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LOC102724768 uncharacterized LOC102724768 [ Homo sapiens (human) ]

Gene ID: 102724768, updated on 10-Dec-2024

Summary

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Gene symbol
LOC102724768
Gene description
uncharacterized LOC102724768
See related
Ensembl:ENSG00000237949
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
Low expression observed in reference dataset See more
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Genomic context

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See LOC102724768 in Genome Data Viewer
Location:
10q21.1
Exon count:
3
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 10 NC_000010.11 (59013682..59066117)
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 10 NC_060934.1 (59867671..59920082)

Chromosome 10 - NC_000010.11Genomic Context describing neighboring genes Neighboring gene RN7SK pseudogene 196 Neighboring gene CDK7 strongly-dependent group 2 enhancer GRCh37_chr10:60679234-60680433 Neighboring gene OCT4-NANOG-H3K4me1 hESC enhancer GRCh37_chr10:60723235-60723736 Neighboring gene OCT4-NANOG-H3K4me1 hESC enhancer GRCh37_chr10:60723737-60724236 Neighboring gene NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr10:60727069-60727982 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 2381 Neighboring gene long intergenic non-protein coding RNA 844 Neighboring gene ribosomal protein lateral stalk subunit P1 pseudogene 10 Neighboring gene TNF receptor associated factor 6 pseudogene 1

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_000010.11 Reference GRCh38.p14 Primary Assembly

    Range
    59013682..59066117
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RNA

  1. XR_428752.5 RNA Sequence

    Related
    ENST00000653466.1

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060934.1 Alternate T2T-CHM13v2.0

    Range
    59867671..59920082
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RNA

  1. XR_007081094.1 RNA Sequence

Nucleotide Protein
Heading Accession and Version

Gene LinkOut

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Other Literature Sources
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Research Materials