboring gene zinc finger protein 257 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 studies and variants in dbVar

    See Variation Viewer (GRCh38)

    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_000007.14 Reference GRCh38.p14 Primary Assembly

      Range
      56659149..56675082
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    RNA

    1. XR_428154.4 RNA Sequence

      Related
      ENST00000671494.2

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060931.1 Alternate T2T-CHM13v2.0

      Range
      56885584..56901475
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    RNA

    1. XR_007078508.1 RNA Sequence

    Nucleotide Protein
    Heading Accession and Version

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